PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
30544045-3	2019	The biosurfactant obtained with these selected strains showed the capacity of decreasing the surface tension of water from 72.0 to 31.8 mN.m-1 and the interfacial tension of n-hexadecane to 27.2 mN.m-1, with a critical micelle concentration of 12.5 mg.L-1.	n-hexadecane	174-186	L1 cell adhesion molecule	Mus musculus	252-255
31336240-4	2019	Compared to that of SCS, SMA-SCS exhibited better adsorption performance with maximum adsorption capacities of 0.23 and 0.28 mg/g for hexadecane and rhamnolipid, respectively.	n-hexadecane	134-144	survival of motor neuron 1, telomeric	Homo sapiens	25-28
31336240-6	2019	Up to 81.1% of hexadecane removal was achieved over 20 g/L of SMA-SCS within 24 h, whereas only 36% of rhamnolipid was degraded.	n-hexadecane	15-25	survival of motor neuron 1, telomeric	Homo sapiens	62-65
32503904-3	2020	The expression of ssuD and tauD occurred under sulfate-limited conditions generated during n-hexadecane degradation.	n-hexadecane	91-103	taurine dioxygenase	Acinetobacter oleivorans DR1	27-31
32503904-8	2020	Removal of this byproduct by SsuD and TauD must be necessary for bacterial survival under oxidative stress generated during n-hexadecane degradation.	n-hexadecane	124-136	taurine dioxygenase	Acinetobacter oleivorans DR1	38-42
32328734-3	2020	During growth on hexadecane as sole carbon source, the activity of 3-hydroxyacyl-CoA dehydrogenase, a beta-oxidation pathway enzyme, was measured.	n-hexadecane	17-27	succinate-CoA ligase ADP-forming subunit beta	Homo sapiens	100-106
31336240-2	2019	In this work, the removal of rhamnolipid-solubilized hexadecane via a salicylic acid-methanol-acetone modified steel converter slag (SMA-SCS) catalyzed Fenton-like process was studied.	n-hexadecane	53-63	survival of motor neuron 1, telomeric	Homo sapiens	133-136
31591464-9	2019	Oxalate production during hexadecane degradation and impaired growth of a DeltaldhDeltaglcB double mutant in both acetate and hexadecane-supplemented media suggested that LDH is a potential detoxifying enzyme for glyoxylate.	n-hexadecane	26-36	D-lactate dehydrogenase	Acinetobacter oleivorans DR1	171-174
31591464-9	2019	Oxalate production during hexadecane degradation and impaired growth of a DeltaldhDeltaglcB double mutant in both acetate and hexadecane-supplemented media suggested that LDH is a potential detoxifying enzyme for glyoxylate.	n-hexadecane	126-136	D-lactate dehydrogenase	Acinetobacter oleivorans DR1	171-174
22917079-9	2012	Elevated levels of IL-1alpha were also found in supernatants of cells treated with pristane and hexadecane.	n-hexadecane	96-106	interleukin 1 alpha	Rattus norvegicus	19-28
30460831-9	2018	At the concentrations of 100 mug mL-1, 200 mug mL-1, compound tetradecane and hexadecane were more attractive to the larvae than the control.	n-hexadecane	78-88	L1 cell adhesion molecule	Mus musculus	33-37
30460831-9	2018	At the concentrations of 100 mug mL-1, 200 mug mL-1, compound tetradecane and hexadecane were more attractive to the larvae than the control.	n-hexadecane	78-88	L1 cell adhesion molecule	Mus musculus	47-51
28315676-4	2017	With the use of a panel of MHC-III recombinant inbred strains, we found that the 33-kb Ltab-Ncr3 haplotype in MHC-III was linked to the induction of arthritis with incomplete Freund"s adjuvant, with similar effects in arthritis induced by several oil adjuvants (hexadecane, heptadecane, squalene, arlacel).	n-hexadecane	262-272	natural cytotoxicity triggering receptor 3	Homo sapiens	92-96
25956940-6	2015	Red clay also upregulated genes related to oxidative stress defense, such as superoxide dismutase, catalase, and glutaredoxin genes, suggesting that red clay supports the response of DR1 cells to oxidative stress generated during hexadecane utilization.	n-hexadecane	230-240	catalase family protein	Acinetobacter oleivorans DR1	99-107
