PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
2660910-1	1989	The enzyme activity of glutathione reductase (NAD(P)H:oxidized-glutathione oxidoreductase, EC 1.6.4.2) incorporated in CTAB/H2O/CHCl3-isooctane (1:1, v/v) reverse micelles has been investigated.	Cetrimonium	119-123	glutathione-disulfide reductase	Homo sapiens	23-44
2605251-8	1989	These observations suggest that the interaction of the negatively charged PS polar group with the positively charged trimethylammonium of DOTMA is sufficient to mediate fusion between the two membranes containing these lipids and that the nature of the zwitterionic phospholipid component of these vesicles is an additional determinant of membrane fusion.	Cetrimonium	117-134	surfactant protein C	Homo sapiens	74-76
2547339-3	1989	When a cetyltrimethylammonium bromide (CETAB) extract of human PMN was electrophoresed in a CETAB polyacrylamide gel and transferred to a nitrocellulose filter, IgG1 class AM MoAbs immunostained only the MPO band of the proteins of the extract.	Cetrimonium	39-44	myeloperoxidase	Homo sapiens	204-207
2818611-1	1989	Bovine liver dihydrofolate reductase has been solubilized in reverse micelles of cationic surfactant cetyltrimethylammonium bromide (CTAB) in isooctane-chloroform (1:1,V/V) mixture.	Cetrimonium	101-131	dihydrofolate reductase	Bos taurus	13-36
2818611-1	1989	Bovine liver dihydrofolate reductase has been solubilized in reverse micelles of cationic surfactant cetyltrimethylammonium bromide (CTAB) in isooctane-chloroform (1:1,V/V) mixture.	Cetrimonium	133-137	dihydrofolate reductase	Bos taurus	13-36
3232318-1	1988	Haemophilus (Actinobacillus) pleuropneumoniae Serotypes 5 and 7 capsular antigens (CA-1) were precipitated from culture supernatants with N-cetyl-N,N,N,-trimethylammonium bromide (Cetavlon).	Cetrimonium	138-178	carbonic anhydrase 1	Mus musculus	83-87
2909744-1	1989	New analogues of platelet activating factor (PAF), in which the phosphate and trimethylammonium moieties were replaced with an acylcarbamoyl moiety and a quaternary cyclic ammonium group, were synthesized.	Cetrimonium	78-95	PCNA clamp associated factor	Rattus norvegicus	17-43
2909744-1	1989	New analogues of platelet activating factor (PAF), in which the phosphate and trimethylammonium moieties were replaced with an acylcarbamoyl moiety and a quaternary cyclic ammonium group, were synthesized.	Cetrimonium	78-95	PCNA clamp associated factor	Rattus norvegicus	45-48
2855257-0	1988	[The effect of reversed micelles of cetyltrimethylammonium bromide on equilibrium constants and kinetics of oxidation-reduction reactions with the participation of cytochrome c].	Cetrimonium	36-66	cytochrome c, somatic	Homo sapiens	164-176
3232318-1	1988	Haemophilus (Actinobacillus) pleuropneumoniae Serotypes 5 and 7 capsular antigens (CA-1) were precipitated from culture supernatants with N-cetyl-N,N,N,-trimethylammonium bromide (Cetavlon).	Cetrimonium	180-188	carbonic anhydrase 1	Mus musculus	83-87
15462961-2	1987	In this article, Kok Wei Yap and Andrew Thompson discuss some of the problems of DNA isolation, stressing the need for a gentle and economical procedure such as CTAB precipitation.	Cetrimonium	161-165	Yes1 associated transcriptional regulator	Homo sapiens	25-28
3398860-5	1988	Bidirectional charge shifts of C5 mobility were observed with the two detergent systems TX-100 + DOC and TX-100 + CTAB.	Cetrimonium	114-118	complement C5	Homo sapiens	31-33
18964582-2	1988	Trace amounts of Co(II) catalysed this chemiluminescent reaction strongly, especially in the presence of the cationic surfactant cetyltrimethylammonium bromide.	Cetrimonium	129-159	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	17-23
2826141-5	1987	In CTAB-reversed micellar solutions, quenching of the Zn-porphyrin cytochrome c triplet state by ferricyanide and methyl viologen was studied.	Cetrimonium	3-7	cytochrome c, somatic	Homo sapiens	67-79
3032796-4	1987	In this study, we characterized the binding of native human neutrophil MPO to A. actinomycetemcomitans by an elution procedure dependent on the cationic detergent cetyltrimethylammonium bromide.	Cetrimonium	163-193	myeloperoxidase	Homo sapiens	71-74
3089281-0	1986	Kinetic, equilibrium and spectroscopic studies on cation association at the active center of acetylcholinesterase: topographic distinction between trimethyl and trimethylammonium sites.	Cetrimonium	161-178	acetylcholinesterase (Cartwright blood group)	Homo sapiens	93-113
3024734-1	1987	Myeloperoxidase and eosinophil peroxidase were separated and purified from rat bone marrow cells using cetyltrimethylammonium bromide as the solubilizer and then with column chromatographies on CM-Sephadex C-50 and Con A-Sepharose.	Cetrimonium	103-133	myeloperoxidase	Rattus norvegicus	0-15
3549752-2	1987	Up to 500 mg of raw insulin could be purified on a Nucleosil C8 analytical column using a methanol-containing phosphate buffer carrier and a cetrimide-containing displacer.	Cetrimonium	141-150	insulin	Bos taurus	20-27
3768404-1	1986	The cationic surfactant, cetyl (hexadecyl) trimethylammonium bromide (CTAB), completely inactivates porcine heart cytoplasmic malate dehydrogenase (L-malate:NAD+ oxidoreductase, EC 1.1.1.37) at concentrations (of surfactant) which do not affect the activity of the mitochondrial isoenzyme.	Cetrimonium	70-74	malic enzyme 1	Homo sapiens	126-146
3768404-1	1986	The cationic surfactant, cetyl (hexadecyl) trimethylammonium bromide (CTAB), completely inactivates porcine heart cytoplasmic malate dehydrogenase (L-malate:NAD+ oxidoreductase, EC 1.1.1.37) at concentrations (of surfactant) which do not affect the activity of the mitochondrial isoenzyme.	Cetrimonium	70-74	hydroxysteroid 17-beta dehydrogenase 6	Homo sapiens	162-176
3783793-7	1986	Eosinophil peroxidase is electrophoretically demonstrable only in the presence of the cationic detergent cetyltrimethyl ammonium bromide (CTAB) and has a spectrophotometric optimum of pH 4.4.	Cetrimonium	105-136	eosinophil peroxidase	Rattus norvegicus	0-21
3783793-7	1986	Eosinophil peroxidase is electrophoretically demonstrable only in the presence of the cationic detergent cetyltrimethyl ammonium bromide (CTAB) and has a spectrophotometric optimum of pH 4.4.	Cetrimonium	138-142	eosinophil peroxidase	Rattus norvegicus	0-21
7201475-3	1982	Platinum complexes are retained on solvent generated anion exchangers, prepared by coating reversed-phase (C-18) supports with a monolayer of hexadecyltrimethylammonium bromide.	Cetrimonium	142-176	Bardet-Biedl syndrome 9	Homo sapiens	107-111
3950913-3	1986	Racemic analogues of platelet activating factor (PAF) in which the methylene bridge separating the phosphate and trimethylammonium moieties is altered in length (7a-f) have been prepared.	Cetrimonium	113-130	PCNA clamp associated factor	Homo sapiens	49-52
3935304-5	1985	A modified medium (mPA-D; addition of cetrimide, omission of sulphapyridine and actidione) was more selective and sufficiently recovered noninjured cells.	Cetrimonium	38-47	paddle	Mus musculus	19-24
6092199-4	1984	Myeloperoxidase was solubilized with hexadecyltrimethylammonium bromide and myeloperoxidase activity was measured with a dianisidine-H2O2 assay.	Cetrimonium	37-71	myeloperoxidase	Rattus norvegicus	0-15
6477964-5	1984	To prove the validity of this kinetic method, the model experiments were carried out with acetylcholinesterase and its inhibitors, phenyltrimethylammonium and trimethylammonium.	Cetrimonium	137-154	acetylcholinesterase	Mus musculus	90-110
7116358-2	1982	The mucin fraction was isolated by precipitation with Cetavlon, and characterized in terms of amino acid and carbohydrate composition.	Cetrimonium	54-62	LOC100508689	Homo sapiens	4-9
6497852-7	1984	Three different additives, quinacrine, p-chloromercuribenzoate and cetyltrimethylammonium bromide, strongly inhibited O2.- generation; they also inhibited the reduction by NADPH of cytochrome b at the same low concentrations.	Cetrimonium	67-97	cytochrome b	Sus scrofa	181-193
6272903-1	1981	Human eosinophils from subjects with or without myeloperoxidase (MPO) deficiency and guinea pig eosinophils are able to decarboxylate L-alanine in the presence of the cationic detergent cetyltrimethylammonium bromide (CTAB) but not in the presence of the nonionic detergent Triton X-100.	Cetrimonium	186-216	myeloperoxidase	Cavia porcellus	48-63
7046573-4	1982	Phosphorylcholine is bound by CRP with much higher affinity than other phosphate monoesters speaking for a second binding site with specificity for the positively charged trimethylammonium group.	Cetrimonium	171-188	C-reactive protein	Homo sapiens	30-33
6276474-2	1982	To completely extract MPO from either neutrophils or skin, hexadecyltrimethylammonium bromide (HTAB) was used to solubilize the enzyme.	Cetrimonium	59-93	myeloperoxidase	Homo sapiens	22-25
6276474-2	1982	To completely extract MPO from either neutrophils or skin, hexadecyltrimethylammonium bromide (HTAB) was used to solubilize the enzyme.	Cetrimonium	95-99	myeloperoxidase	Homo sapiens	22-25
6272903-3	1981	When the non-bromide-containing cationic detergent cetyltrimethylammonium hydroxide (CTAOH) is used instead of CTAB, the eosinophils from MPO-deficient subjects are unable to decarboxylate L-alanine.	Cetrimonium	51-83	myeloperoxidase	Homo sapiens	138-141
6272903-3	1981	When the non-bromide-containing cationic detergent cetyltrimethylammonium hydroxide (CTAOH) is used instead of CTAB, the eosinophils from MPO-deficient subjects are unable to decarboxylate L-alanine.	Cetrimonium	85-90	myeloperoxidase	Homo sapiens	138-141
6265355-7	1981	Under defined conditions (KI, 1.4 mM; H2O2, 0.18 mM; cetyltrimethylammonium bromide, 0.008% [wt/vol]; pH 6), the activity of eosinophil peroxidase could be measured in a mixed granulocyte suspension independently of myeloperoxidase.	Cetrimonium	53-83	eosinophil peroxidase	Homo sapiens	125-146
7197282-2	1981	Treatment of CHO-K1 cells with CTAB or ethanol at concentrations that produce comparable increases of membrane fluidity produce to 2- to 3-fold increase of microsomal membrane cholesterol to phospholipid ratio and a 2- to 3-fold increase of the activity of the rate-limiting enzyme of cholesterol biosynthesis, 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase.	Cetrimonium	31-35	3-hydroxy-3-methylglutaryl-coenzyme A reductase	Cricetulus griseus	311-368
508792-1	1979	An acidic protein fraction with an apparent molecular weight of 34 000 has been isolated from the Cetavlon-treated, mucin-free supernatant of the armadillo submandibular gland 0.01 M NaCl extract.	Cetrimonium	98-106	LOC100508689	Homo sapiens	116-121
6247709-5	1980	Myeloperoxidase was extracted from the leukocytes by dissolution in cetyltrimethyl-ammonium bromide (CETAB).	Cetrimonium	68-99	myeloperoxidase	Homo sapiens	0-15
6247709-5	1980	Myeloperoxidase was extracted from the leukocytes by dissolution in cetyltrimethyl-ammonium bromide (CETAB).	Cetrimonium	101-106	myeloperoxidase	Homo sapiens	0-15
718984-3	1978	In segments containing the pancreatic ducts the total mucin precipitable by cetyltrimethylammonium bromide fell from 80% to 5% in 3 h. At 3 h, chromatography on Sephadex G-100 and Sepharose 4B revealed multiple products, including very small molecular weight fragments deficient in carbohydrate label.	Cetrimonium	76-106	solute carrier family 13 member 2	Rattus norvegicus	54-59
184907-2	1976	Detergent gel electrophoresis showed that purified enterotoxin formed high molecular weight aggregates in the presence of both sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide.	Cetrimonium	160-190	cpe	Clostridium perfringens	51-62
25681-3	1978	After illumination of ROS and digitonin, triton X-100 and CTAB-solubilized rhodopsin, and increase was observed in the number of modified SH-groups.	Cetrimonium	58-62	rhodopsin	Bos taurus	75-84
16910-1	1977	The effects of lysolecithin and hexadecyltrimethylammonium bromide on the structure and stability of apoA-II from human high density lipoprotein have been evalued by circular dichroism and fluorescence measurements.	Cetrimonium	32-66	apolipoprotein A2	Homo sapiens	101-108
191815-2	1977	Spin labels localized either deep in the hydrophobic region or in the aqueous phase are only slowly reduced; however a spin-labeled analogue of the cationic detergent cetyltrimethylammonium bromide that partitions at the interface is rapidly reduced by coupled electron transport.	Cetrimonium	167-197	spindlin 1	Rattus norvegicus	0-4
191815-2	1977	Spin labels localized either deep in the hydrophobic region or in the aqueous phase are only slowly reduced; however a spin-labeled analogue of the cationic detergent cetyltrimethylammonium bromide that partitions at the interface is rapidly reduced by coupled electron transport.	Cetrimonium	167-197	spindlin 1	Rattus norvegicus	119-123
55959-7	1976	Rhodopsin, extracted using cetyltrimethylammonium bromide from pure washed ROS, induced prominent chorio-retinal damage at the dose of 500 mug.	Cetrimonium	27-57	rhodopsin	Bos taurus	0-9
997532-2	1976	The subunit vaccine essentially contained only the proteins of the viral envelope, haemagglutinin and neuraminidase, which had been selectively solubilized by treatment with cetyl trimethylammonium bromide.	Cetrimonium	174-205	neuraminidase 1	Homo sapiens	102-115
177219-1	1976	Micelles of hexadecyl trimethyl ammonium bromide (CTABr) have been investigated with the use of a faty acid spin label and its methyl ester derivative.	Cetrimonium	12-48	spindlin 1	Homo sapiens	108-112
177219-1	1976	Micelles of hexadecyl trimethyl ammonium bromide (CTABr) have been investigated with the use of a faty acid spin label and its methyl ester derivative.	Cetrimonium	50-55	spindlin 1	Homo sapiens	108-112
13782920-0	1960	Inhibition of acetylcholinesterase by cetyltrimethylammonium bromide.	Cetrimonium	38-68	acetylcholinesterase (Cartwright blood group)	Homo sapiens	14-34
1182194-8	1975	However, all ionic and non-ionic detergents studied, sodium deoxycholate, sodium taurocholate, Triton X-100, and cetyltrimethylammonium bromide are capable of inhibiting the rat liver cholesterol esterase in a concentration dependent manner.	Cetrimonium	113-143	carboxyl ester lipase	Rattus norvegicus	184-204
5533197-2	1970	Labelled rhodopsin was also prepared for the first time in cetyltrimethylammonium bromide and purified by column chromatography.	Cetrimonium	59-89	rhodopsin	Homo sapiens	9-18
4312208-0	1969	Effects of cetyltrimethylammonium bromide on catalytic properties of kidney microsomal glucose-6-phosphatase, inorganic pyrophosphate-glucose phosphotransferase and inorganic pyrophosphatase activities.	Cetrimonium	11-41	glucose-6-phosphatase catalytic subunit 1	Homo sapiens	87-108
14235343-0	1964	ACETYLCHOLINESTERASE: TRIMETHYLAMMONIUM-ION INHIBITION OF DEACETYLATION.	Cetrimonium	22-39	acetylcholinesterase (Cartwright blood group)	Homo sapiens	0-20
4776872-1	1973	Insulin, zinc-insulin and iso-insulin were precipitated by cetyltrimethylammonium bromide when the detergent/protein molar ratio was less than 10:1, whereas no precipitation was observed at ratios greater than 10:1.	Cetrimonium	59-89	insulin	Homo sapiens	0-37
5079248-0	1972	Flash bleaching of rhodopsin in cetyltrimethylammonium bromide.	Cetrimonium	32-62	rhodopsin	Homo sapiens	19-28
33560918-7	2021	Altogether, our results indicate that CTAB activates the autophagy-lysosome pathway by inducing the nuclear translocation of TFEB via the inhibition of mTORC1 signaling.	Cetrimonium	38-42	CREB regulated transcription coactivator 1	Mus musculus	152-158
33271277-2	2021	METHODS: Proteinase was ion-paired with benzalkonium chloride (BAK), hexadecylpyridinium chloride (HDP), alkyltrimethylammonium bromide (ATA) and hexadecyltrimethylammonium bromide (HDT) at pH 8.5-9.0, and subsequently incorporated into SEDDS consisting of Cremophor EL, propylene glycol, and Capmul 808-G (40/20/40).	Cetrimonium	146-180	endogenous retrovirus group K member 25	Homo sapiens	9-19
33882231-2	2021	In this work, mica was ultrasonically exfoliated into a single-layered nanomaterial after thermal activation, acidification, sodium replacement, and cetyltrimethylammonium bromide (CTAB) intercalation and then modified with ureido-pyrimidinone (UPy)-based PEG chains.	Cetrimonium	149-179	MHC class I polypeptide-related sequence A	Homo sapiens	14-18
33882231-2	2021	In this work, mica was ultrasonically exfoliated into a single-layered nanomaterial after thermal activation, acidification, sodium replacement, and cetyltrimethylammonium bromide (CTAB) intercalation and then modified with ureido-pyrimidinone (UPy)-based PEG chains.	Cetrimonium	181-185	MHC class I polypeptide-related sequence A	Homo sapiens	14-18
33560918-0	2021	Cetrimonium bromide promotes lipid clearance via TFEB-mediated autophagy-lysosome activation in hepatic cells.	Cetrimonium	0-19	transcription factor EB	Homo sapiens	49-53
33560918-3	2021	Here, we describe that cetrimonium bromide (CTAB), a quaternary ammonium compound, promotes autophagy and lysosomal biogenesis by inducing the nuclear translocation of TFEB in hepatic cells.	Cetrimonium	23-42	transcription factor EB	Homo sapiens	168-172
33560918-3	2021	Here, we describe that cetrimonium bromide (CTAB), a quaternary ammonium compound, promotes autophagy and lysosomal biogenesis by inducing the nuclear translocation of TFEB in hepatic cells.	Cetrimonium	44-48	transcription factor EB	Homo sapiens	168-172
33560918-4	2021	shRNA-mediated TFEB knockdown inhibits CTAB-induced autophagy and lysosomal biogenesis.	Cetrimonium	39-43	transcription factor EB	Homo sapiens	15-19
33560918-5	2021	Mechanistically, CTAB treatment inhibits the Akt-mTORC1 signaling pathway.	Cetrimonium	17-21	AKT serine/threonine kinase 1	Homo sapiens	45-48
33560918-5	2021	Mechanistically, CTAB treatment inhibits the Akt-mTORC1 signaling pathway.	Cetrimonium	17-21	CREB regulated transcription coactivator 1	Mus musculus	49-55
33560918-6	2021	Moreover, CTAB treatment markedly promotes lipid metabolism in both palmitate and oleate-treated HepG2 cells, and this promotion was attenuated by the depletion of TFEB.	Cetrimonium	10-14	transcription factor EB	Homo sapiens	164-168
33560918-7	2021	Altogether, our results indicate that CTAB activates the autophagy-lysosome pathway by inducing the nuclear translocation of TFEB via the inhibition of mTORC1 signaling.	Cetrimonium	38-42	transcription factor EB	Homo sapiens	125-129
34013357-0	2021	The inhibitory effect of CTAB on human osteosarcoma through the PI3K/AKT signaling pathway.	Cetrimonium	25-29	AKT serine/threonine kinase 1	Homo sapiens	69-72
34013357-7	2021	Moreover, CTAB promoted caspase-mediated apoptosis of osteosarcoma cells through the PI3K/AKT cascade, and this effect was accompanied by obvious mitochondrial toxicity.	Cetrimonium	10-14	AKT serine/threonine kinase 1	Homo sapiens	90-93
34013357-9	2021	In conclusion, this study reveals that CTAB has an inhibitory effect on OS by suppressing proliferation and metastasis and inducing apoptosis through the PI3K/AKT signaling pathway and identifies CTAB as a potential therapeutic drug.	Cetrimonium	39-43	AKT serine/threonine kinase 1	Homo sapiens	159-162
34013357-9	2021	In conclusion, this study reveals that CTAB has an inhibitory effect on OS by suppressing proliferation and metastasis and inducing apoptosis through the PI3K/AKT signaling pathway and identifies CTAB as a potential therapeutic drug.	Cetrimonium	196-200	AKT serine/threonine kinase 1	Homo sapiens	159-162
33933799-4	2021	This study focuses on the local structures of Br- in hexadecyltrimethylammonium bromide (HTAB) RMs formed in chloroform and 10% hexanol/heptane.	Cetrimonium	53-87	chromosome 12 open reading frame 73	Homo sapiens	46-48
33933799-4	2021	This study focuses on the local structures of Br- in hexadecyltrimethylammonium bromide (HTAB) RMs formed in chloroform and 10% hexanol/heptane.	Cetrimonium	89-93	chromosome 12 open reading frame 73	Homo sapiens	46-48