25956940-6	2015	Red clay also upregulated genes related to oxidative stress defense, such as superoxide dismutase, catalase, and glutaredoxin genes, suggesting that red clay supports the response of DR1 cells to oxidative stress generated during hexadecane utilization.	n-hexadecane	230-240	glutaredoxin 3	Acinetobacter oleivorans DR1	113-125
25875917-3	2015	Neutron reflectivity was used with a carefully selected set of isotopic contrasts to study the adsorption of bovine serum albumin (BSA) at the hexadecane/water interface, and the results were compared to those for the air/water interface.	n-hexadecane	143-153	albumin	Homo sapiens	116-129
25169952-1	2014	In this study, we demonstrate that while the energy density and lubricity of the C15 and C16 products of furan condensation of biomass-derived aldehydes with 2-methylfuran are consistent with requirements for diesel, these products do not meet specifications for cetane number and pour point due to their aromatic furan rings.	n-hexadecane	263-269	placenta associated 8	Homo sapiens	81-84
24752075-1	2014	The alcohol oxidase (AOx) cDNA from Aspergillus terreus MTCC6324 with an open reading frame (ORF) of 2001 bp was constructed from n-hexadecane induced cells and expressed in Escherichia coli with a yield of ~4.2 mg protein g-1 wet cell.	n-hexadecane	130-142	acyl-CoA oxidase 1	Rattus norvegicus	21-24
24458564-5	2014	Batch culture of G. ajoucoccus A2(T) in a bioreactor containing 1 % (v/v) hexadecane or 1 % (v/v) commercial diesel yielded 25 mg L-1 and 2.6 mg L-1 of carotenoids, respectively.	n-hexadecane	74-84	L1 cell adhesion molecule	Homo sapiens	130-139
24224524-2	2013	We also demonstrate the effects of varying the concentration of the SFN sol on the water and hexadecane repellency and on the transparency of the coated glass substrates.	n-hexadecane	93-103	RNA exonuclease 2	Homo sapiens	68-71
22833369-7	2013	A proof-of-principle experiment for the one-pot bio-ester production from glucose led to 5 g L(-1) butyl butyrate in the hexadecane phase.	n-hexadecane	121-131	immunoglobulin kappa variable 1-16	Homo sapiens	93-98
21768743-2	2011	Three proteins, bovine serum albumin (BSA), beta-lactoglobulin (beta-lg), and beta-casein (beta-ca), were employed to disperse hexadecane in various pH and ionic strength solutions in a wide range of oil-water ratios.	n-hexadecane	127-137	casein beta	Homo sapiens	78-89
21768743-2	2011	Three proteins, bovine serum albumin (BSA), beta-lactoglobulin (beta-lg), and beta-casein (beta-ca), were employed to disperse hexadecane in various pH and ionic strength solutions in a wide range of oil-water ratios.	n-hexadecane	127-137	casein beta	Homo sapiens	78-85
19114507-6	2009	The identification of these metabolites suggests a carbon addition at the C-3 position of hexadecane, with subsequent beta-oxidation and transformation reactions (chain elongation and C-10 methylation) that predominantly produce fatty acids with odd numbers of carbons.	n-hexadecane	90-100	homeobox C10	Homo sapiens	184-188
20428538-1	2010	Ellipsometry was employed to study the adsorption to the hexadecane-water interface of the simple non-ionic hydrocarbon surfactant C(10)E(8) and the two milk proteins beta-casein and beta-lactoglobulin, as well as the competitive adsorption of each protein with the surfactant.	n-hexadecane	57-67	casein beta	Homo sapiens	167-178
16309812-11	2006	n-Hexadecane induced hypergammaglobulinemia (IgG1, IgG2a), antinuclear (titer>1:160, 67%) and -cytoplasmic antibodies (58%) and autoantibodies to nRNP/Sm (25%), Su (33%), ssDNA (83%), and chromatin (100%).	n-hexadecane	0-12	LOC105243590	Mus musculus	45-49
19174897-1	2008	The SPARC vapor pressure and activity coefficient models were coupled to successfully estimate Henry"s Law Constant (HLC) in water and in hexadecane for a wide range of organic compounds without modification to, or additional parametrization of, either SPARC model.	n-hexadecane	138-148	secreted protein acidic and cysteine rich	Homo sapiens	4-9
18715079-7	2008	The encounter rate constants appear to be dominated by hydrodynamic forces, forming a common curve for hexane, decane, and hexadecane when plotted against T/eta, where eta is the shear viscosity.	n-hexadecane	123-133	endothelin receptor type A	Homo sapiens	157-160