33706516-6	2021	In contrast, 19F NMR studies indicated that the quaternary ammonium ion of CTAB interacts with the phenyl group of 3FPBA in the sp2 form via cation-pi interactions.	Cetrimonium	75-79	Sp2 transcription factor	Homo sapiens	128-131
33721170-3	2021	In this study, we use chemical additives such as mannitol, proline, L-arginine and CTAB (cetyl trimethly ammonium bromide) at the recommended concentration during cell lysis to aid in solubility at 37  C. The use of additives resulted in the increased solubility of the recombinant glutathione S-transferase-linked human IRF-1, with L-arginine being most effective.	Cetrimonium	83-87	interferon regulatory factor 1	Homo sapiens	321-326
33297278-6	2021	The addition of Fe3+ and CTAB(cetyl trimethyl ammonium bromide) reagents make the precipitate particles aggregated to flocs(MHA-Fe, MHA-Fe-CTAB) much more large, loose, coarse, and small-density.	Cetrimonium	25-29	myosin heavy chain 9	Homo sapiens	124-127
33303147-4	2021	Employing square-wave stripping mode (after 30 s accumulation at open-circuit condition) in Britton-Robinson buffer, the limits of detection were found to be 1.17 mug mL-1 (2.3 x 10-6 M) for 4 x 10-4 SDS-containing buffer solution at pH 2, and 0.24 mug mL-1 (4.8 x 10-7 M) for 1 x 10-4 CTAB-containing buffer solution at pH 9.0.	Cetrimonium	286-290	L1 cell adhesion molecule	Mus musculus	167-171
33494293-7	2021	For instance, cetyltrimethylammonium bromide showing a superior wetting functionality increased the extent of lysozyme loading more than twice as compared to Tween 80.	Cetrimonium	14-44	lysozyme	Homo sapiens	110-118
33297278-6	2021	The addition of Fe3+ and CTAB(cetyl trimethyl ammonium bromide) reagents make the precipitate particles aggregated to flocs(MHA-Fe, MHA-Fe-CTAB) much more large, loose, coarse, and small-density.	Cetrimonium	25-29	myosin heavy chain 9	Homo sapiens	132-135
33297278-6	2021	The addition of Fe3+ and CTAB(cetyl trimethyl ammonium bromide) reagents make the precipitate particles aggregated to flocs(MHA-Fe, MHA-Fe-CTAB) much more large, loose, coarse, and small-density.	Cetrimonium	30-62	myosin heavy chain 9	Homo sapiens	124-127
33297278-6	2021	The addition of Fe3+ and CTAB(cetyl trimethyl ammonium bromide) reagents make the precipitate particles aggregated to flocs(MHA-Fe, MHA-Fe-CTAB) much more large, loose, coarse, and small-density.	Cetrimonium	30-62	myosin heavy chain 9	Homo sapiens	132-135
33237737-2	2020	Herein, a biodegradable hollow SiO2-based nanosystem (Ag2S-GOx@BHS NYs) is developed by a novel one-step dual-template (bovine serum albumin (BSA) and cetyltrimethylammonium bromide (CTAB)) synthetic strategy for image-guided therapy.	Cetrimonium	151-181	angiotensin II receptor type 1	Homo sapiens	54-58
33237737-2	2020	Herein, a biodegradable hollow SiO2-based nanosystem (Ag2S-GOx@BHS NYs) is developed by a novel one-step dual-template (bovine serum albumin (BSA) and cetyltrimethylammonium bromide (CTAB)) synthetic strategy for image-guided therapy.	Cetrimonium	151-181	hydroxyacid oxidase 1	Homo sapiens	59-62
33237737-2	2020	Herein, a biodegradable hollow SiO2-based nanosystem (Ag2S-GOx@BHS NYs) is developed by a novel one-step dual-template (bovine serum albumin (BSA) and cetyltrimethylammonium bromide (CTAB)) synthetic strategy for image-guided therapy.	Cetrimonium	183-187	angiotensin II receptor type 1	Homo sapiens	54-58
33237737-2	2020	Herein, a biodegradable hollow SiO2-based nanosystem (Ag2S-GOx@BHS NYs) is developed by a novel one-step dual-template (bovine serum albumin (BSA) and cetyltrimethylammonium bromide (CTAB)) synthetic strategy for image-guided therapy.	Cetrimonium	183-187	hydroxyacid oxidase 1	Homo sapiens	59-62
32409040-2	2020	For this purpose, the surface of lipase was initially coated with Triton-X 100 and cetyltrimethylammonium bromide surfactants, to stabilize enzyme in its open form and was then adsorbed onto aminated Fe3O4/SiO2/Gr NC.	Cetrimonium	83-113	lipase	Malus domestica	33-39
32996541-3	2020	In this study, a novel pH-responsive worm-like micelle system was constructed by mixing cetyltrimethylammonium bromide (CTAB), 4-hydroxybenzaldehyde (HB) and p-toluidine (MB) at the molar ratio of 60 mM : 40 mM : 40 mM.	Cetrimonium	88-118	phenylalanine hydroxylase	Homo sapiens	23-25
32996541-3	2020	In this study, a novel pH-responsive worm-like micelle system was constructed by mixing cetyltrimethylammonium bromide (CTAB), 4-hydroxybenzaldehyde (HB) and p-toluidine (MB) at the molar ratio of 60 mM : 40 mM : 40 mM.	Cetrimonium	120-124	phenylalanine hydroxylase	Homo sapiens	23-25
32727781-0	2020	Cetyltrimethylammonium Bromide Disrupts the Mesenchymal Characteristics of HA22T/VGH Cells Via Inactivation of c-Met/PI3K/Akt/mTOR Pathway.	Cetrimonium	0-30	MET proto-oncogene, receptor tyrosine kinase	Homo sapiens	111-116
32727781-0	2020	Cetyltrimethylammonium Bromide Disrupts the Mesenchymal Characteristics of HA22T/VGH Cells Via Inactivation of c-Met/PI3K/Akt/mTOR Pathway.	Cetrimonium	0-30	AKT serine/threonine kinase 1	Homo sapiens	122-125
32727781-0	2020	Cetyltrimethylammonium Bromide Disrupts the Mesenchymal Characteristics of HA22T/VGH Cells Via Inactivation of c-Met/PI3K/Akt/mTOR Pathway.	Cetrimonium	0-30	mechanistic target of rapamycin kinase	Homo sapiens	126-130
32727781-5	2020	In addition, CTAB reduced the levels of metastasis-related proteins including c-Met, phosphoinositide 3-kinase (PI3K), Akt, mammalian target of rapamycin (mTOR), ribosomal protein S6 kinase (p70S6K), Twist, N-cadherin, and Vimentin.	Cetrimonium	13-17	MET proto-oncogene, receptor tyrosine kinase	Homo sapiens	78-83
32727781-5	2020	In addition, CTAB reduced the levels of metastasis-related proteins including c-Met, phosphoinositide 3-kinase (PI3K), Akt, mammalian target of rapamycin (mTOR), ribosomal protein S6 kinase (p70S6K), Twist, N-cadherin, and Vimentin.	Cetrimonium	13-17	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	Homo sapiens	85-110
32727781-5	2020	In addition, CTAB reduced the levels of metastasis-related proteins including c-Met, phosphoinositide 3-kinase (PI3K), Akt, mammalian target of rapamycin (mTOR), ribosomal protein S6 kinase (p70S6K), Twist, N-cadherin, and Vimentin.	Cetrimonium	13-17	AKT serine/threonine kinase 1	Homo sapiens	119-122
32727781-5	2020	In addition, CTAB reduced the levels of metastasis-related proteins including c-Met, phosphoinositide 3-kinase (PI3K), Akt, mammalian target of rapamycin (mTOR), ribosomal protein S6 kinase (p70S6K), Twist, N-cadherin, and Vimentin.	Cetrimonium	13-17	mechanistic target of rapamycin kinase	Homo sapiens	124-153
32727781-5	2020	In addition, CTAB reduced the levels of metastasis-related proteins including c-Met, phosphoinositide 3-kinase (PI3K), Akt, mammalian target of rapamycin (mTOR), ribosomal protein S6 kinase (p70S6K), Twist, N-cadherin, and Vimentin.	Cetrimonium	13-17	mechanistic target of rapamycin kinase	Homo sapiens	155-159
32727781-5	2020	In addition, CTAB reduced the levels of metastasis-related proteins including c-Met, phosphoinositide 3-kinase (PI3K), Akt, mammalian target of rapamycin (mTOR), ribosomal protein S6 kinase (p70S6K), Twist, N-cadherin, and Vimentin.	Cetrimonium	13-17	ribosomal protein S6 kinase B1	Homo sapiens	191-197
32727781-5	2020	In addition, CTAB reduced the levels of metastasis-related proteins including c-Met, phosphoinositide 3-kinase (PI3K), Akt, mammalian target of rapamycin (mTOR), ribosomal protein S6 kinase (p70S6K), Twist, N-cadherin, and Vimentin.	Cetrimonium	13-17	twist family bHLH transcription factor 1	Homo sapiens	200-205
32727781-5	2020	In addition, CTAB reduced the levels of metastasis-related proteins including c-Met, phosphoinositide 3-kinase (PI3K), Akt, mammalian target of rapamycin (mTOR), ribosomal protein S6 kinase (p70S6K), Twist, N-cadherin, and Vimentin.	Cetrimonium	13-17	cadherin 2	Homo sapiens	207-217
32727781-5	2020	In addition, CTAB reduced the levels of metastasis-related proteins including c-Met, phosphoinositide 3-kinase (PI3K), Akt, mammalian target of rapamycin (mTOR), ribosomal protein S6 kinase (p70S6K), Twist, N-cadherin, and Vimentin.	Cetrimonium	13-17	vimentin	Homo sapiens	223-231
32727781-6	2020	Moreover, pretreatment with hepatocyte growth factor (HGF) rescued CTAB-mediated effects.	Cetrimonium	67-71	hepatocyte growth factor	Homo sapiens	28-52
32727781-6	2020	Moreover, pretreatment with hepatocyte growth factor (HGF) rescued CTAB-mediated effects.	Cetrimonium	67-71	hepatocyte growth factor	Homo sapiens	54-57
31088264-3	2020	CTAC enrichment is found to substantially improve Red Mud"s bromate removal ability in comparison to acid activation alone.	Cetrimonium	0-4	adaptor related protein complex 5 subunit mu 1	Homo sapiens	54-57
31088264-5	2020	Maximum CTAC loading is 0.037 g per g acid activated Red Mud (AARM).	Cetrimonium	8-12	adaptor related protein complex 5 subunit mu 1	Homo sapiens	57-60
31088264-7	2020	pH increase is found to adversely affect both AARM and acid activated CTAC enriched Red Mud"s (CTAC-AARM) bromate removal capability, yet CTAC-AARM"s ability proves more resistant to pH changes.	Cetrimonium	70-74	adaptor related protein complex 5 subunit mu 1	Homo sapiens	88-91
33134004-1	2020	We report the synthesis of alpha-Ag2S nanoparticles (NPs) by one-step laser ablation of a silver target in aqueous solution of thiourea (Tu, CH4N2S) mixed with cationic cetyltrimethylammonium bromide (CTAB) as surfactant.	Cetrimonium	169-199	angiotensin II receptor type 1	Homo sapiens	33-37
33134004-1	2020	We report the synthesis of alpha-Ag2S nanoparticles (NPs) by one-step laser ablation of a silver target in aqueous solution of thiourea (Tu, CH4N2S) mixed with cationic cetyltrimethylammonium bromide (CTAB) as surfactant.	Cetrimonium	201-205	angiotensin II receptor type 1	Homo sapiens	33-37
33134004-2	2020	The effect of the CTAB surfactant on the structural, morphological, optical, and elemental composition of Ag2S NPs was evaluated using X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and UV-vis spectroscopy.	Cetrimonium	18-22	angiotensin II receptor type 1	Homo sapiens	106-110
33134004-3	2020	The optical absorption decreased and the optical energy gap of alpha-Ag2S increased from 1.5 to 2 eV after the CTAB surfactant was added to the Tu solution.	Cetrimonium	111-115	angiotensin II receptor type 1	Homo sapiens	69-73
33134004-4	2020	XRD studies revealed that the synthesized Ag2S NPs were polycrystalline with a monoclinic structure and that crystallinity of the nanoparticles was improved after adding CTAB.	Cetrimonium	170-174	angiotensin II receptor type 1	Homo sapiens	42-46
33134004-6	2020	Scanning electron microscopy investigations confirmed the production of monodisperse Ag2S NPs when using the CTAB surfactant.	Cetrimonium	109-113	angiotensin II receptor type 1	Homo sapiens	85-89
32623315-0	2020	Drug affinity to human serum albumin prediction by retention of cetyltrimethylammonium bromide pseudostationary phase in micellar electrokinetic chromatography and chemically advanced template search descriptors.	Cetrimonium	64-94	albumin	Felis catus	29-36
32409040-8	2020	The immobilization yield obtained owing to lipase interfacial activation by Triton X 100 and CTAB was remarkably enhanced by 6-folds and 3-folds, respectively which were remarkably higher in comparison to free immobilized lipase.	Cetrimonium	93-97	lipase	Malus domestica	43-49
32409040-8	2020	The immobilization yield obtained owing to lipase interfacial activation by Triton X 100 and CTAB was remarkably enhanced by 6-folds and 3-folds, respectively which were remarkably higher in comparison to free immobilized lipase.	Cetrimonium	93-97	lipase	Malus domestica	222-228
32079103-1	2020	We have developed a new cationic solid lipid nanoparticle (SLN) formulation, composed of Compritol ATO 888, poloxamer 188 and cetyltrimethylammonium bromide (CTAB), to load perillaldehyde 1,2-epoxide, and surface-tailored with a monoclonal antibody for site-specific targeting of human epithelial growth receptor 2 (HER2).	Cetrimonium	126-156	sarcolipin	Homo sapiens	59-62
32289492-3	2020	Hydrophobic complexes were formed between bovine serum albumin (BSA) and either dodecyl sulfate, cetyl trimethylammonium or 1,2-dipalmitoyl-sn-glycero-3-phosphate applying the organic solvent-free method, Bligh-Dyer method and biphasic metathesis reaction either with ethyl acetate or chloroform as organic phase.	Cetrimonium	97-120	albumin	Homo sapiens	49-62
32231162-2	2020	The syntheses were performed with cetyltrimethylammonium bromide (CTAB) as template in the presence of sodium hydroxide in water at 80  C. The nanomaterials have been characterized by Transmission Electron Microscopy (TEM), nitrogen-sorption measurements (BET), Dynamic Light Scattering (DLS), zeta-potential, Thermogravimetric Analysis (TGA), FTIR, 13C CP MAS NMR and small angle X-ray diffraction (p-XRD).	Cetrimonium	66-70	delta/notch like EGF repeat containing	Homo sapiens	256-259
32079103-1	2020	We have developed a new cationic solid lipid nanoparticle (SLN) formulation, composed of Compritol ATO 888, poloxamer 188 and cetyltrimethylammonium bromide (CTAB), to load perillaldehyde 1,2-epoxide, and surface-tailored with a monoclonal antibody for site-specific targeting of human epithelial growth receptor 2 (HER2).	Cetrimonium	158-162	sarcolipin	Homo sapiens	59-62
31520999-1	2020	In the present study, we report the cooperative refolding/renaturation behaviour of guanidinium hydrochloride (GdnHCl) denatured bovine serum albumin (BSA) in the presence of cationic surfactant cetyltrimethylammonium bromide (CTAB), anionic surfactant sodium dodecyl sulphate (SDS) and their catanionic mixture in the solution of 60 mM sodium phosphate buffer of physiological pH 7.4, using artificial chaperone-assisted two-step method.	Cetrimonium	195-225	albumin	Homo sapiens	136-149
31520999-1	2020	In the present study, we report the cooperative refolding/renaturation behaviour of guanidinium hydrochloride (GdnHCl) denatured bovine serum albumin (BSA) in the presence of cationic surfactant cetyltrimethylammonium bromide (CTAB), anionic surfactant sodium dodecyl sulphate (SDS) and their catanionic mixture in the solution of 60 mM sodium phosphate buffer of physiological pH 7.4, using artificial chaperone-assisted two-step method.	Cetrimonium	227-231	albumin	Homo sapiens	136-149
31550490-4	2019	During preparation, the cetyltrimethylammonium bromide induced the formation of the mesostructured silica layer on the outer surface of CAT/ZIFs.	Cetrimonium	24-54	catalase	Homo sapiens	136-139
31826617-0	2020	Sequestration of Cetyltrimethylammonium Bromide on Gold Nanorods by Human Serum Albumin Causes Its Conformation Change.	Cetrimonium	17-47	albumin	Homo sapiens	74-87
31826617-2	2020	However, the cetyltrimethylammonium bromide (CTAB) surfactant, which is a synthesis byproduct passivating AuNRs to confer colloidal stability, could also cause its conformational change upon interaction with serum albumin during the process of corona formation, thus altering its biological functions.	Cetrimonium	13-43	albumin	Homo sapiens	208-221
31826617-2	2020	However, the cetyltrimethylammonium bromide (CTAB) surfactant, which is a synthesis byproduct passivating AuNRs to confer colloidal stability, could also cause its conformational change upon interaction with serum albumin during the process of corona formation, thus altering its biological functions.	Cetrimonium	45-49	albumin	Homo sapiens	208-221
31402869-0	2019	CTAB Enhances Chemo-Sensitivity Through Activation of AMPK Signaling Cascades in Breast Cancer.	Cetrimonium	0-4	protein kinase AMP-activated catalytic subunit alpha 1	Homo sapiens	54-58
31915438-1	2019	In the present work, the usefulness of cetyltrimethylammonium bromide-modified palm oil fiber (CTAB-modified POF) for the removal of indigo carmine (IC) and 2,6-dichlorophenolindophenol (2,6-DCPIP) from aqueous solutions was investigated.	Cetrimonium	39-69	POF1B actin binding protein	Homo sapiens	109-112
31915438-1	2019	In the present work, the usefulness of cetyltrimethylammonium bromide-modified palm oil fiber (CTAB-modified POF) for the removal of indigo carmine (IC) and 2,6-dichlorophenolindophenol (2,6-DCPIP) from aqueous solutions was investigated.	Cetrimonium	95-99	POF1B actin binding protein	Homo sapiens	109-112
31915438-2	2019	Raw, NaOH-treated, and CTAB-modified POF were characterized by Fourier-transform infrared (FT-IR) spectroscopy, elemental analysis, thermogravimetric-hyperdifferential scanning calorimetric (TG-HDSC) analysis, X-ray diffraction (XRD), and scanning electron microscopy (SEM).	Cetrimonium	23-27	POF1B actin binding protein	Homo sapiens	37-40
31915438-3	2019	The adsorption studies of IC and 2,6-DCPIP were performed in batch mode using CTAB-modified POF.	Cetrimonium	78-82	POF1B actin binding protein	Homo sapiens	92-95
31048243-4	2019	In vitro hemolysis indicated that, among the five copolymers studied, only F127 completely inhibited hemolytic effect of HePC at 50 mug/mL, this effect was also observed for other two amphiphilic molecules (cetyltrimethylammonium bromide and cethylpyridinium chloride).	Cetrimonium	207-237	hepcidin antimicrobial peptide	Homo sapiens	121-125
31417969-0	2019	Potentiometric studies of complex equlibria of CaII, MgII and ZnII with 5-sulphosalicylic acid in cationic micelles of CTAB.	Cetrimonium	119-123	carbonic anhydrase 2	Homo sapiens	47-51
31402869-3	2019	In this study, we hypothesized that AMPK as a key metabolic regulator plays a crucial role in regulation of breast cancer drug resistance, which could be alleviated by treatment of CTAB.	Cetrimonium	181-185	protein kinase AMP-activated catalytic subunit alpha 1	Homo sapiens	36-40
31402869-4	2019	We observed that CTAB can improve the DOX sensitivity of the breast cancer cells by inhibition of the ATP-dependent drug-efflux pump P-gp complex through activation of the AMPK-HIF-1alpha-P-gp cascades.	Cetrimonium	17-21	protein kinase AMP-activated catalytic subunit alpha 1	Homo sapiens	172-176
31402869-6	2019	Taken together, our results showed that CTAB sensitized drug resistance of breast cancer to DOX chemotherapy by activating AMPK signaling cascades both in vitro and in vivo, suggested that CTAB may be developed as a promising and novel chemosensitizer and chemotherapeutic candidate for breast cancer treatment.	Cetrimonium	40-44	protein kinase AMP-activated catalytic subunit alpha 1	Homo sapiens	123-127
31402869-6	2019	Taken together, our results showed that CTAB sensitized drug resistance of breast cancer to DOX chemotherapy by activating AMPK signaling cascades both in vitro and in vivo, suggested that CTAB may be developed as a promising and novel chemosensitizer and chemotherapeutic candidate for breast cancer treatment.	Cetrimonium	189-193	protein kinase AMP-activated catalytic subunit alpha 1	Homo sapiens	123-127
30716549-5	2019	SiO2 adsorbed 85% and 98% CTAB, resulting in concentrations of 2.5 and 0.34 mg/L, mineralized to CO2 >60% within 16 and 23 d, respectively.	Cetrimonium	26-30	complement C2	Homo sapiens	97-100
31187824-5	2019	The impressive chemical nature of CTAB has a synergistic effect in controlling the NGL structure.	Cetrimonium	34-38	erb-b2 receptor tyrosine kinase 2	Homo sapiens	83-86
31187824-6	2019	The cationic head of CTAB and anionic OH- ions resulting from NH4OH ionization have formed a passivating layer that played a profound role in hindering the NGL agglomeration and allowing the NGLs to grow into large lateral dimensions.	Cetrimonium	21-25	erb-b2 receptor tyrosine kinase 2	Homo sapiens	156-159
31943900-1	2019	The effect of a small ionic surfactant, cetyltrimethylammonium bromide (CTAB), on the self-assembly of a beta-peptide has been systematically studied by using scanning electron microscopy, X-ray diffraction, selected area electron diffraction, and molecular dynamics (MD) simulations.	Cetrimonium	40-70	amyloid beta precursor protein	Homo sapiens	103-109