18715079-7	2008	The encounter rate constants appear to be dominated by hydrodynamic forces, forming a common curve for hexane, decane, and hexadecane when plotted against T/eta, where eta is the shear viscosity.	n-hexadecane	123-133	endothelin receptor type A	Homo sapiens	168-171
18240147-5	2008	Extensive (including both Mp and Eh) and partial (either Mp or Eh) MGMT methylation were found in 24.5% and 11.6% of CRCs, 3.8% and 27.9% of APs, 0.5% and 7.7% of C-Ns and 2.8% and 2.8% of N-Ns, respectively.	n-hexadecane	163-167	O-6-methylguanine-DNA methyltransferase	Homo sapiens	67-71
17454365-1	2007	Chloronaphthalenes (CNs), due to their structural similarities to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and the other "dioxin-like" compounds, can bind to the aryl hydrocarbon receptor (AhR) and induce a wide range of pleotrophic effects.	n-hexadecane	20-23	aryl hydrocarbon receptor	Rattus norvegicus	164-189
17454365-1	2007	Chloronaphthalenes (CNs), due to their structural similarities to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and the other "dioxin-like" compounds, can bind to the aryl hydrocarbon receptor (AhR) and induce a wide range of pleotrophic effects.	n-hexadecane	20-23	aryl hydrocarbon receptor	Rattus norvegicus	191-194
16917538-7	2006	The presence of hexadecane negatively affected these activities and lowered the amounts of exopolysaccharides in CNP and P biofilms in fall 1999 but increased the biofilm activities and exopolysaccharide amounts in CNP biofilm in fall 2001.	n-hexadecane	16-26	2',3'-cyclic nucleotide 3' phosphodiesterase	Homo sapiens	113-116
16917538-7	2006	The presence of hexadecane negatively affected these activities and lowered the amounts of exopolysaccharides in CNP and P biofilms in fall 1999 but increased the biofilm activities and exopolysaccharide amounts in CNP biofilm in fall 2001.	n-hexadecane	16-26	2',3'-cyclic nucleotide 3' phosphodiesterase	Homo sapiens	215-218
16485121-8	2006	In an all ALI environment, no single hydrocarbon is the dominating factor in the determination of HEK cytotoxicity while deletion of hexadecane resulted in a 2.5-fold increase in IL-8 production.	n-hexadecane	133-143	C-X-C motif chemokine ligand 8	Homo sapiens	179-183
16309812-11	2006	n-Hexadecane induced hypergammaglobulinemia (IgG1, IgG2a), antinuclear (titer>1:160, 67%) and -cytoplasmic antibodies (58%) and autoantibodies to nRNP/Sm (25%), Su (33%), ssDNA (83%), and chromatin (100%).	n-hexadecane	0-12	immunoglobulin heavy variable V1-9	Mus musculus	51-56
11510537-1	2001	Experimental methods based on gas-phase chromatography were tested with a view to determine the gas-liquid n-hexadecane partition coefficients, log L16 of non-volatile compounds at 298.2 K. It was demonstrated that reliable values of log L16 of compounds more volatile than n-docosane can be obtained using either capillary, or packed columns.	n-hexadecane	107-119	immunoglobulin kappa variable 3D-15	Homo sapiens	238-241
15784000-1	2005	Crystallization of n-hexadecane in emulsion droplets was studied using time-resolved two-dimensional small- and wide-angle x-ray scattering with differential scanning calorimetry (2D-SAXS-WAXS-in situ DSC) which provides information about both nano- and subnanoscale structural change.	n-hexadecane	19-31	desmocollin 3	Homo sapiens	201-204
11513424-3	2001	The software allows the determination of PAH emissions as a function of the fuel composition parameters (aromatic content, cetane index, gross heat power, nitrogen and sulphur content) and operation conditions (torque and engine speed).	n-hexadecane	123-129	phenylalanine hydroxylase	Homo sapiens	41-44
11133096-3	2000	Hexadecane- and dodecanesulfonyl fluorides caused 50% inhibition of LPL activity at concentrations of 10 to 20 microM.	n-hexadecane	0-10	lipoprotein lipase	Homo sapiens	68-71