31262888-8	2019	Based on these observations, we suggest that CTAB not only inhibits the canonical transforming growth factor-beta (TGF-beta) signaling pathway though reducing SMADs (an acronym from the fusion of Caenorhabditis elegans Sma genes and the Drosophila Mad, Mothers against decapentaplegic proteins), but also restrains the non-canonical TGF-beta signaling including MAPK pathways like ERK1/2, p38 MAPK, JNK and PI3K.	Cetrimonium	45-49	rolled	Drosophila melanogaster	381-387
31262888-8	2019	Based on these observations, we suggest that CTAB not only inhibits the canonical transforming growth factor-beta (TGF-beta) signaling pathway though reducing SMADs (an acronym from the fusion of Caenorhabditis elegans Sma genes and the Drosophila Mad, Mothers against decapentaplegic proteins), but also restrains the non-canonical TGF-beta signaling including MAPK pathways like ERK1/2, p38 MAPK, JNK and PI3K.	Cetrimonium	45-49	p38b MAP kinase	Drosophila melanogaster	389-397
31262888-8	2019	Based on these observations, we suggest that CTAB not only inhibits the canonical transforming growth factor-beta (TGF-beta) signaling pathway though reducing SMADs (an acronym from the fusion of Caenorhabditis elegans Sma genes and the Drosophila Mad, Mothers against decapentaplegic proteins), but also restrains the non-canonical TGF-beta signaling including MAPK pathways like ERK1/2, p38 MAPK, JNK and PI3K.	Cetrimonium	45-49	basket	Drosophila melanogaster	399-402
31943900-1	2019	The effect of a small ionic surfactant, cetyltrimethylammonium bromide (CTAB), on the self-assembly of a beta-peptide has been systematically studied by using scanning electron microscopy, X-ray diffraction, selected area electron diffraction, and molecular dynamics (MD) simulations.	Cetrimonium	72-76	amyloid beta precursor protein	Homo sapiens	103-109
30601487-0	2019	CTAB-triggered Ag aggregates for reproducible SERS analysis of urinary polycyclic aromatic hydrocarbon metabolites.	Cetrimonium	0-4	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	46-50
30691263-3	2019	For the well-studied system of cationic cetyltrimethylammonium bromide (C16TAB) adsorbed onto the opposite negatively charged, atomically smooth mica surface, a variety of surface aggregates have been previously reported: AFM imaging pointing to cylinders and surface micelles as opposed to mono/bilayer-like structures revealed by neutron and X-ray reflectometry, NMR, spectroscopic techniques, and numerical simulations.	Cetrimonium	40-70	MHC class I polypeptide-related sequence A	Homo sapiens	130-134
30875887-2	2019	Ordered mesoporous silica (MCM-41 type) was synthesized by a surfactant-assisted sol-gel process using tetraethoxysilane as a silica precursor and hexadecyltrimethylammonium bromide as the structure-directing agent.	Cetrimonium	147-181	methylmalonyl-CoA mutase	Homo sapiens	27-30
30601487-1	2019	We propose a novel method for highly sensitive SERS detection of hydrophobic analytes based on cetyltrimethylammonium bromide (CTAB)-triggered Ag aggregates.	Cetrimonium	95-125	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	47-51
30601487-1	2019	We propose a novel method for highly sensitive SERS detection of hydrophobic analytes based on cetyltrimethylammonium bromide (CTAB)-triggered Ag aggregates.	Cetrimonium	127-131	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	47-51
30266011-1	2018	A facile synthesis of hydroxyapatite (HAp) nanoparticles that mimicked biological apatite by utilizing eggshells as a bio-calcium precursor was presented via the hydrothermal method and with the assistance of cetyltrimethylammonium bromide for bone-tissue engineering.	Cetrimonium	209-239	scaffold attachment factor B	Homo sapiens	38-41
29442644-3	2018	Iron-carboxylate MOF (Fe-MOF) was synthesized by the novel cetyltrimethylammonium bromide (CTAB)-citric acid (CA) double-template method.	Cetrimonium	59-89	lysine acetyltransferase 8	Homo sapiens	17-20
30184753-1	2018	A novel magnetic nanocomposite based on magnetite nanoparticles-functionalized-graphene oxide and hexadecyltrimethyl ammonium bromide has been synthesized (MAGO-CTAB) by a facile route for efficient, fast and sensitive binding with Sunset Yellow (SY).	Cetrimonium	98-133	mago homolog B, exon junction complex subunit	Homo sapiens	156-165
30287383-4	2018	In this work, Horseradish peroxidase (HRP) labeled CA 125-antibody (anti-CA 125) was immobilized onto a green and biocompatible nanocomposite containing poly cetyl trimethyl ammonium bromide (P (CTAB) as conductive matrix, chitosan (CS) as biocompatible agent and sliver nanoparticles (Ag NPs) as signal amplification element.	Cetrimonium	195-199	mucin 16, cell surface associated	Homo sapiens	51-57
30287383-4	2018	In this work, Horseradish peroxidase (HRP) labeled CA 125-antibody (anti-CA 125) was immobilized onto a green and biocompatible nanocomposite containing poly cetyl trimethyl ammonium bromide (P (CTAB) as conductive matrix, chitosan (CS) as biocompatible agent and sliver nanoparticles (Ag NPs) as signal amplification element.	Cetrimonium	195-199	mucin 16, cell surface associated	Homo sapiens	73-79
29884355-3	2018	In this work, the DNA1with rich G bases was firstly conjugated on the surfaces of Au NPs fixed on the hexadecyl trimethylammonium bromide (CTAB)-coated glass slide, and thrombin was captured by the DNA1.	Cetrimonium	102-137	coagulation factor II, thrombin	Homo sapiens	169-177
29884355-3	2018	In this work, the DNA1with rich G bases was firstly conjugated on the surfaces of Au NPs fixed on the hexadecyl trimethylammonium bromide (CTAB)-coated glass slide, and thrombin was captured by the DNA1.	Cetrimonium	139-143	coagulation factor II, thrombin	Homo sapiens	169-177
30261640-1	2018	In this study a cationic surfactant, cetyltrimethylammonium bromide (CTAB), was used as a soft template for in situ chemical polymerization of aniline on the surface of microcrystalline cellulose (MCC).	Cetrimonium	37-67	MCC regulator of WNT signaling pathway	Homo sapiens	197-200
30261640-1	2018	In this study a cationic surfactant, cetyltrimethylammonium bromide (CTAB), was used as a soft template for in situ chemical polymerization of aniline on the surface of microcrystalline cellulose (MCC).	Cetrimonium	69-73	MCC regulator of WNT signaling pathway	Homo sapiens	197-200
30261640-5	2018	The overlapping characteristic peaks of pure PAni and MCC caused peak broadening at 3263 cm-1 in the IR spectra of PAni/MCC/CTAB nanocomposite that revealed the interaction between NH of PAni and OH group of MCC via electrostatic interactions.	Cetrimonium	124-128	MCC regulator of WNT signaling pathway	Homo sapiens	54-57
30261640-5	2018	The overlapping characteristic peaks of pure PAni and MCC caused peak broadening at 3263 cm-1 in the IR spectra of PAni/MCC/CTAB nanocomposite that revealed the interaction between NH of PAni and OH group of MCC via electrostatic interactions.	Cetrimonium	124-128	MCC regulator of WNT signaling pathway	Homo sapiens	120-123
30261640-5	2018	The overlapping characteristic peaks of pure PAni and MCC caused peak broadening at 3263 cm-1 in the IR spectra of PAni/MCC/CTAB nanocomposite that revealed the interaction between NH of PAni and OH group of MCC via electrostatic interactions.	Cetrimonium	124-128	MCC regulator of WNT signaling pathway	Homo sapiens	120-123
29442644-3	2018	Iron-carboxylate MOF (Fe-MOF) was synthesized by the novel cetyltrimethylammonium bromide (CTAB)-citric acid (CA) double-template method.	Cetrimonium	59-89	lysine acetyltransferase 8	Homo sapiens	25-28
29442644-3	2018	Iron-carboxylate MOF (Fe-MOF) was synthesized by the novel cetyltrimethylammonium bromide (CTAB)-citric acid (CA) double-template method.	Cetrimonium	91-95	lysine acetyltransferase 8	Homo sapiens	17-20
29442644-3	2018	Iron-carboxylate MOF (Fe-MOF) was synthesized by the novel cetyltrimethylammonium bromide (CTAB)-citric acid (CA) double-template method.	Cetrimonium	91-95	lysine acetyltransferase 8	Homo sapiens	25-28
29308473-13	2018	Specifically, CTAB-nanourchins caused a significant increase in the abundance of Rock1.	Cetrimonium	14-18	Rho associated coiled-coil containing protein kinase 1	Homo sapiens	81-86
29600849-1	2018	We developed a new method by enclosing the complex tris(2-phenylpyridinato-N,C2")Iridium(III), Ir(ppy)3 with surfactant cetyltrimethylammonium bromide (CATB), coated with a thin layer of silica then bonded to the surface of silver nanoparticle.	Cetrimonium	120-150	cathepsin B	Homo sapiens	152-156
29127825-4	2018	Cetyltrimethylammonium bromide-based surfactants with different hydrocarbon lengths and headgroup structures were studied for their structural effects on [Co(I)(bipyridine)3]+-mediated dechlorination reactions.	Cetrimonium	0-30	mitochondrially encoded cytochrome c oxidase I	Homo sapiens	155-160
29667814-1	2018	We obtained a kerosene-soluble form of the lithium salt [UO2(O2)(OH)2]24 phase (Li-U24), by adding cetyltrimethylammonium bromide surfactant to aqueous Li-U24.	Cetrimonium	99-129	small nucleolar RNA, C/D box 24	Homo sapiens	83-86
29308473-15	2018	In addition, CTAB-nanourchins led to a marked decline in pro-survival signaling via the PI3 kinase-Akt pathway.	Cetrimonium	13-17	AKT serine/threonine kinase 1	Homo sapiens	99-102
29096140-2	2018	The four modification methods including the processes of washing with seawater (B), acid treatment Bauxsol (ATB), activated ATB using ammonia (ABA), and activated Bauxsol using cetyltrimethylammonium bromide (CTAB) (ABC) were evaluated to increase the reactivity of red mud (RM) for ferricyanide removal.	Cetrimonium	177-207	ATP binding cassette subfamily B member 6 (Langereis blood group)	Homo sapiens	216-219
28622544-5	2017	In this present work, we have studied the interaction of kappa-casein with cetyltrimethyl ammonium bromide (CTAB), a positively charged surfactant, utilizing various steady state fluorescence, time-resolved fluorescence and circular dichroism spectroscopy.	Cetrimonium	75-106	casein kappa	Homo sapiens	57-69
28987891-4	2017	Cetyl trimethylammonium bromide (CTAB) and sodium dodecyl sulfate (SDS) were employed for CGA creation.	Cetrimonium	0-31	chromogranin A	Homo sapiens	90-93
28987891-4	2017	Cetyl trimethylammonium bromide (CTAB) and sodium dodecyl sulfate (SDS) were employed for CGA creation.	Cetrimonium	33-37	chromogranin A	Homo sapiens	90-93
29025673-6	2018	The date from EDS, FTIR and TGA suggested that the CTAB capped on the surface of CTAB-IONPs, while XRD showed that zero-valent iron and iron oxide were formed.	Cetrimonium	81-85	T-box transcription factor 1	Homo sapiens	28-31
29436987-4	2018	METHODS: Interaction of the anionic Sodium Dodecyl Sulphate (SDS) and the Cationic Cetyltrimethylammonium Bromide (CTAB) surfactants with domain III of Human Serum Albumin (HSA) has been studied using 8-Anilino-1-Naphthalene-Sulphonate (ANS) as a fluorescent marker.	Cetrimonium	83-113	albumin	Homo sapiens	158-171
29436987-4	2018	METHODS: Interaction of the anionic Sodium Dodecyl Sulphate (SDS) and the Cationic Cetyltrimethylammonium Bromide (CTAB) surfactants with domain III of Human Serum Albumin (HSA) has been studied using 8-Anilino-1-Naphthalene-Sulphonate (ANS) as a fluorescent marker.	Cetrimonium	115-119	albumin	Homo sapiens	158-171
28622544-5	2017	In this present work, we have studied the interaction of kappa-casein with cetyltrimethyl ammonium bromide (CTAB), a positively charged surfactant, utilizing various steady state fluorescence, time-resolved fluorescence and circular dichroism spectroscopy.	Cetrimonium	108-112	casein kappa	Homo sapiens	57-69
28622544-6	2017	Our results clearly indicate that kappa-casein undergoes at least two conformational transitions in presence of various concentrations of CTAB.	Cetrimonium	138-142	casein kappa	Homo sapiens	34-46
28622544-7	2017	The intrinsically disordered kappa-casein assumes a partially folded conformation at lower concentration of CTAB, which adopts an unstructured conformation at higher concentration of CTAB.	Cetrimonium	108-112	casein kappa	Homo sapiens	29-41
28622544-7	2017	The intrinsically disordered kappa-casein assumes a partially folded conformation at lower concentration of CTAB, which adopts an unstructured conformation at higher concentration of CTAB.	Cetrimonium	183-187	casein kappa	Homo sapiens	29-41
28622544-8	2017	The partially folded conformation of kappa-casein at a lower CTAB concentration might be induced by the favorable electrostatic interaction between the positively charged surfactant headgroup and net negative charges of the protein, whereas surfactant nature of CTAB is being pronounced at higher concentration of CTAB.	Cetrimonium	61-65	casein kappa	Homo sapiens	37-49
28622544-8	2017	The partially folded conformation of kappa-casein at a lower CTAB concentration might be induced by the favorable electrostatic interaction between the positively charged surfactant headgroup and net negative charges of the protein, whereas surfactant nature of CTAB is being pronounced at higher concentration of CTAB.	Cetrimonium	262-266	casein kappa	Homo sapiens	37-49
28622544-8	2017	The partially folded conformation of kappa-casein at a lower CTAB concentration might be induced by the favorable electrostatic interaction between the positively charged surfactant headgroup and net negative charges of the protein, whereas surfactant nature of CTAB is being pronounced at higher concentration of CTAB.	Cetrimonium	262-266	casein kappa	Homo sapiens	37-49
28831629-1	2017	Fluorescence properties of N, N"-bis(salicylidene) trans 1, 2-diaminocyclohexane (H 2 L) is used to probe the anionic (SDS), cationic (CTAB) and nonionic (TX-100) micelles as well as in serum albumins (BSA and HSA) and chicken egg white lysozyme (LYZ) by steady state and picosecond time-resolved fluorescence spectroscopy.	Cetrimonium	135-139	lysozyme (renal amyloidosis)	Gallus gallus	227-245
28831629-1	2017	Fluorescence properties of N, N"-bis(salicylidene) trans 1, 2-diaminocyclohexane (H 2 L) is used to probe the anionic (SDS), cationic (CTAB) and nonionic (TX-100) micelles as well as in serum albumins (BSA and HSA) and chicken egg white lysozyme (LYZ) by steady state and picosecond time-resolved fluorescence spectroscopy.	Cetrimonium	135-139	lysozyme (renal amyloidosis)	Gallus gallus	247-250
28235720-1	2017	Sandwich-like molybdenum sulfide/mesoporous organosilica nanosheets (denoted as MoS2@MOS) have been prepared for the first time via direct growth of ethane-bridged mesostructured organosilica on MoS2 nanosheets by using cetyltrimethylammonium bromide (CTAB) as structure directing agent.	Cetrimonium	220-250	MOS proto-oncogene, serine/threonine kinase	Homo sapiens	85-88
28933729-5	2017	The association of the Fe(III)MP-11 with CTAB and Cu(II)MP-11 with DODAB affected the colloidal stability of the surfactants that was recovered by heating.	Cetrimonium	41-45	non-compact myelin associated protein	Homo sapiens	30-35
28235720-1	2017	Sandwich-like molybdenum sulfide/mesoporous organosilica nanosheets (denoted as MoS2@MOS) have been prepared for the first time via direct growth of ethane-bridged mesostructured organosilica on MoS2 nanosheets by using cetyltrimethylammonium bromide (CTAB) as structure directing agent.	Cetrimonium	252-256	MOS proto-oncogene, serine/threonine kinase	Homo sapiens	85-88
28391869-5	2017	Curcumin along with CTAB act as capping and stabilizing agent for Au NWs/NPs in different temperatures, which is confirmed by XRD, TGA, DSC, EDX and FT-IR data.	Cetrimonium	20-24	T-box transcription factor 1	Homo sapiens	131-134
28391869-5	2017	Curcumin along with CTAB act as capping and stabilizing agent for Au NWs/NPs in different temperatures, which is confirmed by XRD, TGA, DSC, EDX and FT-IR data.	Cetrimonium	20-24	desmocollin 3	Homo sapiens	136-139
28277034-3	2017	For CTAB micelles, all fibers were able to enter the micelles, but the hair-like structure and chemical surface characteristics of GF1 modified the micelle structure toward a bilayer-like organization, while MD8 and BV12, being shorter fibers and with a high density of surface interacting groups, partially destroyed the micelles.	Cetrimonium	4-8	GATA binding protein 1	Homo sapiens	131-134
28333050-7	2017	The rate enhancement effect for CTAB might be due to micellar surface catalysis, through the Coulomb attraction between the reactants and positively charged surfactants, while the catalytic action for HA resulted from the additional oxidation of Fe(V)/Fe(IV) in the presence of HA.	Cetrimonium	32-36	FEV transcription factor, ETS family member	Homo sapiens	246-251
28134362-5	2017	XRD, TGA, DSC, EDX, FT-IR and fluorescence spectroscopic analysis confirm that both CTAB and curcumin act as capping and stabilizing agents for Au NWs as well as Au NPs - there is no remarkable difference in the curcumin/CTAB content between Au NWs and NPs prepared in different pH environments.	Cetrimonium	84-88	T-box transcription factor 1	Homo sapiens	5-8
28134362-5	2017	XRD, TGA, DSC, EDX, FT-IR and fluorescence spectroscopic analysis confirm that both CTAB and curcumin act as capping and stabilizing agents for Au NWs as well as Au NPs - there is no remarkable difference in the curcumin/CTAB content between Au NWs and NPs prepared in different pH environments.	Cetrimonium	84-88	desmocollin 3	Homo sapiens	10-13
28124754-5	2017	As for acceptors, cetyltrimethylammonium bromide (CTAB)-capped GNRs were treated with 11-mercaptoundecanoic acid (MUDA) and then conjugated with Anti-PSA 2 (Ab2).	Cetrimonium	18-48	kallikrein related peptidase 3	Homo sapiens	150-153
28124754-5	2017	As for acceptors, cetyltrimethylammonium bromide (CTAB)-capped GNRs were treated with 11-mercaptoundecanoic acid (MUDA) and then conjugated with Anti-PSA 2 (Ab2).	Cetrimonium	50-54	kallikrein related peptidase 3	Homo sapiens	150-153
28193331-2	2017	The CTAB capped gold nanoshells are electrostatically attracted by both the bacterial surface and the enzyme beta-galactosidase.	Cetrimonium	4-8	galactosidase beta 1	Homo sapiens	109-127
28193331-3	2017	The preferential binding of cationic (CTAB)-functionalized gold nanoshells to the more negative bacterial surfaces leaves active beta-galactosidase in solution, providing an enzyme-amplified colorimetric response of the binding event.	Cetrimonium	38-42	galactosidase beta 1	Homo sapiens	129-147
27642068-3	2016	Within an unexpectedly polar active site, CutC orients choline through hydrogen bonding with a putative general base, and through close interactions between phenolic and carboxylate oxygen atoms of the protein scaffold and the polarized methyl groups of the trimethylammonium moiety.	Cetrimonium	258-275	cutC copper transporter	Homo sapiens	42-46
27651074-2	2016	UCP was firstly transferred to aqueous phase using cationic surfactant cetyl trimethyl ammonium bromide (CTAB) via hydrophobic interaction without removing the existing oleic acid (OA).	Cetrimonium	71-103	uncoupling protein 1	Homo sapiens	0-3
27651074-2	2016	UCP was firstly transferred to aqueous phase using cationic surfactant cetyl trimethyl ammonium bromide (CTAB) via hydrophobic interaction without removing the existing oleic acid (OA).	Cetrimonium	105-109	uncoupling protein 1	Homo sapiens	0-3
28330193-5	2016	Here, we used an improved Sodium dodecyl sulfate-Cetyltrimethyl ammonium bromide-Chloroform-isoamyl alcohol method by combining Sodium dodecyl sulfate with cetyl methylammonium bromide without addition of proteinase K, RNase K, and beta-mercaptoethanol.	Cetrimonium	49-80	ribonuclease K	Homo sapiens	219-226
27118152-2	2016	In this work, we have shown that the particle size, fiber density, surface area and pore volume of KCC-1 can be effectively controlled and tuned by changing various reaction parameters, such as the concentrations of urea, CTAB, 1-pentanol, reaction time, temperature, solvent ratio, and even outside stirring time.	Cetrimonium	222-226	solute carrier family 12 member 4	Homo sapiens	99-104
25483919-0	2015	CTAB micelles assisted rGO-AgNP hybrids for SERS detection of polycyclic aromatic hydrocarbons.	Cetrimonium	0-4	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	44-48
26660433-2	2016	BBOX contains an aromatic cage for the recognition of the positively charged trimethylammonium group of the gammaBB substrate.	Cetrimonium	77-94	gamma-butyrobetaine hydroxylase 1	Homo sapiens	0-4