10446711-6	1999	Strain DB1 grew on benzoate, dibenzothiophene sulfone, and hexadecanoic acid, but it could not grow on benzofuran, dibenzothiophene, dibenzothiophene sulfoxide, hexadecane, indole, naphthalene, phenol, 2-sulfobenzoic acid, sulfolane, benzothiophene, or 3- or 5-methylbenzothiophenes.	n-hexadecane	161-171	vascular endothelial zinc finger 1	Homo sapiens	7-10
11088429-1	2000	Thin (thickness h approximately 3 nm) films of n-octadecane and n-hexadecane adsorbed on mica surfaces from vapor close to their bulk melting points (T(m)) have been studied in a surface force apparatus.	n-hexadecane	64-76	MHC class I polypeptide-related sequence A	Homo sapiens	89-93
10795574-1	2000	Bovine beta-Lactoglobulin (BLG) was cleaved by BNPS-skatole (2-(2"-nitrophenylsulfenyl)-3-methyl-3"-bromoindolenine), trypsin, or pepsin in 40% ethanol before emulsification with hexadecane in order to characterize the peptides active at the interfaces.	n-hexadecane	179-189	beta-lactoglobulin	Bos taurus	7-25
10795574-1	2000	Bovine beta-Lactoglobulin (BLG) was cleaved by BNPS-skatole (2-(2"-nitrophenylsulfenyl)-3-methyl-3"-bromoindolenine), trypsin, or pepsin in 40% ethanol before emulsification with hexadecane in order to characterize the peptides active at the interfaces.	n-hexadecane	179-189	beta-lactoglobulin	Bos taurus	27-30
10959955-7	2000	The increased wetting of the C18 interphase in the order water < methanol < acetonitrile < tetrahydrofuran agreed with data for the miscibility of these solvents with n-hexadecane.	n-hexadecane	176-188	Bardet-Biedl syndrome 9	Homo sapiens	29-32
8954705-0	1996	Atomic Force Microscopy of Interfacial Protein Films Atomic force microscopy (AFM) has been used to image interfacial films of bovine serum albumen and beta-casein produced at hexadecane/water and air/water interfaces, respectively.	n-hexadecane	176-186	casein beta	Homo sapiens	152-163
9500987-7	1998	CYP86A1 was found to catalyze the omega-hydroxylation of saturated and unsaturated fatty acids with chain lengths from C12 to C18 but not of hexadecane.	n-hexadecane	141-151	cytochrome P450, family 86, subfamily A, polypeptide 1	Arabidopsis thaliana	0-7
1519415-7	1992	Treatment of the bacteria by guanidinium chloride or by neuraminidase enhanced the hexadecane adherence.	n-hexadecane	83-93	neuraminidase 1	Homo sapiens	56-69
8924591-10	1996	Cetane number and upper distillation curve points were negatively correlated with both mutagenicity and Ah receptor affinity.	n-hexadecane	0-6	aryl hydrocarbon receptor	Homo sapiens	104-115
8987500-1	1995	A novel type of succinoyl trehalose lipid (STL-1) prepared from n-hexadecane-culture of Rhodococcus erythropolis SD-74 markedly inhibited the growth of a human monocytoid leukemic cell line, U937, and induced its morphological alteration along a monocyte-macrophage lineage.	n-hexadecane	64-76	collagen type II alpha 1 chain	Homo sapiens	43-48
1457045-6	1992	Three of the five additional CYP52 genes could be successfully expressed in Saccharomyces cerevisiae and display different substrate specificities in in vitro assays with model substrates: alk2 and alk3 exhibit a strong preference for hexadecane, while alk4 and alk5 preferentially hydroxylate lauric acid.	n-hexadecane	235-245	protein kinase ALK2	Saccharomyces cerevisiae S288C	189-193
7884677-4	1994	The slopes of plots of log PRX vs log KRX were 0.85, 0.91, 0.99, and 2.4, respectively, for hexadecane/water, hexadecene/water, 1,9-decadiene/water, and octanol/water with the best model solvent being that which yielded a slope closest to unity.	n-hexadecane	92-102	periaxin	Homo sapiens	27-30
34271488-9	2021	16.6  C which is significantly lower than the melting temperature of crystalline hexadecane, 18  C. The scattering results are in a very good agreement with the complementary optical observations and DSC measurements.	n-hexadecane	81-91	desmocollin 3	Homo sapiens	200-203
34921957-2	2022	The affinity to hexadecane was significantly increased in STWT, STKCCM, and STCCARM cells after P22 infection.	n-hexadecane	16-26	calcineurin like EF-hand protein 1	Homo sapiens	96-99
1937041-8	1991	Upon expression of CYP52A2 in Saccharomyces cerevisiae, alk2 was shown to hydroxylate hexadecane, but had no hydroxylation activity towards lauric acid, whereas alk1 showed both activities.	n-hexadecane	86-96	protein kinase ALK2	Saccharomyces cerevisiae S288C	56-60
3880729-0	1985	Human plasma fibronectin inhibits adherence of Streptococcus pyogenes to hexadecane.	n-hexadecane	73-83	fibronectin 1	Homo sapiens	13-24
2578811-2	1985	However, for the ATPase reconstituted into bilayers of dimyristoleoylphosphatidylcholine, a pattern of activation at low concentration followed by inhibition at higher concentration is seen for hexachlorocyclohexanes and alkanes such as decane and hexadecane.	n-hexadecane	248-258	dynein axonemal heavy chain 8	Homo sapiens	17-23
2545200-0	1989	Effect of hexadecane on piglet epidermal ornithine decarboxylase activity.	n-hexadecane	10-20	ornithine decarboxylase 1	Homo sapiens	41-64
2545200-2	1989	The application of hexadecane to epidermis from the backs of piglets less than 1 week old resulted in a rapid biphasic-rise in the level of ornithine decarboxylase (ODC) activity.	n-hexadecane	19-29	ornithine decarboxylase 1	Homo sapiens	140-163
2545200-2	1989	The application of hexadecane to epidermis from the backs of piglets less than 1 week old resulted in a rapid biphasic-rise in the level of ornithine decarboxylase (ODC) activity.	n-hexadecane	19-29	ornithine decarboxylase 1	Homo sapiens	165-168
2545200-5	1989	The activation of this latent ODC by hexadecane was independent of extracellular calcium.	n-hexadecane	37-47	ornithine decarboxylase 1	Homo sapiens	30-33
3272747-3	1988	ODC activity and polyamine levels (putrescine, spermidine and spermine) in the epidermis were significantly increased and reached maximum elevations at 12 h after the start of n-hexadecane treatment with DNA synthesis peaking at 24 h. Histological studies confirmed a significant cellular edema at 24 h after the beginning of the treatment followed at 48 h by an epidermal hyperplasia which was maximum at 72 h. These data support the view that ODC activation, increased biosynthesis of polyamines and DNA are early events in epidermal cell hyperproliferation.	n-hexadecane	176-188	ornithine decarboxylase 1	Rattus norvegicus	0-3
3272747-3	1988	ODC activity and polyamine levels (putrescine, spermidine and spermine) in the epidermis were significantly increased and reached maximum elevations at 12 h after the start of n-hexadecane treatment with DNA synthesis peaking at 24 h. Histological studies confirmed a significant cellular edema at 24 h after the beginning of the treatment followed at 48 h by an epidermal hyperplasia which was maximum at 72 h. These data support the view that ODC activation, increased biosynthesis of polyamines and DNA are early events in epidermal cell hyperproliferation.	n-hexadecane	176-188	ornithine decarboxylase 1	Rattus norvegicus	445-448
4036272-9	1985	Addition of bovine serum albumin (BSA) antigen to the oil phase of 5% hexadecane emulsions tended to destabilize the emulsions, especially at higher protein concentrations.	n-hexadecane	70-80	albumin	Mus musculus	19-46
3880729-1	1985	The effect of human plasma fibronectin on the adherence of Streptococcus pyogenes to hexadecane droplets was investigated.	n-hexadecane	85-95	fibronectin 1	Homo sapiens	27-38
3880729-2	1985	Fibronectin blocked the adherence of streptococci to hexadecane in a dose-dependent manner.	n-hexadecane	53-63	fibronectin 1	Homo sapiens	0-11
3880729-4	1985	Chemical treatments of streptococci that decreased streptococcal binding of fibronectin also decreased their binding to hexadecane.	n-hexadecane	120-130	fibronectin 1	Homo sapiens	76-87
3880729-5	1985	Pretreatment of fibronectin with lipoteichoic acid blocked the binding of fibronectin to streptococci and abolished its ability to inhibit streptococcal adherence to hexadecane in a dose-related manner.	n-hexadecane	166-176	fibronectin 1	Homo sapiens	16-27
3880729-5	1985	Pretreatment of fibronectin with lipoteichoic acid blocked the binding of fibronectin to streptococci and abolished its ability to inhibit streptococcal adherence to hexadecane in a dose-related manner.	n-hexadecane	166-176	fibronectin 1	Homo sapiens	74-85