26660433-3	2016	Enzyme binding and kinetic analyses on substrate analogues with P and As substituting for N in the trimethylammonium group show that the analogues are good BBOX substrates, which follow the efficiency trend N(+) >P(+) >As(+).	Cetrimonium	99-116	gamma-butyrobetaine hydroxylase 1	Homo sapiens	156-160
25988296-0	2015	Human serum albumin-mimetic chromatography based hexadecyltrimethylammonium bromide as a novel direct probe for protein binding of acidic drugs.	Cetrimonium	49-83	albumin	Homo sapiens	6-19
25944532-8	2015	Among all Gram-negative bacteria, 94.55% (n=52) of qacEDelta1-positive strains showed higher MICs (512 mg l(-1)) to CTAB.	Cetrimonium	116-120	QacEdelta1	Escherichia coli	51-61
25483919-1	2015	A structure of hexadecyl trimethyl ammonium bromide (CTAB) micelle-assisted reduced graphene oxide-Ag nanoparticle (rGO-AgNP) hybrids is designed and fabricated for SERS detection of nonpolar polycyclic aromatic hydrocarbons (PAHs), in which CTAB micelles act as the host material to capture PAH molecules.	Cetrimonium	15-51	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	165-169
25483919-1	2015	A structure of hexadecyl trimethyl ammonium bromide (CTAB) micelle-assisted reduced graphene oxide-Ag nanoparticle (rGO-AgNP) hybrids is designed and fabricated for SERS detection of nonpolar polycyclic aromatic hydrocarbons (PAHs), in which CTAB micelles act as the host material to capture PAH molecules.	Cetrimonium	53-57	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	165-169
25483919-1	2015	A structure of hexadecyl trimethyl ammonium bromide (CTAB) micelle-assisted reduced graphene oxide-Ag nanoparticle (rGO-AgNP) hybrids is designed and fabricated for SERS detection of nonpolar polycyclic aromatic hydrocarbons (PAHs), in which CTAB micelles act as the host material to capture PAH molecules.	Cetrimonium	242-246	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	165-169
25483919-3	2015	The result shows that the CTAB-assisted rGO-AgNP substrate has excellent SERS performance toward PAHs and ideal stability under continuous laser radiation.	Cetrimonium	26-30	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	73-77
29403936-1	2015	A multi-walled carbon nanotube (MWCNT)-cetyltrimethylammonium bromide (CTAB) surfactant composite modified glassy carbon electrode (GCE) was developed as a novel system for the determination of 4-aminoantipyrine(AAP).	Cetrimonium	39-69	serpin family F member 2	Homo sapiens	212-215
29403936-1	2015	A multi-walled carbon nanotube (MWCNT)-cetyltrimethylammonium bromide (CTAB) surfactant composite modified glassy carbon electrode (GCE) was developed as a novel system for the determination of 4-aminoantipyrine(AAP).	Cetrimonium	71-75	serpin family F member 2	Homo sapiens	212-215
29403936-6	2015	The present electrochemical sensor based on the MWCNT-CTAB/GCE electrode was applied to the determination of AAP in real samples.	Cetrimonium	54-58	serpin family F member 2	Homo sapiens	109-112
25956050-4	2015	The obtained nanoparticles, denoted as PTX/TET-CTAB@MSN, exhibited pH-responsive release property with more easily released in the weak acidic environment.	Cetrimonium	47-51	moesin	Homo sapiens	52-55
25956050-6	2015	Furthermore, the PTX/TET-CTAB@MSN suppressed tumor cells growth more efficiently than only delivery of PTX (PTX-CTAB@MSN) or the free PTX.	Cetrimonium	25-29	moesin	Homo sapiens	30-33
25956050-6	2015	Furthermore, the PTX/TET-CTAB@MSN suppressed tumor cells growth more efficiently than only delivery of PTX (PTX-CTAB@MSN) or the free PTX.	Cetrimonium	25-29	moesin	Homo sapiens	108-120
26016687-1	2015	In this study, a facile one-pot process for the synthesis of hierarchical VS2/graphene nanosheets (VS2/GNS) composites based on the coincident interaction of VS2 and reduced graphene oxide (rGO) sheets in the presence of cetyltrimethylammonium bromide is developed for the first time.	Cetrimonium	221-251	glucosamine (N-acetyl)-6-sulfatase	Homo sapiens	99-106
25682837-3	2015	Herein, we employ fluorescence correlation spectroscopy (FCS) to track the structural transition of bovine serum albumin (BSA) in low concentrated cationic (cetyltrimethylammonium chloride, CTAC), anionic (sodium dodecyl sulfate, SDS), and nonionic (pentaethylene glycol monododecyl ether, C12E5 and octaethylene glycol monododecyl ether, C12E8) surfactant solutions.	Cetrimonium	190-194	albumin	Homo sapiens	107-120
25909588-2	2015	The positively charged GNRs and GNPs due to the surface immobilized cetyltrimethyl ammonium bromide (CTAB) can adsorb the negatively charged AFP antibody (Ab) directly.	Cetrimonium	68-99	alpha fetoprotein	Homo sapiens	141-144
25909588-2	2015	The positively charged GNRs and GNPs due to the surface immobilized cetyltrimethyl ammonium bromide (CTAB) can adsorb the negatively charged AFP antibody (Ab) directly.	Cetrimonium	101-105	alpha fetoprotein	Homo sapiens	141-144
26301093-5	2015	CTAB-coated Au NRs induce remarkable levels of autophagy activity as evidenced by LC3-II conversion and p62 degradation, while PSS- and PDDAC-coated Au NRs barely induce autophagy.	Cetrimonium	0-4	nucleoporin 62	Homo sapiens	104-107
26301093-6	2015	More importantly, we also demonstrated that the AKT-mTOR signaling pathway was responsible for CTAB-coated Au NRs-induced autophagy.	Cetrimonium	95-99	AKT serine/threonine kinase 1	Homo sapiens	48-51
26301093-6	2015	More importantly, we also demonstrated that the AKT-mTOR signaling pathway was responsible for CTAB-coated Au NRs-induced autophagy.	Cetrimonium	95-99	mechanistic target of rapamycin kinase	Homo sapiens	52-56
25706195-1	2015	In this work, we investigate the ligand exchange of cetyltrimethylammonium bromide (CTAB) with bovine serum albumin for gold nanorods.	Cetrimonium	52-82	albumin	Homo sapiens	102-115
25706195-1	2015	In this work, we investigate the ligand exchange of cetyltrimethylammonium bromide (CTAB) with bovine serum albumin for gold nanorods.	Cetrimonium	84-88	albumin	Homo sapiens	102-115
25460715-0	2015	Modification of an Iranian clinoptilolite nano-particles by hexadecyltrimethyl ammonium cationic surfactant and dithizone for removal of Pb(II) from aqueous solution.	Cetrimonium	60-87	submaxillary gland androgen regulated protein 3B	Homo sapiens	137-143
25460715-2	2015	The MCP and NCP powders were respectively modified with hexadecyltrimethyl ammonium bromide (HDTMA) and dithizone (DTZ).	Cetrimonium	56-91	CD46 molecule	Homo sapiens	4-7
25460715-2	2015	The MCP and NCP powders were respectively modified with hexadecyltrimethyl ammonium bromide (HDTMA) and dithizone (DTZ).	Cetrimonium	93-98	CD46 molecule	Homo sapiens	4-7
25016644-5	2014	Finally, we exploited a convenient approach for preparing water-soluble GNRs with less toxicity, better dispersion and flexible functionalization by exchanging hexadecyltrimethylammonium bromide (CTAB) on the surface of the rods with carboxylated bovine serum albumin (BSA) derivative, the BSA modified GNRs showed significant anticancer efficacy through near infrared (NIR) hyperthermia.	Cetrimonium	160-194	albumin	Homo sapiens	254-267
25010336-4	2014	Interestingly, it was found that the CTAB bilayer confined at the interface of carbon dots can amplify H2O2 induced ultraweak CL emissions, such as the Co(II)-triggered Fenton-like reaction, the peroxynitrous acid (ONOOH) system, and the peroxymonocarbonate (HCO4(-)) system.	Cetrimonium	37-41	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	152-157
25016644-5	2014	Finally, we exploited a convenient approach for preparing water-soluble GNRs with less toxicity, better dispersion and flexible functionalization by exchanging hexadecyltrimethylammonium bromide (CTAB) on the surface of the rods with carboxylated bovine serum albumin (BSA) derivative, the BSA modified GNRs showed significant anticancer efficacy through near infrared (NIR) hyperthermia.	Cetrimonium	196-200	albumin	Homo sapiens	254-267
24607128-1	2014	A new separation system of capillary electrophoresis (CE1) for the highly sensitive determination of copper was established by using ethylenediaminetetraacetic acid (EDTA) as a complexing agent and employing cetyltrimethylammonium chloride (CTAC) as a capillary inner wall modifier.	Cetrimonium	208-239	carboxylesterase 1	Homo sapiens	54-57
24607128-1	2014	A new separation system of capillary electrophoresis (CE1) for the highly sensitive determination of copper was established by using ethylenediaminetetraacetic acid (EDTA) as a complexing agent and employing cetyltrimethylammonium chloride (CTAC) as a capillary inner wall modifier.	Cetrimonium	241-245	carboxylesterase 1	Homo sapiens	54-57
24029460-2	2013	It is evident that bentonite modified with hexadecyl trimethyl ammonium (DK1) can effectively remove amoxicillin from aqueous solution.	Cetrimonium	43-71	immunoglobulin heavy diversity 5-12	Homo sapiens	73-76
24128586-2	2014	The amplifications of lectin gene, used to check the presence of soybean DNA, were not achieved in all CTAB extracts of DNA, while commercial kit gave satisfactory results.	Cetrimonium	103-107	LOW QUALITY PROTEIN: lectin	Glycine max	22-28
23845496-2	2013	The selective addition of sulfite to the alkene of TSP assisted by cetyltrimethyl ammonium bromide (CTAB) micelle can be visualized by dramatic color and ratiometric fluorescence changes.	Cetrimonium	67-98	thrombospondin 1	Homo sapiens	51-54
23875531-1	2013	The effect of ionic surfactants, sodium dodecyl sulfate (SDS) and N-cetyl-N,N,N-trimethylammonium bromide (CTAB), on the interaction between beta-agonist salbutamol (SAL) and bovine serum albumin (BSA) was investigated with the use of fluorescence spectroscopy (FLS) and chemometrics methods [multivariate curve resolution-alternating least-squares (MCR-ALS) and parallel factor analysis algorithm (PARAFAC)].	Cetrimonium	66-105	albumin	Homo sapiens	182-195
25490843-3	2013	The studied 20 aklaloid diesters and 10 trimethylammonium derivatives turned out to be non-competitive reversible inhibitors of acetylcholinesterase and competitive inhibitors of butyrylcholinesterase.	Cetrimonium	40-57	acetylcholinesterase (Cartwright blood group)	Homo sapiens	128-148
23845496-2	2013	The selective addition of sulfite to the alkene of TSP assisted by cetyltrimethyl ammonium bromide (CTAB) micelle can be visualized by dramatic color and ratiometric fluorescence changes.	Cetrimonium	100-104	thrombospondin 1	Homo sapiens	51-54
23845496-3	2013	In CTAB-PBS system, the fluorescence intensity ratio at 465 nm and 592 nm (I465/I592) and the absorbance ratio at 390 nm and 470 nm (A390/A470) were linearly proportional to sulfite concentration in the range of 0.5-150 muM, and the detection limit was 0.2 muM.	Cetrimonium	3-7	latexin	Homo sapiens	220-223
23845496-3	2013	In CTAB-PBS system, the fluorescence intensity ratio at 465 nm and 592 nm (I465/I592) and the absorbance ratio at 390 nm and 470 nm (A390/A470) were linearly proportional to sulfite concentration in the range of 0.5-150 muM, and the detection limit was 0.2 muM.	Cetrimonium	3-7	latexin	Homo sapiens	257-260
23377825-0	2013	Identification of cetrimonium bromide and irinotecan as compounds with synthetic lethality against NDRG1 deficient prostate cancer cells.	Cetrimonium	18-37	N-myc downstream regulated 1	Homo sapiens	99-104
23377825-6	2013	Screening of 3360 compounds revealed irinotecan and cetrimonium bromide (CTAB) as compounds that exhibited synthetic lethality against NDRG1 deficient PCa cells.	Cetrimonium	52-71	N-myc downstream regulated 1	Homo sapiens	135-140
23377825-6	2013	Screening of 3360 compounds revealed irinotecan and cetrimonium bromide (CTAB) as compounds that exhibited synthetic lethality against NDRG1 deficient PCa cells.	Cetrimonium	73-77	N-myc downstream regulated 1	Homo sapiens	135-140
23377825-9	2013	Our results suggest that CTAB and irinotecan could be further explored for their potential clinical benefit in patients with NDRG1 deficient PCa.	Cetrimonium	25-29	N-myc downstream regulated 1	Homo sapiens	125-130
23389781-5	2013	Compounds effective on AChE carry the 2-dimethylaminoethyl moiety, which resembles the trimethylammonium group and the ethylene bridge of acetylcholine.	Cetrimonium	87-104	acetylcholinesterase (Cartwright blood group)	Homo sapiens	23-27
23419511-2	2013	A selective separation of formate was achieved in approximately 1 min using an electrolyte system comprising 10 mM L-histidine, 15 mM glutamic acid and 30 muM cetyltrimethylammonium bromide at pH 4.56.	Cetrimonium	159-189	latexin	Homo sapiens	155-158
23507756-2	2013	The rapid and room temperature synthesis of magnetic nanoparticles was achieved using the hydroxylamine reduction of HAuCl4 on the surface of ethylenediaminetetraacetic acid (EDTA)-immobilized iron (magnetite Fe3O4) nanoparticles in the presence of an aqueous solution of hexadecyltrimetylammonium bromide (CTAB) as a dispersant.	Cetrimonium	307-311	outer membrane receptor FepA	Escherichia coli	193-197
23166012-8	2013	Both SOD and CAT activities showed similar associations with varied concentrations of surfactants: SOD was significantly promoted by 550 to 1,800 mg/L SDBS, 0.7 to 1.3 mg/L CTAC, and mixtures at levels 2 to 4; CAT was clearly promoted by 900 mg/L SDBS, 0.4 to 1.3 mg/L CTAC, and mixtures at levels 2 to 4.	Cetrimonium	173-177	catalase	Canis lupus familiaris	13-16
23166012-8	2013	Both SOD and CAT activities showed similar associations with varied concentrations of surfactants: SOD was significantly promoted by 550 to 1,800 mg/L SDBS, 0.7 to 1.3 mg/L CTAC, and mixtures at levels 2 to 4; CAT was clearly promoted by 900 mg/L SDBS, 0.4 to 1.3 mg/L CTAC, and mixtures at levels 2 to 4.	Cetrimonium	269-273	catalase	Canis lupus familiaris	13-16
23166012-8	2013	Both SOD and CAT activities showed similar associations with varied concentrations of surfactants: SOD was significantly promoted by 550 to 1,800 mg/L SDBS, 0.7 to 1.3 mg/L CTAC, and mixtures at levels 2 to 4; CAT was clearly promoted by 900 mg/L SDBS, 0.4 to 1.3 mg/L CTAC, and mixtures at levels 2 to 4.	Cetrimonium	269-273	catalase	Canis lupus familiaris	210-213
22987585-1	2012	In this study, we extensively report the effect of glycine betaine during the refolding of partially folded bovine alpha-lactalbumin (alpha-LA) in presence of hexadecyl trimethyl ammonium bromide (HTAB), and Ribonuclease A (RNAse A) in presence of sodium dodecyl sulfate (SDS) by different complementary biophysical, light scattering, and microscopic techniques.	Cetrimonium	159-195	lactalbumin alpha	Bos taurus	115-132
23233428-3	2013	This was achieved by treating the metal complexes with MSNs that contained the templating surfactant molecules confined within the silica channels (hexadecyltrimethylammonium (CTA)/MSN), followed by extraction of the surfactant.	Cetrimonium	148-174	moesin	Homo sapiens	55-58
23964551-9	2013	The Cetavlon-precipitated mannans of fungi induced cytokine responses that were similar or superior to those induced by whole extracts, C albicans being the most potent inducer of IFN-gamma.	Cetrimonium	4-12	interferon gamma	Homo sapiens	180-189
23334913-3	2013	To this end, we have also studied the ET dynamics of RBP-Rf complex under the confinement of a cationic hexadecyltrimethylammonium bromide (CTAB) RMs with similar water pool size to the anionic AOT-RMs towards simulating equal restricted volume effect.	Cetrimonium	104-138	retinol binding protein 4	Homo sapiens	53-56
23334913-3	2013	To this end, we have also studied the ET dynamics of RBP-Rf complex under the confinement of a cationic hexadecyltrimethylammonium bromide (CTAB) RMs with similar water pool size to the anionic AOT-RMs towards simulating equal restricted volume effect.	Cetrimonium	140-144	retinol binding protein 4	Homo sapiens	53-56
23018861-1	2012	This work demonstrates a remarkable enhancement in the peroxidase activity of mitochondrial membrane protein cytochrome c (cyt c) by perturbing its tertiary structure in the presence of surface-functionalised gold nanoparticles (GNPs) within cetyltrimethylammonium bromide (CTAB) reverse micelles.	Cetrimonium	242-272	cytochrome c, somatic	Homo sapiens	109-121
23018861-1	2012	This work demonstrates a remarkable enhancement in the peroxidase activity of mitochondrial membrane protein cytochrome c (cyt c) by perturbing its tertiary structure in the presence of surface-functionalised gold nanoparticles (GNPs) within cetyltrimethylammonium bromide (CTAB) reverse micelles.	Cetrimonium	242-272	cytochrome c, somatic	Homo sapiens	123-128
23018861-1	2012	This work demonstrates a remarkable enhancement in the peroxidase activity of mitochondrial membrane protein cytochrome c (cyt c) by perturbing its tertiary structure in the presence of surface-functionalised gold nanoparticles (GNPs) within cetyltrimethylammonium bromide (CTAB) reverse micelles.	Cetrimonium	274-278	cytochrome c, somatic	Homo sapiens	109-121
23018861-1	2012	This work demonstrates a remarkable enhancement in the peroxidase activity of mitochondrial membrane protein cytochrome c (cyt c) by perturbing its tertiary structure in the presence of surface-functionalised gold nanoparticles (GNPs) within cetyltrimethylammonium bromide (CTAB) reverse micelles.	Cetrimonium	274-278	cytochrome c, somatic	Homo sapiens	123-128
23018861-3	2012	The surfactant shell of the CTAB reverse micelle in the presence of co-surfactant (n-hexanol) exerted higher crowding effects on the interfacially bound cyt c than similar anionic systems.	Cetrimonium	28-32	cytochrome c, somatic	Homo sapiens	153-158
22987585-1	2012	In this study, we extensively report the effect of glycine betaine during the refolding of partially folded bovine alpha-lactalbumin (alpha-LA) in presence of hexadecyl trimethyl ammonium bromide (HTAB), and Ribonuclease A (RNAse A) in presence of sodium dodecyl sulfate (SDS) by different complementary biophysical, light scattering, and microscopic techniques.	Cetrimonium	159-195	lactalbumin alpha	Bos taurus	134-142
22394160-1	2012	Genetically engineered elastin-like polypeptides (ELP) can be interfaced with cetyltrimethyl ammonium bromide (CTAB)-stabilized gold nanorods (GNRs) resulting in the formation of stable dispersions (nanoassemblies).	Cetrimonium	78-109	nuclear receptor subfamily 5 group A member 1	Homo sapiens	23-48
22394160-1	2012	Genetically engineered elastin-like polypeptides (ELP) can be interfaced with cetyltrimethyl ammonium bromide (CTAB)-stabilized gold nanorods (GNRs) resulting in the formation of stable dispersions (nanoassemblies).	Cetrimonium	78-109	nuclear receptor subfamily 5 group A member 1	Homo sapiens	50-53
22394160-1	2012	Genetically engineered elastin-like polypeptides (ELP) can be interfaced with cetyltrimethyl ammonium bromide (CTAB)-stabilized gold nanorods (GNRs) resulting in the formation of stable dispersions (nanoassemblies).	Cetrimonium	111-115	nuclear receptor subfamily 5 group A member 1	Homo sapiens	23-48
22394160-1	2012	Genetically engineered elastin-like polypeptides (ELP) can be interfaced with cetyltrimethyl ammonium bromide (CTAB)-stabilized gold nanorods (GNRs) resulting in the formation of stable dispersions (nanoassemblies).	Cetrimonium	111-115	nuclear receptor subfamily 5 group A member 1	Homo sapiens	50-53
22394160-4	2012	The presence of cetyltrimethyl ammonium bromide (CTAB), used to template the formation of gold nanorods, plays a significant role in the phase separation behavior, with high concentrations of the surfactant leading to dramatic enhancements in ELP transition temperature.	Cetrimonium	16-47	nuclear receptor subfamily 5 group A member 1	Homo sapiens	243-246
22394160-4	2012	The presence of cetyltrimethyl ammonium bromide (CTAB), used to template the formation of gold nanorods, plays a significant role in the phase separation behavior, with high concentrations of the surfactant leading to dramatic enhancements in ELP transition temperature.	Cetrimonium	49-53	nuclear receptor subfamily 5 group A member 1	Homo sapiens	243-246
22394160-7	2012	Further analysis of the kinetics of nanocomposite formation using a mathematical model indicated that CTAB largely influenced the early event of coacervation of ELP-GNR nanoassemblies leading to nanocomposites, but had minimal effect on nanocomposite maturation, which is a later-stage longer event.	Cetrimonium	102-106	nuclear receptor subfamily 5 group A member 1	Homo sapiens	161-164
22304398-7	2012	We demonstrate pan-analyte immobilization of sized CTAB-laden model proteins (protein G, ovalbumin, bovine serum albumin, beta-galactosidase, lactoferrin) on the EIG with initial capture efficiencies ranging from 21 to 100%.	Cetrimonium	51-55	albumin	Homo sapiens	107-120
22304398-7	2012	We demonstrate pan-analyte immobilization of sized CTAB-laden model proteins (protein G, ovalbumin, bovine serum albumin, beta-galactosidase, lactoferrin) on the EIG with initial capture efficiencies ranging from 21 to 100%.	Cetrimonium	51-55	galactosidase beta 1	Homo sapiens	122-140
22149108-4	2012	The cavitand is capable of binding trimethylammonium-tagged guests from an aqueous medium and can be deposited in 2 x 2 microarrays on the surface for characterization by SPR imaging techniques.	Cetrimonium	35-52	sepiapterin reductase	Homo sapiens	171-174
21616501-1	2011	CdS nanoparticles were precipitated by the reaction of cadmium acetate with sodium sulphide in the presence of cetyltrimethylammonium (CTA) and deposited on montmorillonite (MMT).	Cetrimonium	111-133	CDP-diacylglycerol synthase 1	Homo sapiens	0-3
22400212-2	2011	Oligomeric alkyl-ethylene oxide surfactant [(Polyoxyethylene (2) cetyl ether, structure is C16H33(OCH2CH2)nOH, n-2, hereafter known as B52) and ionic surfactant (cethyltrimethylammonium bromide (CTAB)) templating systems form mixed micelles that self-assemble into well-ordered hexagonal and bimodal mesostructures.	Cetrimonium	195-199	serine and arginine rich splicing factor 6	Homo sapiens	135-138
21794868-1	2011	In this study, core-shell magnetic mesoporous microspheres with C18-functionalized interior pore-walls were synthesized through coating Fe(3)O(4) microspheres with a mesoporous inorganic-organic hybrid layer with a n-octadecyltriethoxysilane (C18TES) and tetraethyl orthosilicate (TEOS) as the silica source and cetyltrimethylammonia bromide (CTAB) as a template.	Cetrimonium	343-347	Bardet-Biedl syndrome 9	Homo sapiens	64-67
21616501-1	2011	CdS nanoparticles were precipitated by the reaction of cadmium acetate with sodium sulphide in the presence of cetyltrimethylammonium (CTA) and deposited on montmorillonite (MMT).	Cetrimonium	135-138	CDP-diacylglycerol synthase 1	Homo sapiens	0-3
21616501-2	2011	The resulting CdS-MMT nanocomposite contained 6 wt.% of CdS and 30 wt.% of CTA.	Cetrimonium	75-78	CDP-diacylglycerol synthase 1	Homo sapiens	14-17
21576447-2	2011	Analysis of the susceptibilities of the sugE-containing strain (Escherichia coli KAM32/pSUGE28) and sugE-deficient E. cloacae (EcDeltasugE) showed that SugE confers resistance to cetyltrimethylammonium bromide, cetylpyridinium chloride, tetraphenylphosphonium, benzalkonium chloride, ethidium bromide, and sodium dodecyl sulfate.	Cetrimonium	179-209	quaternary ammonium compound-resistance protein SugE	Escherichia coli	40-44
21576447-2	2011	Analysis of the susceptibilities of the sugE-containing strain (Escherichia coli KAM32/pSUGE28) and sugE-deficient E. cloacae (EcDeltasugE) showed that SugE confers resistance to cetyltrimethylammonium bromide, cetylpyridinium chloride, tetraphenylphosphonium, benzalkonium chloride, ethidium bromide, and sodium dodecyl sulfate.	Cetrimonium	179-209	quaternary ammonium compound-resistance protein SugE	Escherichia coli	152-156
21417400-1	2011	In this work we have shown a comparative study of changes in physicochemical properties of an aqueous solution of a common cationic surfactant cetyltrimethylammonium bromide (CTAB) upon addition of two protic ionic liquids N,N-dimethylethanolammonium [corrected] hexanoate (DAH) and N,N-dimethylethanolammonium [corrected] formate (DAF).	Cetrimonium	143-173	CD55 molecule (Cromer blood group)	Homo sapiens	332-335
21503356-0	2011	A colorimetric assay method for Co2+ based on thioglycolic acid functionalized hexadecyl trimethyl ammonium bromide modified Au nanoparticles (NPs).	Cetrimonium	79-115	complement C2	Homo sapiens	32-35
21417400-1	2011	In this work we have shown a comparative study of changes in physicochemical properties of an aqueous solution of a common cationic surfactant cetyltrimethylammonium bromide (CTAB) upon addition of two protic ionic liquids N,N-dimethylethanolammonium [corrected] hexanoate (DAH) and N,N-dimethylethanolammonium [corrected] formate (DAF).	Cetrimonium	175-179	CD55 molecule (Cromer blood group)	Homo sapiens	332-335
21417400-4	2011	At higher concentrations of additives (DAF and DAH), the properties of aqueous CTAB solution change in an entirely different way.	Cetrimonium	79-83	CD55 molecule (Cromer blood group)	Homo sapiens	39-50
21851044-1	2011	The influence of cationic detergent cetyltrimethylammonium on the human blood cholinesterases activity (erythrocyte acetylcholinesterase and plasma butyrylcholinesterase) in reactions of hydrolysis of alpha-thionaphthylacetat and acetylthiocholine is studied.	Cetrimonium	36-58	acetylcholinesterase (Cartwright blood group)	Homo sapiens	116-136
21851044-4	2011	Kinetic constants in reaction of acetylcholinesterase inhibition by cetyltrimethylammonium defined by means of different substrates--alpha-thionaphthylacetat and acetylthiocholin.	Cetrimonium	68-90	acetylcholinesterase (Cartwright blood group)	Homo sapiens	33-53
20638070-1	2010	The kinetics of the aggregation of bovine serum albumin (BSA) in the presence of N-cetyl-N,N,N-trimethyl ammonium bromide (CTAB) was studied by monitoring turbidity as a function of time.	Cetrimonium	81-121	albumin	Homo sapiens	42-55
21044789-1	2011	The role of different types of interactions and their contribution in the stabilization of bovine alpha-lactalbumin (alpha-LA) molten globule in presence of cationic surfactant, hexadecyl trimethyl ammonium bromide (HTAB) and anionic surfactant, sodium dodecyl sulphate (SDS) have been examined using a combination of spectroscopic, light scattering and calorimetric techniques.	Cetrimonium	216-220	lactalbumin alpha	Bos taurus	117-125
21137404-0	2010	[Preliminary investigation on the formation mechanism of CCL4-water-cetyl trimethyl ammonium bromide (CTAB) gel].	Cetrimonium	68-100	C-C motif chemokine ligand 4	Homo sapiens	57-61
21137404-0	2010	[Preliminary investigation on the formation mechanism of CCL4-water-cetyl trimethyl ammonium bromide (CTAB) gel].	Cetrimonium	102-106	C-C motif chemokine ligand 4	Homo sapiens	57-61
21137404-9	2010	So the authors suppose that CTAB is a synergistically solubilized by water and CCl4 in the gel.	Cetrimonium	28-32	C-C motif chemokine ligand 4	Homo sapiens	79-83
20599205-2	2010	Here we report the successful preparation of shell-like nano HAp spheres with fine morphology, uniform size around 200 nm, and stoichiometry ratio 1.7 with 56% nano- (<5 nm) and 44% mesoporosity using the surfactant tetradecyltrimethylammonium bromide (Cetrimide), which was not reported earlier.	Cetrimonium	256-265	reticulon 3	Homo sapiens	61-64
21237563-7	2011	In addition, after simply treated with CTAB, P(A-O)/AT nano-adsorbent showed better adsorption properties for phenol than the same kinds of materials.	Cetrimonium	39-43	polyamine oxidase	Homo sapiens	45-50
20638070-1	2010	The kinetics of the aggregation of bovine serum albumin (BSA) in the presence of N-cetyl-N,N,N-trimethyl ammonium bromide (CTAB) was studied by monitoring turbidity as a function of time.	Cetrimonium	123-127	albumin	Homo sapiens	42-55
20036372-6	2010	The decrease in eta(0) was due to the formation of branched wormlike micelles above once a concentration [CTAB]=20 mM.	Cetrimonium	106-110	endothelin receptor type A	Homo sapiens	16-19
20623177-1	2010	Hydroxyapatite (HAp) [Ca(10)(PO(4))(6)(OH)(2)] nanorods were synthesized using a surfactant templating method, with cetyltrimethylammonium bromide (CTAB) micelles acting as template for HAp growth.	Cetrimonium	116-146	reticulon 3	Homo sapiens	16-19
20623177-1	2010	Hydroxyapatite (HAp) [Ca(10)(PO(4))(6)(OH)(2)] nanorods were synthesized using a surfactant templating method, with cetyltrimethylammonium bromide (CTAB) micelles acting as template for HAp growth.	Cetrimonium	148-152	reticulon 3	Homo sapiens	16-19
21124625-3	2010	CTAB-modified silica nanoparticles were well dispersed in the polyamide-imide matrix, and the amount of silica nanoparticles to PAI was investigated to be from 2 to 10 wt%.	Cetrimonium	0-4	serpin family E member 1	Homo sapiens	128-131
20143862-9	2010	In concurrence with the observed highest activity in the presence of IL 2, the circular dichroism (CD) spectrum of trypsin in CTAB reverse micelles doped with IL 2 exhibited the lowest mean residue ellipticity (MRE), which is closest to that of the native protein in aqueous buffer.	Cetrimonium	126-130	interleukin 2	Homo sapiens	159-163
20056228-0	2010	Characterization of different conformations of bovine serum albumin and their propensity to aggregate in the presence of N-cetyl-N,N,N-trimethyl ammonium bromide.	Cetrimonium	121-161	albumin	Homo sapiens	54-67
20056228-1	2010	To characterize the structural changes in bovine serum albumin (BSA) on the addition of N-cetyl-N,N,N-trimethyl ammonium bromide (CTAB) and to understand the mechanism underlying aggregation of resulting protein-surfactant complex, UV-visible absorbance, steady-state fluorescence, SDS-PAGE gel electrophoresis, dynamic light scattering (DLS), and circular dichroism measurements of BSA-CTAB solutions were carried out.	Cetrimonium	88-128	albumin	Homo sapiens	49-62
20056228-1	2010	To characterize the structural changes in bovine serum albumin (BSA) on the addition of N-cetyl-N,N,N-trimethyl ammonium bromide (CTAB) and to understand the mechanism underlying aggregation of resulting protein-surfactant complex, UV-visible absorbance, steady-state fluorescence, SDS-PAGE gel electrophoresis, dynamic light scattering (DLS), and circular dichroism measurements of BSA-CTAB solutions were carried out.	Cetrimonium	130-134	albumin	Homo sapiens	49-62
20056228-1	2010	To characterize the structural changes in bovine serum albumin (BSA) on the addition of N-cetyl-N,N,N-trimethyl ammonium bromide (CTAB) and to understand the mechanism underlying aggregation of resulting protein-surfactant complex, UV-visible absorbance, steady-state fluorescence, SDS-PAGE gel electrophoresis, dynamic light scattering (DLS), and circular dichroism measurements of BSA-CTAB solutions were carried out.	Cetrimonium	387-391	albumin	Homo sapiens	49-62
20672138-5	2009	TGA/DTA analyses of the precursor In(OH)(3) and the final product In(2)O(3) confirm the existence of CTAB molecules, and its content is about 6%.	Cetrimonium	101-105	T-box transcription factor 1	Homo sapiens	0-3
20088512-4	2010	Reaction of [(18)F]fluoride at 40 degrees C with the trimethylammonium precursor afforded 6-[(18)F]fluoronicotinic acid tetrafluorophenyl ester ([(18)F]F-Py-TFP) directly in 60-70% yield.	Cetrimonium	53-70	inhibitor of carbonic anhydrase pseudogene	Homo sapiens	157-160
20299767-3	2010	Contrary to conventional systems in which worm-like micelles are formed, the zero-shear viscosity of the micellar solution in the water/CGT-n/CTAB system with n=1.2 increases with the addition of cationic cosurfactant and once decreases after a maximum, then increases again and decreases after the second maximum.	Cetrimonium	142-146	UDP glycosyltransferase 8	Homo sapiens	136-139
19383571-1	2009	The electrochemical properties of catechin at single-walled carbon nanotubes (SWNTs)-cetylramethylammonium bromide (CTAB) modified glassy carbon electrodes (GCE) were investigated by cyclic voltammetry (CV) and differential pulse voltammetry (DPV).	Cetrimonium	116-120	aminomethyltransferase	Homo sapiens	157-160
19154126-0	2009	Encapsulation of myoglobin in a cetyl trimethylammonium bromide micelle in vacuo: a simulation study.	Cetrimonium	32-63	myoglobin	Homo sapiens	17-26
19154126-8	2009	Myoglobin associates with CTAB surfactants in solution, but no complete reverse micelle is formed.	Cetrimonium	26-30	myoglobin	Homo sapiens	0-9
19428710-3	2009	Here, guanidinium hydrochloride-denatured hexameric leucine aminopeptidase is shown to be efficiently refolded by using the cationic detergent cetyltrimethylammonium bromide and the linear polysaccharide dextrin-10 as artificial chaperones.	Cetrimonium	143-173	carboxypeptidase Q	Homo sapiens	60-74
19118987-1	2009	The interaction of the cationic surfactant cetyltrimethylammonium bromide (CTAB) with bovine serum albumin (BSA), a globular protein, has been studied by small-angle neutron scattering (SANS), fluorescence and circular dichroism (CD).	Cetrimonium	43-73	albumin	Homo sapiens	93-106
19118987-1	2009	The interaction of the cationic surfactant cetyltrimethylammonium bromide (CTAB) with bovine serum albumin (BSA), a globular protein, has been studied by small-angle neutron scattering (SANS), fluorescence and circular dichroism (CD).	Cetrimonium	75-79	albumin	Homo sapiens	93-106
19154126-1	2009	A recently published paper describes encapsulation of myoglobin into cetyl trimethylammonium bromide (CTAB) micelles by electrospray ionization followed by detection using mass spectrometry [Sharon, M., et al.	Cetrimonium	69-100	myoglobin	Homo sapiens	54-63
19154126-1	2009	A recently published paper describes encapsulation of myoglobin into cetyl trimethylammonium bromide (CTAB) micelles by electrospray ionization followed by detection using mass spectrometry [Sharon, M., et al.	Cetrimonium	102-106	myoglobin	Homo sapiens	54-63
18458367-2	2008	In the present work, a novel sonochemical technique using CaHPO(4)2H(2)O/NaOH/distilled water with cetyltrimethylammonium bromide ((CH(3)(CH(2))(15)N(+)(CH(3))(3)Br(-)) designated as CTAB) under a hydrothermal condition to synthesize HAp nanostructure was described.	Cetrimonium	99-129	reticulon 3	Homo sapiens	234-237
19036430-3	2009	OVA and poly(I:C) were each ion-paired to cetyltrimethylammonium bromide (CTAB) to produce hydrophobic complexes, which were co-encapsulated in pH-sensitive polyketal (PK3) microparticles (1-3 microm) using a single emulsion method.	Cetrimonium	74-78	pyruvate kinase, muscle	Mus musculus	168-171
18853207-4	2009	The intracellular levels of ADH and G6PDH after permeabilization of these stored cells with cetyltrimetylammonium bromide (CTAB) were much higher, which showed only slight decrease within 2 weeks during the industrial storage.	Cetrimonium	123-127	glucose-6-phosphate dehydrogenase	Saccharomyces cerevisiae S288C	36-41
19161405-7	2009	The singlet-oxygen quenching constant for (GRP)(2)-canthaxanthin in micelles depends strongly on the specific detergent used, varying from 9.4 x 10(8) m(-1)s(-1) for hexadecyltrimethylammonium bromide (CTAB) to 1.24 +/- 0.4 x 10(10) m(-1)s(-1) for sodium dodecyl sulfate.	Cetrimonium	166-200	gastrin releasing peptide	Homo sapiens	43-46
19161405-7	2009	The singlet-oxygen quenching constant for (GRP)(2)-canthaxanthin in micelles depends strongly on the specific detergent used, varying from 9.4 x 10(8) m(-1)s(-1) for hexadecyltrimethylammonium bromide (CTAB) to 1.24 +/- 0.4 x 10(10) m(-1)s(-1) for sodium dodecyl sulfate.	Cetrimonium	202-206	gastrin releasing peptide	Homo sapiens	43-46
19161405-8	2009	The small quenching constant in CTAB micelles correlates with spectroscopic evidence for aggregation of the (GRP)(2)-canthaxanthin in this detergent.	Cetrimonium	32-36	gastrin releasing peptide	Homo sapiens	109-112
18656657-2	2008	Trace amounts of As(V) and Se(VI) species were separated and preconcentrated from total As and Se at desired pH values by a conical microcolumn packed with cetyltrimethylammonium bromide (CTAB)-modified alkyl silica sorbent in the absence of chelating reagent.	Cetrimonium	156-186	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	17-22
18656657-2	2008	Trace amounts of As(V) and Se(VI) species were separated and preconcentrated from total As and Se at desired pH values by a conical microcolumn packed with cetyltrimethylammonium bromide (CTAB)-modified alkyl silica sorbent in the absence of chelating reagent.	Cetrimonium	188-192	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	17-22
18371713-3	2008	Polyvinyl chloride (PVC)-based membranes of Cd-S(1) and Cd-S(2) using as hexadecyltrimethylammonium bromide (HTAB) cation discriminator and o-nitrophenyloctyl ether (o-NPOE), dibutylphthalate (DBP), acetophenone (AP) and tributylphosphate (TBP) as plasticizing solvent mediators were prepared and investigated as iodide-selective sensors.	Cetrimonium	109-113	CDP-diacylglycerol synthase 2	Homo sapiens	56-63
17845063-6	2007	The critical aggregate concentration is on the order of 10-4 g L-1 when the ionic blocks of PEO-PAMPS-PMAA are fully neutralized with CTAC.	Cetrimonium	134-138	immunoglobulin kappa variable 1-16	Homo sapiens	63-66
18838836-2	2008	Formation mechanism of the Hex-ncTiO(2)/CTAB Nanoskeleton was examined in terms of the reaction temperature, titania precursor/CTAB mixing ratio, surfactant type, electrostatic interaction, micelle formation and molecular component.	Cetrimonium	40-44	hematopoietically expressed homeobox	Homo sapiens	27-30
18838836-2	2008	Formation mechanism of the Hex-ncTiO(2)/CTAB Nanoskeleton was examined in terms of the reaction temperature, titania precursor/CTAB mixing ratio, surfactant type, electrostatic interaction, micelle formation and molecular component.	Cetrimonium	127-131	hematopoietically expressed homeobox	Homo sapiens	27-30
17471452-0	2007	A flow-injection chemiluminescence method for the determination of human serum albumin, using the reaction of fluorescein-human serum albumin-sodium hypochlorite by the enhancement effect of the cationic surfactant cetyltrimethylammonium bromide.	Cetrimonium	215-245	albumin	Homo sapiens	110-141
17471452-2	2007	It was found that the cationic surfactant cetyltrimethylammonium bromide (CTAB) could cause the structural transformation of fluorescein from the quinone to the spirolactone form, and greatly enhance the CL intensity of the fluorescein-human serum albumin (HSA) complex.	Cetrimonium	42-72	albumin	Homo sapiens	224-255
17471452-2	2007	It was found that the cationic surfactant cetyltrimethylammonium bromide (CTAB) could cause the structural transformation of fluorescein from the quinone to the spirolactone form, and greatly enhance the CL intensity of the fluorescein-human serum albumin (HSA) complex.	Cetrimonium	42-72	albumin	Homo sapiens	257-260
17471452-2	2007	It was found that the cationic surfactant cetyltrimethylammonium bromide (CTAB) could cause the structural transformation of fluorescein from the quinone to the spirolactone form, and greatly enhance the CL intensity of the fluorescein-human serum albumin (HSA) complex.	Cetrimonium	74-78	albumin	Homo sapiens	224-255
17471452-2	2007	It was found that the cationic surfactant cetyltrimethylammonium bromide (CTAB) could cause the structural transformation of fluorescein from the quinone to the spirolactone form, and greatly enhance the CL intensity of the fluorescein-human serum albumin (HSA) complex.	Cetrimonium	74-78	albumin	Homo sapiens	257-260
17043805-2	2007	The results showed that the activities of alcohol dehydrogenase (ADH) and glucose-6-phosphate dehydrogenase (G6PDH) in CTAB permeabilized brewer"s yeast cells increased 525 and 7.9-fold, respectively, compared with that in the nonpermeabilized cells and had high enantioselectivity to convert COBE to (R)-CHBE.	Cetrimonium	119-123	glucose-6-phosphate dehydrogenase	Saccharomyces cerevisiae S288C	74-107
17468053-2	2007	Cetyltrimethyl ammonium bromide (CTAB) was used to modify the surface of PBCA NPs, and then the plasmid DNA (pDNA) of pAFP-TK was wrapped into PBCA-CTAB NPs.	Cetrimonium	0-31	PBCA	Homo sapiens	73-77
17468053-2	2007	Cetyltrimethyl ammonium bromide (CTAB) was used to modify the surface of PBCA NPs, and then the plasmid DNA (pDNA) of pAFP-TK was wrapped into PBCA-CTAB NPs.	Cetrimonium	33-37	PBCA	Homo sapiens	73-77