3880729-7	1985	The data suggest that fibronectin binds to lipoteichoic acid on the surface of the streptococci, thereby preventing lipoteichoic acid from interacting with the hexadecane phase.	n-hexadecane	160-170	fibronectin 1	Homo sapiens	22-33
6688940-8	1983	As a consequence of the solubilization of the emulsan capsule, RAG-1 cells became more hydrophobic, as determined by adherence to hexadecane.	n-hexadecane	130-140	hexose transporter HXT4	Saccharomyces cerevisiae S288C	63-68
6546308-3	1984	However, binding of phage ap3 occurred at the interfaces of hexadecane-in-water emulsions specifically stabilized by emulsan polymers.	n-hexadecane	60-70	adaptor-related protein complex 3, beta 1 subunit	Mus musculus	26-29
30025-5	1978	ADH bound to the cell structures dehydrated mainly C5--C16 alcohols; the activity of these ADH was almost by an order of magnitude higher in the "hexadecane cells" as compared to the "glucose cells" (in contrast to soluble ADH).	n-hexadecane	146-156	alcohol dehydrogenase 1A (class I), alpha polypeptide	Homo sapiens	0-3
7263064-0	1981	Adherence of Acinetobacter calcoaceticus RAG-1 to human epithelial cells and to hexadecane.	n-hexadecane	80-90	recombination activating 1	Homo sapiens	41-46
7263064-2	1981	RAG-1, a microorganism originally isolated for growth on hydrocarbon, adhered to epithelial cells when grown under conditions which promote its adherence to hexadecane; similarly, RAG-1 cells adhered poorly to epithelial cells when grown under conditions which cause the cells to possess low affinity towards hexadecane.	n-hexadecane	157-167	recombination activating 1	Homo sapiens	0-5
7263064-2	1981	RAG-1, a microorganism originally isolated for growth on hydrocarbon, adhered to epithelial cells when grown under conditions which promote its adherence to hexadecane; similarly, RAG-1 cells adhered poorly to epithelial cells when grown under conditions which cause the cells to possess low affinity towards hexadecane.	n-hexadecane	309-319	recombination activating 1	Homo sapiens	0-5
6766934-4	1980	Although another cytochrome P-450 fraction was active for hexadecane hydroxylation, this fraction had little activity.	n-hexadecane	58-68	cytochrome P-450	Oryctolagus cuniculus	17-33
205235-4	1978	The concentration of skin cyclic AMP fell immediately after hexadecane application and subsequently rose to give a prolonged increase.	n-hexadecane	60-70	transmembrane serine protease 5	Rattus norvegicus	33-36
205235-5	1978	Use of the combined topical application of hexadecane and the anti-inflammatory drugs triamcinolone acetonide, hydrocortisone and indomethacin showed that the hexadecane-induced changes in DNA synthesis and glycogen metabolism were linked to the initial fall in cyclic AMP concentration.	n-hexadecane	159-169	transmembrane serine protease 5	Rattus norvegicus	269-272
135754-4	1976	Four enzymes that may be involved in glucose metabolism, hexokinase, glucose-6-phosphate dehydrogenase, glucose-phosphate isomerase, and succinate dehydrogenase, were not detected in cells grown on hexadecane but were present in cells grown on glucose.	n-hexadecane	198-208	hexokinase 1	Homo sapiens	57-67
135754-6	1976	Cells grown on hexadecane and transferred to glucose metabolize intracellular hexadecane; after 1 day, activity of hexokinase, glucose-6-phosphate dehydrogenase, glucosephosphate isomerase, and succinate dehydrogenase could be detected and 22% of the intracellular hydrocarbon had been metabolized.	n-hexadecane	15-25	hexokinase 1	Homo sapiens	115-125
135754-6	1976	Cells grown on hexadecane and transferred to glucose metabolize intracellular hexadecane; after 1 day, activity of hexokinase, glucose-6-phosphate dehydrogenase, glucosephosphate isomerase, and succinate dehydrogenase could be detected and 22% of the intracellular hydrocarbon had been metabolized.	n-hexadecane	78-88	hexokinase 1	Homo sapiens	115-125
7287656-8	1981	Hexadecane hydroxylation activity was solubilized from the intestinal microsomes and reconstituted with a partially purified cytochrome P-450 fraction, and intestinal NADPH-cytochrome c reductase, or spinach ferredoxin and ferredoxin-NADP reductase.	n-hexadecane	0-10	cytochrome P-450	Oryctolagus cuniculus	125-141
7287656-9	1981	The chromatography of the crude cytochrome P-450 preparation on hydroxylapatite separated at least two cytochrome P-450 fractions; one preferentially hydroxylating hexadecane, and the other preferentially hydroxylating myristic acid.	n-hexadecane	164-174	cytochrome P-450	Oryctolagus cuniculus	32-48
7287656-9	1981	The chromatography of the crude cytochrome P-450 preparation on hydroxylapatite separated at least two cytochrome P-450 fractions; one preferentially hydroxylating hexadecane, and the other preferentially hydroxylating myristic acid.	n-hexadecane	164-174	cytochrome P-450	Oryctolagus cuniculus	103-119
7287656-10	1981	The results suggest that rabbit intestinal mucosa microsomes had a cytochrome P-450 species specialized for hexadecane hydroxylation.	n-hexadecane	108-118	cytochrome P-450	Oryctolagus cuniculus	67-83
30025-6	1978	The character of changes in the activity of ADH toward various alcohols in the course of physiological adaptation of the yeast to oxidation of glucose and hexadecane suggests that both soluble and bound ADH contain at least two ADH, one of which is specific to lower alcohols and the other to higher alcohols.	n-hexadecane	155-165	alcohol dehydrogenase 1A (class I), alpha polypeptide	Homo sapiens	44-47
30025-6	1978	The character of changes in the activity of ADH toward various alcohols in the course of physiological adaptation of the yeast to oxidation of glucose and hexadecane suggests that both soluble and bound ADH contain at least two ADH, one of which is specific to lower alcohols and the other to higher alcohols.	n-hexadecane	155-165	alcohol dehydrogenase 1A (class I), alpha polypeptide	Homo sapiens	203-206
30025-6	1978	The character of changes in the activity of ADH toward various alcohols in the course of physiological adaptation of the yeast to oxidation of glucose and hexadecane suggests that both soluble and bound ADH contain at least two ADH, one of which is specific to lower alcohols and the other to higher alcohols.	n-hexadecane	155-165	alcohol dehydrogenase 1A (class I), alpha polypeptide	Homo sapiens	203-206
30025-5	1978	ADH bound to the cell structures dehydrated mainly C5--C16 alcohols; the activity of these ADH was almost by an order of magnitude higher in the "hexadecane cells" as compared to the "glucose cells" (in contrast to soluble ADH).	n-hexadecane	146-156	alcohol dehydrogenase 1A (class I), alpha polypeptide	Homo sapiens	91-94
30025-5	1978	ADH bound to the cell structures dehydrated mainly C5--C16 alcohols; the activity of these ADH was almost by an order of magnitude higher in the "hexadecane cells" as compared to the "glucose cells" (in contrast to soluble ADH).	n-hexadecane	146-156	alcohol dehydrogenase 1A (class I), alpha polypeptide	Homo sapiens	91-94
1160650-5	1975	The cells grown on the medium with hexadecane contain mycolic acids C32--C36, with C34- and C36-compounds prevailing and the aliphatic chain in alpha-position containing 10, 11, 12, and 14 C-atoms.	n-hexadecane	35-45	chemokine like factor	Homo sapiens	68-71
4136627-0	1974	Detection of cytochrome P-450 in subcellular fractions of Endomycopsislipolytica grown on n-hexadecane.	n-hexadecane	90-102	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	13-29
4562475-13	1972	Similarly, the supernatant obtained following growth of RAG-1 on hexadecane was capable of emulsifying crude oil in 60 min.	n-hexadecane	65-75	recombination activating 1	Homo sapiens	56-61
33006101-13	2021	This is mainly due to higher energy content and cetane number of DEE.	n-hexadecane	48-54	distal enhancer element	Homo sapiens	65-68
33231222-2	2020	Herein, we present a novel ionic beta-CD derivative that shows significant surface activity and stabilizes oil-in-water emulsions prepared with hexadecane as a model oil.	n-hexadecane	144-154	ACD shelterin complex subunit and telomerase recruitment factor	Homo sapiens	33-40