17468053-2	2007	Cetyltrimethyl ammonium bromide (CTAB) was used to modify the surface of PBCA NPs, and then the plasmid DNA (pDNA) of pAFP-TK was wrapped into PBCA-CTAB NPs.	Cetrimonium	148-152	PBCA	Homo sapiens	143-147
17468053-3	2007	Atomic force microscopy and zeta potential demonstrated that PBCA-CTAB NPs were 80-200 nm in diameter and had +15.6 mV positive surface charges.	Cetrimonium	66-70	PBCA	Homo sapiens	61-65
17468053-4	2007	Assay using 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide showed that PBCA-CTAB NPs had less cytotoxicity to 3T3 cells than HepG2 cells.	Cetrimonium	94-98	PBCA	Homo sapiens	89-93
17468053-6	2007	Furthermore, when PBCA-CTAB NPs combined with suicide gene pAFP-TK, alpha-fetoprotein-positive cells transfected by it were highly sensitive to ganciclovir treatment, and cell survival declined precipitously.	Cetrimonium	23-27	PBCA	Homo sapiens	18-22
17468053-6	2007	Furthermore, when PBCA-CTAB NPs combined with suicide gene pAFP-TK, alpha-fetoprotein-positive cells transfected by it were highly sensitive to ganciclovir treatment, and cell survival declined precipitously.	Cetrimonium	23-27	alpha fetoprotein	Homo sapiens	68-85
17043805-2	2007	The results showed that the activities of alcohol dehydrogenase (ADH) and glucose-6-phosphate dehydrogenase (G6PDH) in CTAB permeabilized brewer"s yeast cells increased 525 and 7.9-fold, respectively, compared with that in the nonpermeabilized cells and had high enantioselectivity to convert COBE to (R)-CHBE.	Cetrimonium	119-123	glucose-6-phosphate dehydrogenase	Saccharomyces cerevisiae S288C	109-114
16738718-0	2006	Magnetic alignment of aqueous CTAB in nematic and hexagonal liquid crystalline phases investigated by spin-1 NMR.	Cetrimonium	30-34	spindlin 1	Homo sapiens	102-108
16765977-1	2006	In this study, the interaction of the anion of quinapril (QUIN), angiotensin converting enzyme (ACE) inhibitor, with cationic surfactant cetyltrimethylammonium bromide (CTAB) was investigated.	Cetrimonium	137-167	angiotensin I converting enzyme	Homo sapiens	65-94
16765977-1	2006	In this study, the interaction of the anion of quinapril (QUIN), angiotensin converting enzyme (ACE) inhibitor, with cationic surfactant cetyltrimethylammonium bromide (CTAB) was investigated.	Cetrimonium	137-167	angiotensin I converting enzyme	Homo sapiens	96-99
16765977-1	2006	In this study, the interaction of the anion of quinapril (QUIN), angiotensin converting enzyme (ACE) inhibitor, with cationic surfactant cetyltrimethylammonium bromide (CTAB) was investigated.	Cetrimonium	169-173	angiotensin I converting enzyme	Homo sapiens	65-94
16765977-1	2006	In this study, the interaction of the anion of quinapril (QUIN), angiotensin converting enzyme (ACE) inhibitor, with cationic surfactant cetyltrimethylammonium bromide (CTAB) was investigated.	Cetrimonium	169-173	angiotensin I converting enzyme	Homo sapiens	96-99
17209586-2	2007	Hexagonal, cubic, and lamellar lyotropic liquid crystalline phases were observed in PIL-hexadecyltrimethylammonium bromide systems.	Cetrimonium	88-122	serpin family A member 2 (gene/pseudogene)	Homo sapiens	84-87
17209632-4	2007	In contrast, a hydrogenated cationic surfactant with the same headgroup, hexadecyltrimethylammonium bromide, is shown to associate to lysozyme.	Cetrimonium	73-107	lysozyme	Homo sapiens	134-142
16822714-1	2007	A simple, highly sensitive assay for fibronectin (Fn) was reported using resonance light-scattering (RLS) technique based on the enhanced RLS intensity of hyperin-cetyltrimethylammonium bromide (CTMAB)-Fn system.	Cetrimonium	195-200	fibronectin 1	Homo sapiens	37-48
16738718-1	2006	Spin-1 NMR has been used to characterize the magnetically aligned nematic and hexagonal liquid crystalline phases of aqueous cetyltrimethylammonium bromide (CTAB).	Cetrimonium	125-155	spindlin 1	Homo sapiens	0-6
16738718-1	2006	Spin-1 NMR has been used to characterize the magnetically aligned nematic and hexagonal liquid crystalline phases of aqueous cetyltrimethylammonium bromide (CTAB).	Cetrimonium	157-161	spindlin 1	Homo sapiens	0-6
16245689-4	2005	AChE is shown to hydrolyze only those substrates that form equilibrium conformers compatible in the mutual arrangement of trimethylammonium group, carbonyl carbon, and carbonyl oxygen with the tt conformation of ACh; in this case, the rate of substrate hydrolysis depends on the total population of these conformers.	Cetrimonium	122-139	acetylcholinesterase (Cartwright blood group)	Homo sapiens	0-4
16633684-2	2006	In this work we have demonstrated that the association of Fe(III)MP-9 and Fe(III)MP-11 with CTAB micelles (MP-9/CTAB and MP11/CTAB) provides a microenvironment with an alkaline interface and a hydrophobic core that exhibits peroxidase behavior.	Cetrimonium	92-96	non-compact myelin associated protein	Homo sapiens	121-125
16386299-2	2005	CTAB monomer can convert methemoglobin (metHb) to hemichrome, and CTAB molecular assemblies, such as micelle, microemulsion and lamellar liquid crystal, can induce heme monomer to leave the hydrophobic cavity of Hb.	Cetrimonium	0-4	hemoglobin subunit gamma 2	Homo sapiens	25-38
16132338-3	2005	METHODS: The permeation-enhancing properties of the well-established permeation enhancers sodium deoxycholate (Na DOC) and cetrimide on the permeation of PACAP were investigated on freshly excised porcine buccal mucosa in Ussing chambers.	Cetrimonium	123-132	adenylate cyclase activating polypeptide 1	Homo sapiens	154-159
16394125-2	2005	Previously, we have shown that antisense oligonucleotides designed against EWS-Fli-1 inhibited tumor growth in nude mice provided they were delivered intratumorally by nanocapsules or by CTAB-coated nanospheres.	Cetrimonium	187-191	Ewing sarcoma breakpoint region 1	Mus musculus	75-78
16394125-2	2005	Previously, we have shown that antisense oligonucleotides designed against EWS-Fli-1 inhibited tumor growth in nude mice provided they were delivered intratumorally by nanocapsules or by CTAB-coated nanospheres.	Cetrimonium	187-191	Friend leukemia integration 1	Mus musculus	79-84
16830772-4	2006	The epsilon values of Al-CAS and Al-CAS-CTMAB were determined with water reference.	Cetrimonium	40-45	BCAR1 scaffold protein, Cas family member	Homo sapiens	36-39
18970495-5	2006	Diethyldithiocarbomate (DDC) in a cationic micellar solution of cetyltrimethylammonium bromide (CTAB) was used for determination of Fe(II), Co(II) and Cu(II) at pH 5.50.	Cetrimonium	96-100	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	140-146
16246394-0	2005	Removing low ppb level perchlorate, RDX, and HMX from groundwater with cetyltrimethylammonium chloride (CTAC) pre-loaded activated carbon.	Cetrimonium	71-102	radixin	Homo sapiens	36-39
16246394-7	2005	RDX was detected in the effluent from the CTAC-pre-loaded bed after only 8000 BV had been processed whereas 308,000 BV could be processed through the virgin bed before RDX was detected.	Cetrimonium	42-46	radixin	Homo sapiens	0-3
16246394-9	2005	However, by combining a CTAC-pre-loaded bed followed by a virgin GAC bed in series, both perchlorate and RDX could be removed for the same length of time.	Cetrimonium	24-28	radixin	Homo sapiens	105-108
15992380-8	2005	p-Chloromercuribenzoic acid and cetyltrimethylammonium chloride, which inhibited recombinant NAPE-PLD dose-dependently, strongly inhibited the enzyme of all the brain regions.	Cetrimonium	32-63	N-acyl phosphatidylethanolamine phospholipase D	Rattus norvegicus	93-101
15792874-6	2005	UV irradiation (365 nm) of solutions containing DNDI and the redox protein cytochrome c (cyt c) resulted in the reduction of the heme iron from the Fe(III) to the Fe(II) state, a reaction that was inhibited by the incorporation of DNDI into CTAB micelles.	Cetrimonium	241-245	cytochrome c, somatic	Homo sapiens	75-87
15969813-1	2005	In situ Fourier transform infrared internal reflection spectroscopy (FT-IR/IRS) was used to calculate the adsorption density values for spherical cetyltrimethylammonium bromide (CTAB) micelles at the silica/silicon (SiO2/Si) surface based on a previously developed adsorption density equation.	Cetrimonium	146-176	isoleucyl-tRNA synthetase 1	Homo sapiens	69-78
15969813-1	2005	In situ Fourier transform infrared internal reflection spectroscopy (FT-IR/IRS) was used to calculate the adsorption density values for spherical cetyltrimethylammonium bromide (CTAB) micelles at the silica/silicon (SiO2/Si) surface based on a previously developed adsorption density equation.	Cetrimonium	178-182	isoleucyl-tRNA synthetase 1	Homo sapiens	69-78
15837498-2	2005	ethanolamine, diethanolamine, and triethanolamine, by N-bromosuccinimide (NBS) in alkaline medium has been investigated in the absence as well as in the presence of cetyltrimethylammonium bromide (CTAB), a cationic surfactant.	Cetrimonium	197-201	nibrin	Homo sapiens	74-77
16851908-8	2005	The location of SL1SiEt throughout the formation process was obtained from electron spin-echo envelope modulation (ESEEM) measurements on MCM-41 prepared with CTAB deuterated either at the N-methyl or the alpha position and in a reaction carried out in D2O.	Cetrimonium	159-163	TATA-box binding protein associated factor, RNA polymerase I subunit A	Homo sapiens	16-19
15792874-6	2005	UV irradiation (365 nm) of solutions containing DNDI and the redox protein cytochrome c (cyt c) resulted in the reduction of the heme iron from the Fe(III) to the Fe(II) state, a reaction that was inhibited by the incorporation of DNDI into CTAB micelles.	Cetrimonium	241-245	cytochrome c, somatic	Homo sapiens	89-94
15988721-5	2005	The experimental results demonstrate that the N-terminal trimethylammonium derivatives of peptides exhibit MALDI signals comparable to or exceeding those of arginine-containing standards such as angiotensin I.	Cetrimonium	57-74	angiotensinogen	Homo sapiens	195-208
15796511-1	2005	SANS measurements revealed that polyelectrolytes, sodium salt of partially sulfonated polystyrenes, incorporated into enormously long hybrid threadlike micelles formed in aqueous solution with a cationic surfactant, cetyltrimethylammonium bromide, have a highly extended conformation with high confinement along the micelles with a radius of 2.3 nm.	Cetrimonium	216-246	USH1 protein network component sans	Homo sapiens	0-4
15721936-5	2005	The observed decrease in the values of G(0) and eta(0) at higher concentrations of silica particles is explained in terms of the formation of surfactant bilayers due to the adsorption of the positively charged cetyl trimethylammonium to the negatively charged silica.	Cetrimonium	210-233	endothelin receptor type A	Homo sapiens	48-51
15506760-1	2004	Positively charged trimethylammonium-functionalized mixed monolayer protected clusters (MMPCs) of different chain lengths (C(8) and C(11)) have been used to bind beta-galactosidase through complementary electrostatic interactions, resulting in complete enzyme inhibition.	Cetrimonium	19-36	aldo-keto reductase family 1 member C4	Homo sapiens	132-137
15506760-1	2004	Positively charged trimethylammonium-functionalized mixed monolayer protected clusters (MMPCs) of different chain lengths (C(8) and C(11)) have been used to bind beta-galactosidase through complementary electrostatic interactions, resulting in complete enzyme inhibition.	Cetrimonium	19-36	galactosidase beta 1	Homo sapiens	162-180
15298386-1	2004	We describe here a new approach to the synthesis of size-controllable polypyrrole/carbon nanotube (CNT) nanocables by in situ chemical oxidative polymerization directed by the cationic surfactant cetyltrimethylammonium bromide (CTAB) or the nonionic surfactant polyethylene glycol mono-p-nonylphenyl ether (Opi-10).	Cetrimonium	196-226	heat shock protein nuclear import factor hikeshi	Homo sapiens	307-313
15243734-2	2004	The procedure exploits the enhancement of the cobalt peak obtained by use of the system Co(II)-dimethylglyoxime-piperazine-1,4-bis(2-ethanesulfonic acid)-cetyltrimethylammonium bromide.	Cetrimonium	154-184	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	88-93
15274559-7	2004	Above the cmc, however, the CTAOH reaction again proceeded solely via the SN2(P) pathway while both pathways were operative with CTAMINA.	Cetrimonium	28-33	solute carrier family 38 member 5	Homo sapiens	74-77
15274595-4	2004	On the basis of FE-SEM, BET, and XRD analyses, the increases are attributed to decreased particle size, improved interparticle connectivity, and enhanced crystallinity of the CTAB-promoted TiO2 particles and decreased void volume in the film.	Cetrimonium	175-179	delta/notch like EGF repeat containing	Homo sapiens	24-27
15301951-2	2004	CNT (dispersed in the solution of 0.1% CTAB) has promotion effects on the direct electron transfer of glucose oxidase (GOx), which was immobilized onto the surface of CNT.	Cetrimonium	39-43	hydroxyacid oxidase 1	Homo sapiens	102-117
15301951-2	2004	CNT (dispersed in the solution of 0.1% CTAB) has promotion effects on the direct electron transfer of glucose oxidase (GOx), which was immobilized onto the surface of CNT.	Cetrimonium	39-43	hydroxyacid oxidase 1	Homo sapiens	119-122
14656519-3	2003	Above pH 8.0, the peak current of first wave Pc1 of DISS was enhanced in the presence of cetyltrimethylammonium bromide (CTAB).	Cetrimonium	89-119	polycystin 1, transient receptor potential channel interacting	Homo sapiens	45-48
15068284-1	2004	The fluorescence emission spectra and 3D fluorescence spectra of bovine serum albumin (BSA) in cetyltrimethylammonium bromide (CTAB) reversed micelles were affected by the microenvironment.	Cetrimonium	95-125	albumin	Homo sapiens	72-85
15068284-1	2004	The fluorescence emission spectra and 3D fluorescence spectra of bovine serum albumin (BSA) in cetyltrimethylammonium bromide (CTAB) reversed micelles were affected by the microenvironment.	Cetrimonium	127-131	albumin	Homo sapiens	72-85
14753787-7	2004	Excellent linear relationship was obtained with correlation coefficient of 0.9998 for alpha-lactalbumin concentration ranging from 3.91 x 10(-7) to 1.25 x 10(-5) M. Separation of protein standards at low pH was also demonstrated by reversing the electroosmotic flow (EOF) with addition of cetyltrimethylammonium bromide (CTAB) to the running buffer.	Cetrimonium	289-319	lactalbumin alpha	Homo sapiens	86-103
14753787-7	2004	Excellent linear relationship was obtained with correlation coefficient of 0.9998 for alpha-lactalbumin concentration ranging from 3.91 x 10(-7) to 1.25 x 10(-5) M. Separation of protein standards at low pH was also demonstrated by reversing the electroosmotic flow (EOF) with addition of cetyltrimethylammonium bromide (CTAB) to the running buffer.	Cetrimonium	321-325	lactalbumin alpha	Homo sapiens	86-103
14656519-3	2003	Above pH 8.0, the peak current of first wave Pc1 of DISS was enhanced in the presence of cetyltrimethylammonium bromide (CTAB).	Cetrimonium	121-125	polycystin 1, transient receptor potential channel interacting	Homo sapiens	45-48
14656519-5	2003	In Britton-Robinson buffer solution (pH 11.7) containing 9.4 x 10(-6)mol L(-1) CTAB, the peak potential of first wave Pc1 of DISS was -1.59 V (vs standard saturated calomel electrode) and its first-order derivative peak current was proportional to the concentration of DISS in the range 5.0 x 10(-8)-6.0 x 10(-7)mol L(-1) (r=0.998).	Cetrimonium	79-83	polycystin 1, transient receptor potential channel interacting	Homo sapiens	118-121
12643738-5	2003	A remarkably high radiochemical yield (>90%) was achieved for the F-18 nucleophilic aromatic substitution under mild conditions (room temperature in less than 10 min), indicating the structural advantage of the designed molecule to facilitate the F-18 for trimethylammonium substitution in the presence of two electron-withdrawing groups (nitrile and carbonyl).	Cetrimonium	259-276	mastermind like domain containing 1	Homo sapiens	69-73
16256532-0	2003	Surfactant displacement of human serum albumin adsorbed on loosely packed self-assembled monolayers: cetyltrimethylammonium bromide versus sodium dodecyl sulfate.	Cetrimonium	101-131	albumin	Homo sapiens	33-46
16256532-1	2003	The surfactants sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB) displace human serum albumin (HSA) from loosely packed self-assembled monolayers (SAM) of hydrophobic alkyl chains by different means.	Cetrimonium	49-79	albumin	Homo sapiens	102-115
16256532-1	2003	The surfactants sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB) displace human serum albumin (HSA) from loosely packed self-assembled monolayers (SAM) of hydrophobic alkyl chains by different means.	Cetrimonium	81-85	albumin	Homo sapiens	102-115
14643300-2	2003	A novel HIV vaccine composed of plasmid DNA-encoding p55 gag formulated with poly-lactide-co-glycolide microparticles (PLG) and cetyl trimethyl ammonium bromide (CTAB) elicits both serum antibody titers and cytotoxic lymphocyte activity in mice at doses two orders of magnitude lower than those required for comparable response to plasmid DNA in saline.	Cetrimonium	128-160	membrane protein, palmitoylated	Mus musculus	53-56
12720352-3	2003	In this work, trimethylammonium salts of undecachlorinated (UCC), undecabrominated (UBC), hexabrominated (HBC), and undecaiodinated (UIC) carborane anions were prepared and evaluated for their potential use in solvent polymeric membrane-based sensors.	Cetrimonium	14-31	ubiquitin C	Homo sapiens	84-87
12720352-3	2003	In this work, trimethylammonium salts of undecachlorinated (UCC), undecabrominated (UBC), hexabrominated (HBC), and undecaiodinated (UIC) carborane anions were prepared and evaluated for their potential use in solvent polymeric membrane-based sensors.	Cetrimonium	14-31	keratin 88, pseudogene	Homo sapiens	106-109
12643738-5	2003	A remarkably high radiochemical yield (>90%) was achieved for the F-18 nucleophilic aromatic substitution under mild conditions (room temperature in less than 10 min), indicating the structural advantage of the designed molecule to facilitate the F-18 for trimethylammonium substitution in the presence of two electron-withdrawing groups (nitrile and carbonyl).	Cetrimonium	259-276	mastermind like domain containing 1	Homo sapiens	250-254
12636163-0	2003	The effect of CTAB concentration in cationic PLG microparticles on DNA adsorption and in vivo performance.	Cetrimonium	14-18	plasminogen	Homo sapiens	45-48
12234608-2	2002	Of these compounds, the dimethyl derivative (DIMATE) was a competitive irreversible inhibitor (K(i) approximately 280 microM) of baker"s yeast ALDH1 in vitro showing 80% inhibition at 400 microM when preincubated with the enzyme for 30min, whereas the trimethyl ammonium and the morpholine derivatives showed only 15% inhibition at 600 microM even after 60min preincubation.	Cetrimonium	252-270	aldehyde dehydrogenase family 1, subfamily A1	Mus musculus	143-148
12511091-2	2002	Proteins including bovine serum albumin (BSA), human serum albumin (HSA) can combine with morin and cetyltrimethylammonium briomide (CTMAB) in the pH range 7.0-8.0 and produce enhanced RDLS signal at lambda(ex)/lambda(em) 305.0/610.0 nm.	Cetrimonium	133-138	albumin	Homo sapiens	26-39
12511091-2	2002	Proteins including bovine serum albumin (BSA), human serum albumin (HSA) can combine with morin and cetyltrimethylammonium briomide (CTMAB) in the pH range 7.0-8.0 and produce enhanced RDLS signal at lambda(ex)/lambda(em) 305.0/610.0 nm.	Cetrimonium	133-138	albumin	Homo sapiens	53-66
18968778-2	2002	The QADEAB can react with Co(II) in the presence of pH 3.8 acetic acid-sodium acetate buffer solution and cetyl trimethylammonium bromide (CTMAB) medium to form a violet chelate of a molar ratio 1:2 (cobalt to QADEAB).	Cetrimonium	139-144	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	26-32
12128183-1	2002	I. Microcalorimetric investigation on the interaction of cetyltrimethylammonium bromide (CTAB) and sodium dodecylsulfate (SDS) with gelatin (Gn), lysozyme (Lz) and deoxyribonucleic acid (DNA).	Cetrimonium	57-87	lysozyme	Homo sapiens	146-154
18968778-2	2002	The QADEAB can react with Co(II) in the presence of pH 3.8 acetic acid-sodium acetate buffer solution and cetyl trimethylammonium bromide (CTMAB) medium to form a violet chelate of a molar ratio 1:2 (cobalt to QADEAB).	Cetrimonium	106-137	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	26-32
12128183-1	2002	I. Microcalorimetric investigation on the interaction of cetyltrimethylammonium bromide (CTAB) and sodium dodecylsulfate (SDS) with gelatin (Gn), lysozyme (Lz) and deoxyribonucleic acid (DNA).	Cetrimonium	57-87	lysozyme	Homo sapiens	156-158
12128183-1	2002	I. Microcalorimetric investigation on the interaction of cetyltrimethylammonium bromide (CTAB) and sodium dodecylsulfate (SDS) with gelatin (Gn), lysozyme (Lz) and deoxyribonucleic acid (DNA).	Cetrimonium	89-93	lysozyme	Homo sapiens	146-154
12128183-1	2002	I. Microcalorimetric investigation on the interaction of cetyltrimethylammonium bromide (CTAB) and sodium dodecylsulfate (SDS) with gelatin (Gn), lysozyme (Lz) and deoxyribonucleic acid (DNA).	Cetrimonium	89-93	lysozyme	Homo sapiens	156-158
12128183-2	2002	The interaction of the surfactants cetyltrimethyl ammonium bromide (CTAB) and sodium dodecyl sulfate (SDS) with the biopolymers gelatin (Gn), lysozyme (Lz) and deoxyribonucleic acid (DNA) was studied by isothermal titration microcalorimetry at varied biopolymer concentration, pH and temperature.	Cetrimonium	35-66	lysozyme	Homo sapiens	142-150
12128183-2	2002	The interaction of the surfactants cetyltrimethyl ammonium bromide (CTAB) and sodium dodecyl sulfate (SDS) with the biopolymers gelatin (Gn), lysozyme (Lz) and deoxyribonucleic acid (DNA) was studied by isothermal titration microcalorimetry at varied biopolymer concentration, pH and temperature.	Cetrimonium	35-66	lysozyme	Homo sapiens	152-154
12128183-2	2002	The interaction of the surfactants cetyltrimethyl ammonium bromide (CTAB) and sodium dodecyl sulfate (SDS) with the biopolymers gelatin (Gn), lysozyme (Lz) and deoxyribonucleic acid (DNA) was studied by isothermal titration microcalorimetry at varied biopolymer concentration, pH and temperature.	Cetrimonium	68-72	lysozyme	Homo sapiens	142-150
10508927-0	1999	Escherichia coli TEM1 beta-lactamase in CTAB reverse micelles: exchange/diffusion-limited catalysis.	Cetrimonium	40-44	TEM-1 beta-lactamase	Escherichia coli	17-36
12152307-1	2002	The biochemical method for determination of cetyltrimethyl ammonium or cetylpyridinium, both being nitrogenated cationic surfactants, has been devised by using horse blood serum butyrylcholinesterase as analytical reagent.	Cetrimonium	44-67	butyrylcholinesterase	Homo sapiens	178-199
11697193-4	2001	Also, .UH- is reduced by flavonoids, quercetin and rutin in CTAB micelles at rate constants of 6 x 10(6) M-1s-1 and 1 x 10(6) M-1s-1, respectively.	Cetrimonium	60-64	tumor associated calcium signal transducer 2	Homo sapiens	105-132
10733879-2	2000	Initial studies showed the bulk of peroxidase-positive myeloperoxidase activity to be located in the cetyltrimethylammonium bromide solubilized particulate fraction of cell homogenates.	Cetrimonium	101-131	myeloperoxidase	Homo sapiens	55-70
11448219-2	2001	Derivative 27 (ZR = -HNSO(2)R, R = C(12), X = trimethylammonium, Y = carboxylate, (R) form) showed the highest activity (IC(50) = 0.7 microM) along with a good selectivity (M-CPT I/L-CPTI IC(50) ratio = 4.86).	Cetrimonium	46-63	carnitine palmitoyltransferase 1B	Rattus norvegicus	175-180
10925724-4	2000	In an attempt to use this method in leukocytes measuring in stool, fecal MPO was solubilized with hexadecyltrimethylammonium bromide and the MPO activity was measured by a dianisidine-H2O2 assay.	Cetrimonium	98-132	myeloperoxidase	Homo sapiens	73-76
10447935-11	1999	Our study shows that CTAB is an effective detergent for lysing granulocytes, yielding high and reproducible recovery rates of ECP and MPO.	Cetrimonium	21-25	ribonuclease A family member 3	Homo sapiens	126-129
10447935-11	1999	Our study shows that CTAB is an effective detergent for lysing granulocytes, yielding high and reproducible recovery rates of ECP and MPO.	Cetrimonium	21-25	myeloperoxidase	Homo sapiens	134-137
12935496-2	1999	We tried to type one of the nuclear DNA loci, HLA-DQA1, from hair shafts, using an efficient cetyl-trimethyl ammonium bromide (CTAB) precipitation for DNA purification and a sensitive semi-nested PCR.	Cetrimonium	93-125	major histocompatibility complex, class II, DQ alpha 1	Homo sapiens	46-54
10415112-2	1999	The ch-DHFR entrapped in CTAB and DAB reverse micelles shows very low activity at a lower ratio of water to surfactant (omega(0)).	Cetrimonium	25-29	dihydrofolate reductase	Cricetulus griseus	7-11
10415112-5	1999	Only a slight change in emission intensity of ch-DHFR accompanies enzyme activation in the presence of low concentrations of guanidine hydrochloride in CTAB and DAB reverse micelles.	Cetrimonium	152-156	dihydrofolate reductase	Cricetulus griseus	49-53
15818961-1	1999	A new fluorometric method has been developed for the determination of trace zirconium, based on the fluorescence quenching effect of Zr (IV)-5"-nitro-salicylfluorone (5"-N-SAF)-hexadecyltrimethylammonium bromide (CTMAB).	Cetrimonium	213-218	FAS antisense RNA 1	Homo sapiens	172-175
12935496-2	1999	We tried to type one of the nuclear DNA loci, HLA-DQA1, from hair shafts, using an efficient cetyl-trimethyl ammonium bromide (CTAB) precipitation for DNA purification and a sensitive semi-nested PCR.	Cetrimonium	127-131	major histocompatibility complex, class II, DQ alpha 1	Homo sapiens	46-54
9924975-2	1998	First, PKC alpha antisense oligonucleotides were associated with polyisobutylcyanoacrylate (PIBCA) nanoparticles pre-coated with cetyltrimethyl ammonium bromide (CTAB), a hydrophobic cation.	Cetrimonium	129-160	protein kinase C alpha	Homo sapiens	7-16
9924975-2	1998	First, PKC alpha antisense oligonucleotides were associated with polyisobutylcyanoacrylate (PIBCA) nanoparticles pre-coated with cetyltrimethyl ammonium bromide (CTAB), a hydrophobic cation.	Cetrimonium	162-166	protein kinase C alpha	Homo sapiens	7-16
9540975-9	1998	Both sodium dodecyl sulfate and CTAB were found to cause induction and upregulation of SKALP and involucrin at low doses following a 24 h patch test, whereas high concentrations of Triton X-100 did not.	Cetrimonium	32-36	peptidase inhibitor 3	Homo sapiens	87-92
24414897-4	1995	When Fraction A-2 was treated with cetyltrimethylammonium hydroxide and chloroform/butanol (24:1, v/v), it behaved as a proteinbound polysaccharide, with a molecular mass estimated to be 154 kDa by gel filtration.	Cetrimonium	35-67	G protein-coupled receptor 162	Mus musculus	14-17
18967059-1	1998	Mesoporous SnO(2) with high surface areas were synthesized using a cationic surfactant (N-cetyl-N,N,N-trimethylammonium bromide) as a synthetic template.	Cetrimonium	88-127	strawberry notch homolog 1	Homo sapiens	11-14
9241227-2	1997	181, 476 (1996)) concerned with the adsorption of hexadecyltrimethylammonium bromide (CTAB) on mica, using rates of evaporation ( approximately 0.07 mm/h) measured for that setup.	Cetrimonium	50-84	MHC class I polypeptide-related sequence A	Homo sapiens	95-99
9241227-2	1997	181, 476 (1996)) concerned with the adsorption of hexadecyltrimethylammonium bromide (CTAB) on mica, using rates of evaporation ( approximately 0.07 mm/h) measured for that setup.	Cetrimonium	86-90	MHC class I polypeptide-related sequence A	Homo sapiens	95-99
8979370-1	1996	The anti-desmin monoclonal antibodies (MAbs) DSB389, AC54, and DSB860 recognize intermediate filaments (IFs) and nuclear antigens that appear granular, locate around chromosomes, and are insoluble following 0.5% Triton X-100 and cetyltrimethylammonium bromide (CTAB) extraction.	Cetrimonium	229-259	desmin	Homo sapiens	9-15
8979370-1	1996	The anti-desmin monoclonal antibodies (MAbs) DSB389, AC54, and DSB860 recognize intermediate filaments (IFs) and nuclear antigens that appear granular, locate around chromosomes, and are insoluble following 0.5% Triton X-100 and cetyltrimethylammonium bromide (CTAB) extraction.	Cetrimonium	261-265	desmin	Homo sapiens	9-15
8939006-7	1996	Treatment of the mitochondrial suspension with sodium deoxycholate, CTAB, Lubrol XW, Brij 58, Emulgen 913 and Triton X-100 markedly decreased the 3 beta-HSD activities as a function of the detergent concentration and failed in to achieve solubilization.	Cetrimonium	68-72	3 beta-hydroxysteroid dehydrogenase/Delta 5-->4-isomerase	Canis lupus familiaris	146-156
9741392-7	1998	Optimal recovery of myeloperoxidase activity (>twofold increase) was achieved only with two sequential extractions using 50 mM phosphate buffer (pH 7.4) containing 10 mM N-ethylmaleimide, and subsequent solubilization of myeloperoxidase activity by extraction with 0.5% hexadecyltrimethylammonium bromide in 50 mM phosphate buffer (pH 6.0).	Cetrimonium	273-307	myeloperoxidase	Rattus norvegicus	20-35
18574729-5	1998	The amount of macropores and the enzymatic activity of the lipoxygenase-phyllosilicate composites increased with an increase in the ratio of trimethylammonium (TMA)-phyllosilicate to cross-linking reagent TMOS.	Cetrimonium	141-158	linoleate 9S-lipoxygenase-4	Glycine max	59-71
9176201-3	1997	Increasing the resting pHi with ammonium chloride (5-20 mM), trimethylammonium (2-10 mM), or triethylammonium (1.2-8 mM) reduced the frequency of oscillations.	Cetrimonium	61-78	glucose-6-phosphate isomerase	Rattus norvegicus	23-26
7582300-2	1995	We have developed a simple method for distinguishing the antiprotease activities of SLPI and elafin in lung lavage fluid from those of alpha 1-antitrypsin (alpha 1-AT) that is based on the resistance of the low-molecular-weight antiproteases to inactivation by cetyltrimethylammonium bromide.	Cetrimonium	261-291	secretory leukocyte peptidase inhibitor	Homo sapiens	84-88
7582300-2	1995	We have developed a simple method for distinguishing the antiprotease activities of SLPI and elafin in lung lavage fluid from those of alpha 1-antitrypsin (alpha 1-AT) that is based on the resistance of the low-molecular-weight antiproteases to inactivation by cetyltrimethylammonium bromide.	Cetrimonium	261-291	serpin family A member 1	Homo sapiens	156-166
7631012-6	1995	Our results show that the surfactant cetyltrimethylammonium bromide (CTAB) can mimic the ATX-70-induced increase in the TMP-NO signal, but it fails to reproduce the behavior of ATX-70 in D2O: while the yields of TMP-NO in the presence of ATX-70 increase in D2O, the opposite effect was found with the surfactant CTAB.	Cetrimonium	37-67	ectonucleotide pyrophosphatase/phosphodiesterase 2	Homo sapiens	89-92
7631012-6	1995	Our results show that the surfactant cetyltrimethylammonium bromide (CTAB) can mimic the ATX-70-induced increase in the TMP-NO signal, but it fails to reproduce the behavior of ATX-70 in D2O: while the yields of TMP-NO in the presence of ATX-70 increase in D2O, the opposite effect was found with the surfactant CTAB.	Cetrimonium	69-73	ectonucleotide pyrophosphatase/phosphodiesterase 2	Homo sapiens	89-92
7631012-6	1995	Our results show that the surfactant cetyltrimethylammonium bromide (CTAB) can mimic the ATX-70-induced increase in the TMP-NO signal, but it fails to reproduce the behavior of ATX-70 in D2O: while the yields of TMP-NO in the presence of ATX-70 increase in D2O, the opposite effect was found with the surfactant CTAB.	Cetrimonium	312-316	ectonucleotide pyrophosphatase/phosphodiesterase 2	Homo sapiens	89-92
8553471-1	1995	Cetyltrimethyl ammonium and cetylpyridinium, both being cationic detergents, have been studied for their effect on the catalytic activity of horse blood serum cholinesterase (BuHChE) in reactions of hydrolysis of carbonic acid esters.	Cetrimonium	0-23	butyrylcholinesterase	Homo sapiens	159-173
8779278-2	1995	Conformational and geometrical properties of the hexamethylenebis(trimethylammonium) (CH3)3N+-(CH2)6)-N+(CH3)3 (hexamethonium) and its derivatives with various degree of conformational flexibility of interonion chain having disulfide or two dimethylsilane groups or difluoromethylene chain instead of cholinesterase reversible inhibitors have been determined using molecular mechanics methods.	Cetrimonium	66-83	butyrylcholinesterase	Homo sapiens	301-315
7859162-2	1994	The system, referred to as CAT gel electrophoresis, uses the detergent cetyltrimethylammonium bromide in combination with a discontinuous gel matrix to resolve protein mixtures into discrete bands.	Cetrimonium	71-101	catalase	Homo sapiens	27-30
7895717-3	1994	Both sodium dodecyl sulfate (SDS) and cetyltrime-thylammonium bromide (CTAB) in the electrophoretic medium were found to improve the separation of the PTH-amino acids compared to the use of CTAB or SDS alone.	Cetrimonium	38-69	parathyroid hormone	Homo sapiens	151-154
7895717-3	1994	Both sodium dodecyl sulfate (SDS) and cetyltrime-thylammonium bromide (CTAB) in the electrophoretic medium were found to improve the separation of the PTH-amino acids compared to the use of CTAB or SDS alone.	Cetrimonium	71-75	parathyroid hormone	Homo sapiens	151-154
7895717-4	1994	Complete separation of the PTH amino acids was achieved using a buffer containing 2.5 mM CTAB and 40 mM SDS.	Cetrimonium	89-93	parathyroid hormone	Homo sapiens	27-30
7822268-1	1994	A trypsin-like protease was extracted with 1% cetyltrimethylammonium bromide (CTAB) at pH 7.0 from boar cauda epididymal sperm nuclei whose acrosin had previously been removed by acid extraction.	Cetrimonium	46-76	kallikrein related peptidase 11	Homo sapiens	2-23
7822268-1	1994	A trypsin-like protease was extracted with 1% cetyltrimethylammonium bromide (CTAB) at pH 7.0 from boar cauda epididymal sperm nuclei whose acrosin had previously been removed by acid extraction.	Cetrimonium	78-82	kallikrein related peptidase 11	Homo sapiens	2-23
7822268-1	1994	A trypsin-like protease was extracted with 1% cetyltrimethylammonium bromide (CTAB) at pH 7.0 from boar cauda epididymal sperm nuclei whose acrosin had previously been removed by acid extraction.	Cetrimonium	78-82	acrosin	Homo sapiens	140-147
7819219-3	1995	TPI denatured with guanidine hydrochloride undergoes reactivation in reverse micelles formed with n-octane, hexanol, cetyltrimethylammonium bromide, and water.	Cetrimonium	117-147	triosephosphate isomerase	Oryctolagus cuniculus	0-3
7881182-2	1994	This enzyme is a soluble cytochrome b5-dependent monooxygenase and has been purified to apparent homogeneity from pig submandibular glands by precipitation with N-cetyl-N,N,N-trimethylammonium bromide and fractionation on Q-Sepharose, Cibacron Blue 3GA-Agarose, Reactive Brown 10-Agarose, Hexyl-Agarose and Superose S.12.	Cetrimonium	161-200	cytochrome b5 type A	Sus scrofa	25-38
8186252-2	1994	We describe the conformational changes associated with the binding of a surfactant, cetyltrimethylammonium chloride (CTAC) to recombinant porcine growth hormone (PGH).	Cetrimonium	84-115	growth hormone 1	Homo sapiens	146-160
8186252-2	1994	We describe the conformational changes associated with the binding of a surfactant, cetyltrimethylammonium chloride (CTAC) to recombinant porcine growth hormone (PGH).	Cetrimonium	117-121	growth hormone 1	Homo sapiens	146-160
7511692-7	1994	The trimethylammonium salts of the complexes were tested for their ability to inhibit the interaction between gp120 and CD4 using a cell-free system.	Cetrimonium	4-21	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	110-115
7511692-7	1994	The trimethylammonium salts of the complexes were tested for their ability to inhibit the interaction between gp120 and CD4 using a cell-free system.	Cetrimonium	4-21	CD4 molecule	Homo sapiens	120-123
7817652-1	1994	Conformational properties of a series of polymethylenebis (trimethylammonium) derivatives [formula: see text] (n = 4-10), cholinesterase reversible inhibitors, were studied by molecular mechanics method.	Cetrimonium	59-76	butyrylcholinesterase	Homo sapiens	122-136
7764009-2	1993	Alcohol dehydrogenase (ADH), glucose-6-phosphate dehydrogenase (G6PDH), hexokinase (HK), and beta-galactosidase (beta-GAL) activities of cetyltrimethylammonium bromide (CTAB)-permeabilized whole yeast cells were employed to estimate ethyl alcohol, glucose, and lactose.	Cetrimonium	137-167	glucose-6-phosphate dehydrogenase	Saccharomyces cerevisiae S288C	29-62
7764353-1	1993	Recombinant cytochrome b5 was extracted to a reversed micelle phase of a cationic surfactant (hexadecyltrimethylammonium bromide, CTAB) in cyclohexane/decanol and back-extracted to a fresh aqueous phase.	Cetrimonium	94-128	cytochrome b5 type A	Homo sapiens	12-25
7764353-1	1993	Recombinant cytochrome b5 was extracted to a reversed micelle phase of a cationic surfactant (hexadecyltrimethylammonium bromide, CTAB) in cyclohexane/decanol and back-extracted to a fresh aqueous phase.	Cetrimonium	130-134	cytochrome b5 type A	Homo sapiens	12-25
7968515-11	1993	B. subtilis CtaB, which is homologous to Saccharomyces cerevisiae COX10 and E. coli CyoE, also has a role in haem A synthesis and seems to be required for both cytochrome a and cytochrome o synthesis.	Cetrimonium	12-16	protoheme IX farnesyltransferase	Saccharomyces cerevisiae S288C	66-71
7764009-2	1993	Alcohol dehydrogenase (ADH), glucose-6-phosphate dehydrogenase (G6PDH), hexokinase (HK), and beta-galactosidase (beta-GAL) activities of cetyltrimethylammonium bromide (CTAB)-permeabilized whole yeast cells were employed to estimate ethyl alcohol, glucose, and lactose.	Cetrimonium	137-167	glucose-6-phosphate dehydrogenase	Saccharomyces cerevisiae S288C	64-69
7764009-2	1993	Alcohol dehydrogenase (ADH), glucose-6-phosphate dehydrogenase (G6PDH), hexokinase (HK), and beta-galactosidase (beta-GAL) activities of cetyltrimethylammonium bromide (CTAB)-permeabilized whole yeast cells were employed to estimate ethyl alcohol, glucose, and lactose.	Cetrimonium	137-167	hexokinase	Saccharomyces cerevisiae S288C	72-82
7764009-2	1993	Alcohol dehydrogenase (ADH), glucose-6-phosphate dehydrogenase (G6PDH), hexokinase (HK), and beta-galactosidase (beta-GAL) activities of cetyltrimethylammonium bromide (CTAB)-permeabilized whole yeast cells were employed to estimate ethyl alcohol, glucose, and lactose.	Cetrimonium	137-167	hexokinase	Saccharomyces cerevisiae S288C	84-86
7764009-2	1993	Alcohol dehydrogenase (ADH), glucose-6-phosphate dehydrogenase (G6PDH), hexokinase (HK), and beta-galactosidase (beta-GAL) activities of cetyltrimethylammonium bromide (CTAB)-permeabilized whole yeast cells were employed to estimate ethyl alcohol, glucose, and lactose.	Cetrimonium	169-173	glucose-6-phosphate dehydrogenase	Saccharomyces cerevisiae S288C	64-69
7764009-2	1993	Alcohol dehydrogenase (ADH), glucose-6-phosphate dehydrogenase (G6PDH), hexokinase (HK), and beta-galactosidase (beta-GAL) activities of cetyltrimethylammonium bromide (CTAB)-permeabilized whole yeast cells were employed to estimate ethyl alcohol, glucose, and lactose.	Cetrimonium	169-173	hexokinase	Saccharomyces cerevisiae S288C	72-82
8482489-6	1993	These results suggest that it is possible to enhance the binding of the permanently charged trimethylammonium analog of chlorpromazine by the addition of a functional group near the quaternary nitrogen which is capable of forming a hydrogen bond with the D2 dopamine receptor.	Cetrimonium	92-109	dopamine receptor D2	Homo sapiens	255-275
1457731-6	1992	Only the positively charged hexadecyltrimethylammonium hydroxide provokes the collapse of the vesicles into mixed micelles with concomitant altered dislocation of the gastrin-peptide in the new aggregational state.	Cetrimonium	28-64	gastrin	Homo sapiens	167-174
1325820-1	1992	Myeloperoxidase was solubilized with hexadecyltrimethylammonium bromide and myeloperoxidase activity was measured with a dianisidine-H2O2 assay in the ischemic area after middle cerebral artery occlusion in rats.	Cetrimonium	37-71	myeloperoxidase	Rattus norvegicus	0-15
1963456-8	1990	The resulting 30,000 g pellets expressed MPO activity after suspending them in 50 mM PB containing 0.5% hexadecyltrimethylammoniumbromide (HTAB).	Cetrimonium	104-137	myeloperoxidase	Rattus norvegicus	41-44
1776672-1	1991	Alcohol dehydrogenase (ADH) and glucose-6-phosphate dehydrogenase (G6PDH) activities of cetyltrimethylammonium bromide permeabilized baker"s yeast whole cells were employed to prepare reduced nicotinamide nucleotides NADH and NADPH from their corresponding oxidised forms.	Cetrimonium	88-118	glucose-6-phosphate dehydrogenase	Saccharomyces cerevisiae S288C	32-65
1776672-1	1991	Alcohol dehydrogenase (ADH) and glucose-6-phosphate dehydrogenase (G6PDH) activities of cetyltrimethylammonium bromide permeabilized baker"s yeast whole cells were employed to prepare reduced nicotinamide nucleotides NADH and NADPH from their corresponding oxidised forms.	Cetrimonium	88-118	glucose-6-phosphate dehydrogenase	Saccharomyces cerevisiae S288C	67-72
1701376-7	1990	Incorporation of the plasma tracers ([3H]glucose and [35S]sodium sulfate) into mucin derived from hexadecyltrimethylammonium bromide precipitation after treatment with ASA (100 mg/kg body wt) decreased, although administration of dimethylprostaglandin E2 (100 micrograms/kg body wt) significantly increased the specific tracer incorporation values for the sialomucin and sulfomucin indices in luminal mucin fractions.	Cetrimonium	98-132	solute carrier family 13 member 2	Rattus norvegicus	79-84
1963456-8	1990	The resulting 30,000 g pellets expressed MPO activity after suspending them in 50 mM PB containing 0.5% hexadecyltrimethylammoniumbromide (HTAB).	Cetrimonium	139-143	myeloperoxidase	Rattus norvegicus	41-44
1965503-4	1990	White blood cells, isolated freshly from normal donors, were lysed with cetyltrimethylammonium bromide to liberate myeloperoxidase.	Cetrimonium	72-102	myeloperoxidase	Homo sapiens	115-130
3233222-3	1988	Membranes composed of a mixture of phosphatidylcholine (PC) and positively charged lipids like stearylamine, sphingosine, or hexadecyltrimethylammonium bromide caused a more than 1000-fold increase of the rate of prothrombin activation.	Cetrimonium	125-159	coagulation factor II, thrombin	Homo sapiens	213-224
2229231-2	1990	By using this mode of chromatography with a solution of cetyltrimethylammonium bromide as the displacer, the capacity of a reversed-phase column can be increased 50- to 100-fold for separation of a tryptic digest of biosynthetic human growth hormone.	Cetrimonium	56-86	growth hormone 1	Homo sapiens	235-249
34848464-8	2021	CONCLUSION: CTAB attenuates the mesenchymal characteristics through upregulation of TIMP3 by inhibiting the canonical TGF-beta/Smad/miR-181b/TIMP3 signaling involved in extracellular matrix remodeling in SCC4 cells and might be a promising anti-metastatic therapeutic agent for TSCC.	Cetrimonium	12-16	TIMP metallopeptidase inhibitor 3	Homo sapiens	84-89
34808196-0	2022	A reduced graphene oxide-Fe3O4 composite functionalized with cetyltrimethylammonium bromide for efficient adsorption of SARS-CoV-2 spike pseudovirus and human enteric viruses.	Cetrimonium	61-91	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	131-136
34808196-2	2022	In this study, reduced graphene oxide (rGO)-Fe3O4 nanoparticles were decorated with cetyltrimethylammonium bromide (CTAB) to adsorb severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike pseudovirus and three human enteric viruses (HuNoV, HRV, and HAdV).	Cetrimonium	84-114	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	193-198
34808196-2	2022	In this study, reduced graphene oxide (rGO)-Fe3O4 nanoparticles were decorated with cetyltrimethylammonium bromide (CTAB) to adsorb severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike pseudovirus and three human enteric viruses (HuNoV, HRV, and HAdV).	Cetrimonium	116-120	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	193-198
34808196-5	2022	CTAB-functionalized rGO-Fe3O4 exhibited exceptionally high adsorption of HuNoV, HRV, HAdV and SARS-CoV-2 spike pseudovirus, with maximum adsorption capacities of 3.55 x 107, 7.01 x 107, 2.21 x 107 and 6.92 x 106 genome copies mg-1, respectively.	Cetrimonium	0-4	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	105-110
34416581-1	2022	This work studies the Pb(II) removal onto bentonite clay modified by hexadecyl trimethyl ammonium bromide (HDTMA).	Cetrimonium	69-105	submaxillary gland androgen regulated protein 3B	Homo sapiens	22-28
34416581-1	2022	This work studies the Pb(II) removal onto bentonite clay modified by hexadecyl trimethyl ammonium bromide (HDTMA).	Cetrimonium	107-112	submaxillary gland androgen regulated protein 3B	Homo sapiens	22-28
34416581-8	2022	The FT-IR and TG-DSC analyses indicated that the formation of inner-sphere complexes plays a fundamental role in the mechanism of Pb(II) uptake onto HDTMA-bentonite clay.	Cetrimonium	149-154	submaxillary gland androgen regulated protein 3B	Homo sapiens	130-136
34416581-11	2022	In particular, we found a very interesting mechanism that the Pb(II) adsorption should occur inside the interlayer spaces of the HDTMA-bentonite.	Cetrimonium	129-134	submaxillary gland androgen regulated protein 3B	Homo sapiens	62-68
34273893-4	2021	The long alkane chain structure of cetyltrimethylammonium bromide (CTAB) and the quaternary ammonium salt structure of SCC have a high molecular affinity, so that the target molecule can show a strong and obvious characteristic signal of SERS.	Cetrimonium	35-65	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	238-242
34273893-4	2021	The long alkane chain structure of cetyltrimethylammonium bromide (CTAB) and the quaternary ammonium salt structure of SCC have a high molecular affinity, so that the target molecule can show a strong and obvious characteristic signal of SERS.	Cetrimonium	67-71	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	238-242
34848464-0	2021	Cetyltrimethylammonium Bromide Disrupts Mesenchymal Characteristics of Human Tongue Squamous Cell Carcinoma SCC4 Cells Through Modulating Canonical TGF-beta/Smad/miR-181b/TIMP3 Signaling Pathway.	Cetrimonium	0-30	transforming growth factor alpha	Homo sapiens	148-156
34848464-0	2021	Cetyltrimethylammonium Bromide Disrupts Mesenchymal Characteristics of Human Tongue Squamous Cell Carcinoma SCC4 Cells Through Modulating Canonical TGF-beta/Smad/miR-181b/TIMP3 Signaling Pathway.	Cetrimonium	0-30	TIMP metallopeptidase inhibitor 3	Homo sapiens	171-176
34848464-5	2021	CTAB reduced expression of matrix metalloproteinases (MMPs) such as MMP3, MMP7, and MMP14 in a concentration-dependent manner, while it increased expression of tissue inhibitors of metalloproteinase 3 (TIMP3).	Cetrimonium	0-4	matrix metallopeptidase 3	Homo sapiens	54-58
34848464-5	2021	CTAB reduced expression of matrix metalloproteinases (MMPs) such as MMP3, MMP7, and MMP14 in a concentration-dependent manner, while it increased expression of tissue inhibitors of metalloproteinase 3 (TIMP3).	Cetrimonium	0-4	matrix metallopeptidase 3	Homo sapiens	68-72
34848464-5	2021	CTAB reduced expression of matrix metalloproteinases (MMPs) such as MMP3, MMP7, and MMP14 in a concentration-dependent manner, while it increased expression of tissue inhibitors of metalloproteinase 3 (TIMP3).	Cetrimonium	0-4	matrix metallopeptidase 7	Homo sapiens	74-78
34848464-5	2021	CTAB reduced expression of matrix metalloproteinases (MMPs) such as MMP3, MMP7, and MMP14 in a concentration-dependent manner, while it increased expression of tissue inhibitors of metalloproteinase 3 (TIMP3).	Cetrimonium	0-4	matrix metallopeptidase 14	Homo sapiens	84-89
34848464-5	2021	CTAB reduced expression of matrix metalloproteinases (MMPs) such as MMP3, MMP7, and MMP14 in a concentration-dependent manner, while it increased expression of tissue inhibitors of metalloproteinase 3 (TIMP3).	Cetrimonium	0-4	TIMP metallopeptidase inhibitor 3	Homo sapiens	160-200
34848464-5	2021	CTAB reduced expression of matrix metalloproteinases (MMPs) such as MMP3, MMP7, and MMP14 in a concentration-dependent manner, while it increased expression of tissue inhibitors of metalloproteinase 3 (TIMP3).	Cetrimonium	0-4	TIMP metallopeptidase inhibitor 3	Homo sapiens	202-207
34558047-3	2022	In this work, the interaction quantitative model between resonance light scattering intensity and the concentration of binary surfactant mixtures NP-10+SDBS and NP-10+CTAB was established, and the mechanism of binary surfactant interaction was explored through the model by the resonance light scattering method.	Cetrimonium	167-171	nuclear receptor subfamily 4 group A member 1	Homo sapiens	146-151
34558047-3	2022	In this work, the interaction quantitative model between resonance light scattering intensity and the concentration of binary surfactant mixtures NP-10+SDBS and NP-10+CTAB was established, and the mechanism of binary surfactant interaction was explored through the model by the resonance light scattering method.	Cetrimonium	167-171	nuclear receptor subfamily 4 group A member 1	Homo sapiens	161-166
34848464-6	2021	In addition, CTAB reduced the phosphorylation of mothers against decapentaplegic homolog 2/3 (Smad2/3) proteins, which mediated CTAB-inhibited migration and invasion in SCC4 cells.	Cetrimonium	13-17	SMAD family member 2	Homo sapiens	94-101
34848464-8	2021	CONCLUSION: CTAB attenuates the mesenchymal characteristics through upregulation of TIMP3 by inhibiting the canonical TGF-beta/Smad/miR-181b/TIMP3 signaling involved in extracellular matrix remodeling in SCC4 cells and might be a promising anti-metastatic therapeutic agent for TSCC.	Cetrimonium	12-16	transforming growth factor alpha	Homo sapiens	118-126
34848464-6	2021	In addition, CTAB reduced the phosphorylation of mothers against decapentaplegic homolog 2/3 (Smad2/3) proteins, which mediated CTAB-inhibited migration and invasion in SCC4 cells.	Cetrimonium	128-132	SMAD family member 2	Homo sapiens	94-101
34848464-8	2021	CONCLUSION: CTAB attenuates the mesenchymal characteristics through upregulation of TIMP3 by inhibiting the canonical TGF-beta/Smad/miR-181b/TIMP3 signaling involved in extracellular matrix remodeling in SCC4 cells and might be a promising anti-metastatic therapeutic agent for TSCC.	Cetrimonium	12-16	TIMP metallopeptidase inhibitor 3	Homo sapiens	141-146
34217948-7	2021	The surface is negatively charged at pH 10 and pH 12, and sufficiently charged to attract cooperative adsorption of CTAB aggregates at pH 12.	Cetrimonium	116-120	phenylalanine hydroxylase	Homo sapiens	37-39
34217948-7	2021	The surface is negatively charged at pH 10 and pH 12, and sufficiently charged to attract cooperative adsorption of CTAB aggregates at pH 12.	Cetrimonium	116-120	phenylalanine hydroxylase	Homo sapiens	47-49
34217948-7	2021	The surface is negatively charged at pH 10 and pH 12, and sufficiently charged to attract cooperative adsorption of CTAB aggregates at pH 12.	Cetrimonium	116-120	phenylalanine hydroxylase	Homo sapiens	135-137
34281838-0	2021	Cetyltrimethylammonium Bromide Attenuates the Mesenchymal Characteristics of Hypopharyngeal Squamous Cell Carcinoma Through Inhibiting the EGFR/PI3K/AKT Signaling Pathway.	Cetrimonium	0-30	AKT serine/threonine kinase 1	Homo sapiens	149-152
34519933-4	2021	In this work, a new nanobiosensor based on the fluorescence property of r-GQD@HTAB (reduced graphene quantum dots modified with hexadecyl trimethyl ammonium bromide) was fabricated that can identify the SRY gene in cffDNA with high sensitivity and specificity.	Cetrimonium	128-164	sex determining region Y	Homo sapiens	203-206
34281838-9	2021	Further investigation showed that CTAB treatment suppressed the phosphorylation of extracellular-regulated kinase 1/2, mechanistic target of rapamycin kinase and AKT serine/threonine kinase 1.	Cetrimonium	34-38	AKT serine/threonine kinase 1	Homo sapiens	162-191
34281838-0	2021	Cetyltrimethylammonium Bromide Attenuates the Mesenchymal Characteristics of Hypopharyngeal Squamous Cell Carcinoma Through Inhibiting the EGFR/PI3K/AKT Signaling Pathway.	Cetrimonium	0-30	epidermal growth factor receptor	Homo sapiens	139-143
34281838-10	2021	CTAB also repressed the expression and phosphorylation levels of epidermal growth factor receptor (EGFR) and phosphatidylinositol-4,5-bisphosphate 3-kinase (PI3K), and the partial restoration of mesenchymal phenotype by EGF addition confirmed that CTAB inhibited migration and invasion in HPSCC cells by blocking the EGFR signaling pathway.	Cetrimonium	0-4	epidermal growth factor receptor	Homo sapiens	65-97
34281838-10	2021	CTAB also repressed the expression and phosphorylation levels of epidermal growth factor receptor (EGFR) and phosphatidylinositol-4,5-bisphosphate 3-kinase (PI3K), and the partial restoration of mesenchymal phenotype by EGF addition confirmed that CTAB inhibited migration and invasion in HPSCC cells by blocking the EGFR signaling pathway.	Cetrimonium	0-4	epidermal growth factor receptor	Homo sapiens	99-103
34281838-10	2021	CTAB also repressed the expression and phosphorylation levels of epidermal growth factor receptor (EGFR) and phosphatidylinositol-4,5-bisphosphate 3-kinase (PI3K), and the partial restoration of mesenchymal phenotype by EGF addition confirmed that CTAB inhibited migration and invasion in HPSCC cells by blocking the EGFR signaling pathway.	Cetrimonium	0-4	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta	Homo sapiens	109-155
34281838-10	2021	CTAB also repressed the expression and phosphorylation levels of epidermal growth factor receptor (EGFR) and phosphatidylinositol-4,5-bisphosphate 3-kinase (PI3K), and the partial restoration of mesenchymal phenotype by EGF addition confirmed that CTAB inhibited migration and invasion in HPSCC cells by blocking the EGFR signaling pathway.	Cetrimonium	0-4	epidermal growth factor receptor	Homo sapiens	317-321
34281838-10	2021	CTAB also repressed the expression and phosphorylation levels of epidermal growth factor receptor (EGFR) and phosphatidylinositol-4,5-bisphosphate 3-kinase (PI3K), and the partial restoration of mesenchymal phenotype by EGF addition confirmed that CTAB inhibited migration and invasion in HPSCC cells by blocking the EGFR signaling pathway.	Cetrimonium	248-252	epidermal growth factor receptor	Homo sapiens	317-321
34281838-11	2021	CONCLUSION: Our results suggest that CTAB is involved in the suppression of EGFR-mediated mesenchymal phenotype and the molecular mechanism by which CTAB obstructs HPSCC cell metastasis may represent a promising strategy for use in HPSCC treatment.	Cetrimonium	37-41	epidermal growth factor receptor	Homo sapiens	76-80
35452932-3	2022	In this study, polyethylene (PE) and polypropylene (PP) were evaluated for Pb(II) adsorption and desorption mechanism in the presence of two surfactants: cetyltrimethylammonium bromide (CTAB) and sodium dodecylbenzenesulfonate (SDBS).	Cetrimonium	154-184	submaxillary gland androgen regulated protein 3B	Homo sapiens	75-81
34361661-1	2021	Hierarchical MOR-type zeolites were synthesized in the presence of hexadecyltrimethylammonium bromide (CTAB) as a porogen agent.	Cetrimonium	67-101	opioid receptor mu 1	Homo sapiens	13-16
34361661-1	2021	Hierarchical MOR-type zeolites were synthesized in the presence of hexadecyltrimethylammonium bromide (CTAB) as a porogen agent.	Cetrimonium	103-107	opioid receptor mu 1	Homo sapiens	13-16
34361661-2	2021	XRD proved that the concentration of CTAB in the synthesis medium plays an essential role in forming pure hierarchical MOR-type material.	Cetrimonium	37-41	opioid receptor mu 1	Homo sapiens	119-122
34361661-7	2021	In addition, mesoporous volume and BET surface seem to increase upon the increase of CTAB concentration in the synthesis medium.	Cetrimonium	85-89	delta/notch like EGF repeat containing	Homo sapiens	35-38
35452932-3	2022	In this study, polyethylene (PE) and polypropylene (PP) were evaluated for Pb(II) adsorption and desorption mechanism in the presence of two surfactants: cetyltrimethylammonium bromide (CTAB) and sodium dodecylbenzenesulfonate (SDBS).	Cetrimonium	186-190	submaxillary gland androgen regulated protein 3B	Homo sapiens	75-81
35585299-2	2022	For this purpose, the porous MIP sensor was prepared using tetraethyl orthosilicate (TEOS) and cetyltrimethylammonium bromide (CTAB) in the presence of beta-cyclodextrin (beta-CD) as a chiral recognizing element on a glassy carbon electrode (GCE).	Cetrimonium	127-131	ACD shelterin complex subunit and telomerase recruitment factor	Homo sapiens	171-178
35390365-5	2022	Combined exposure to CTAB and BPA induced changes on the ER, Golgi apparatus, nucleoli and cytoplasmic RNA in one of the cell lines.	Cetrimonium	21-25	epiregulin	Homo sapiens	57-59
35424647-1	2022	A technique of obtaining plexitonic structures based on Ag2S quantum dots passivated with l-cysteine (Ag2S/l-Cys QDs) in the presence of Au nanorods passivated with cetyltrimethylammonium bromide molecules (Au/CTAB NRs) with controlled luminescence properties has been developed.	Cetrimonium	210-214	angiotensin II receptor type 1	Homo sapiens	102-106
35149242-5	2022	Briefly, poly (3-sulfopropyl methacrylate potassium salt) (PSPMA) brushes were constructed by surface-initiated atom transfer radical polymerization on silicon or cotton fabric substrates, and a positive-charged component, namely lysozyme (LYZ), hexadecyl trimethyl ammonium bromide (CTAB) or chitosan (CS), was loaded on negative-charged sulfonate groups through electrostatic interactions.	Cetrimonium	246-282	lysozyme	Homo sapiens	230-238
35149242-5	2022	Briefly, poly (3-sulfopropyl methacrylate potassium salt) (PSPMA) brushes were constructed by surface-initiated atom transfer radical polymerization on silicon or cotton fabric substrates, and a positive-charged component, namely lysozyme (LYZ), hexadecyl trimethyl ammonium bromide (CTAB) or chitosan (CS), was loaded on negative-charged sulfonate groups through electrostatic interactions.	Cetrimonium	284-288	lysozyme	Homo sapiens	230-238
35328470-5	2022	The largest stability was observed in the PAA-HMW/CTAB system.	Cetrimonium	50-54	cilia and flagella associated protein 97	Homo sapiens	46-49
35424647-2	2022	The structural and luminescence properties of Ag2S/l-Cys QDs with Au/CTAB NRs are studied.	Cetrimonium	69-73	angiotensin II receptor type 1	Homo sapiens	46-50
35424647-7	2022	With weak plexcitonic coupling in the nanostructures (Ag2S QD/l-Cys)/(polyDADMAC)/(Au/CTAB NRs), the possibility of increasing the quantum yield of trap state luminescence for Ag2S QDs due to the Purcell effect has been demonstrated.	Cetrimonium	86-90	angiotensin II receptor type 1	Homo sapiens	54-58
35424647-7	2022	With weak plexcitonic coupling in the nanostructures (Ag2S QD/l-Cys)/(polyDADMAC)/(Au/CTAB NRs), the possibility of increasing the quantum yield of trap state luminescence for Ag2S QDs due to the Purcell effect has been demonstrated.	Cetrimonium	86-90	angiotensin II receptor type 1	Homo sapiens	176-180
35424647-8	2022	In the case of formation (Ag2S QD/l-Cys)/(polyDADMAC)/(Au/CTAB NRs) a transformation of shallow trap state structure was established using the thermostimulated luminescence method.	Cetrimonium	58-62	angiotensin II receptor type 1	Homo sapiens	26-30
35209443-1	2022	The luminescence properties of Ag2S quantum dots passivated with L-Cysteine (Ag2S/L-Cys QDs) are studied in the presence of Au nanorods passivated with cetyltrimethylammonium bromide molecules (Au/CTAB NRs).	Cetrimonium	197-201	angiotensin II receptor type 1	Homo sapiens	77-81
35209443-6	2022	With weak plexcitonic coupling in the nanostructures (Ag2S QD/L-Cys)/(PolyDADMAC)/(Au/CTAB NRs), the possibility of increasing the quantum yield of trap state luminescence for Ag2S QDs due to the Purcell effect has been demonstrated.	Cetrimonium	86-90	angiotensin II receptor type 1	Homo sapiens	54-58
35209443-6	2022	With weak plexcitonic coupling in the nanostructures (Ag2S QD/L-Cys)/(PolyDADMAC)/(Au/CTAB NRs), the possibility of increasing the quantum yield of trap state luminescence for Ag2S QDs due to the Purcell effect has been demonstrated.	Cetrimonium	86-90	angiotensin II receptor type 1	Homo sapiens	176-180