PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
1453273-4	1992	In addition, the trans-syn and cis-syn cyclobutane dimers of dCpT were obtained by acetophenone photosensitization and characterized.	acetophenone	83-95	synemin	Homo sapiens	23-26
8387596-2	1993	A series of progestin 16 alpha, 17 alpha-dioxolane ketals of acetophenone or substituted acetophenones that bind to the progesterone receptor (PgR) with comparable or higher affinities than the natural ligand, progesterone, have been prepared and evaluated as potential in vitro and in vivo probes for the progesterone receptor.	acetophenone	61-73	progesterone receptor	Homo sapiens	120-141
8387596-2	1993	A series of progestin 16 alpha, 17 alpha-dioxolane ketals of acetophenone or substituted acetophenones that bind to the progesterone receptor (PgR) with comparable or higher affinities than the natural ligand, progesterone, have been prepared and evaluated as potential in vitro and in vivo probes for the progesterone receptor.	acetophenone	61-73	progesterone receptor	Homo sapiens	143-146
1453273-4	1992	In addition, the trans-syn and cis-syn cyclobutane dimers of dCpT were obtained by acetophenone photosensitization and characterized.	acetophenone	83-95	synemin	Homo sapiens	35-38
1610807-3	1992	The insertion of a methylene bridge between the phenyl and tetrahydropyridine moieties of MPTP to yield N-methyl-4-benzyl-1,2,3,6-tetrahydropyridine, rendering the molecule more flexible, greatly enhances reactivity with MAO B, but not with MAO A, as compared with MPTP itself, in accord with data in the literature (Youngster et al., 1989a).	acetophenone	48-54	monoamine oxidase B	Homo sapiens	221-226
1610807-3	1992	The insertion of a methylene bridge between the phenyl and tetrahydropyridine moieties of MPTP to yield N-methyl-4-benzyl-1,2,3,6-tetrahydropyridine, rendering the molecule more flexible, greatly enhances reactivity with MAO B, but not with MAO A, as compared with MPTP itself, in accord with data in the literature (Youngster et al., 1989a).	acetophenone	48-54	monoamine oxidase A	Homo sapiens	241-246
34450988-8	2021	Three target gases, phenethyl alcohol, acetophenone and anethole, were perfectly discriminated, as the characteristic variables in the response matrix constructed by the combination of gas responses obtained 3 one-layer and 3 two-layer film-coated sensors.	acetophenone	39-51	gastrin	Homo sapiens	185-188
34111638-4	2021	We hypothesized that studied rhodococcal isolates, besides the regular one, use at least two alternative pathways for PCB transformation, including the pathway leading to acetophenone formation (via 3,4 (4,5) dioxygenase attack on the molecule), and a third sideway pathway that includes stepwise oxidative decarboxylation of the aliphatic side chain of the 2-hydroxy-6-oxo-6-phenylhexa-2,4-dienoate.	acetophenone	171-183	pyruvate carboxylase	Homo sapiens	118-121
1315745-1	1992	Recombinant cytochrome c peroxidase (CcP) and a W51A mutant of CcP, in contrast to other classical peroxidases, react with phenylhydrazine to give sigma-bonded phenyl-iron complexes.	acetophenone	123-129	cytochrome c, somatic	Homo sapiens	12-24
1991108-5	1991	The mechanism of the observed changes in thrombin affinity may involve a reduction in the pK of the hydroxyl group of tyrosine due to substitution of the electrophilic iodo or nitro group on the phenyl ring, resulting in an increased negative charge at neutral pH.	acetophenone	195-201	coagulation factor II, thrombin	Homo sapiens	41-49
2709330-7	1989	Therefore, the phenyl substitution appears to increase greatly the selectivity of the compound for AChE.	acetophenone	15-21	acetylcholinesterase (Cartwright blood group)	Homo sapiens	99-103
35276362-4	2022	Competitive binding assay of estrogen receptors ERalpha and ERbeta showed that diethanolamine derivative of 4-trifluoromethyl phenyl derivative 30 displayed 77.5-fold strong binding affinity towards ERalpha (IC50 = 0.004 muM) as compared to ERbeta (IC50 = 0.31 muM).	acetophenone	126-132	epiregulin	Homo sapiens	29-47
35276362-4	2022	Competitive binding assay of estrogen receptors ERalpha and ERbeta showed that diethanolamine derivative of 4-trifluoromethyl phenyl derivative 30 displayed 77.5-fold strong binding affinity towards ERalpha (IC50 = 0.004 muM) as compared to ERbeta (IC50 = 0.31 muM).	acetophenone	126-132	estrogen receptor 1	Homo sapiens	48-55
35276362-4	2022	Competitive binding assay of estrogen receptors ERalpha and ERbeta showed that diethanolamine derivative of 4-trifluoromethyl phenyl derivative 30 displayed 77.5-fold strong binding affinity towards ERalpha (IC50 = 0.004 muM) as compared to ERbeta (IC50 = 0.31 muM).	acetophenone	126-132	estrogen receptor 1	Homo sapiens	60-66
35276362-4	2022	Competitive binding assay of estrogen receptors ERalpha and ERbeta showed that diethanolamine derivative of 4-trifluoromethyl phenyl derivative 30 displayed 77.5-fold strong binding affinity towards ERalpha (IC50 = 0.004 muM) as compared to ERbeta (IC50 = 0.31 muM).	acetophenone	126-132	estrogen receptor 1	Homo sapiens	199-206
35276362-4	2022	Competitive binding assay of estrogen receptors ERalpha and ERbeta showed that diethanolamine derivative of 4-trifluoromethyl phenyl derivative 30 displayed 77.5-fold strong binding affinity towards ERalpha (IC50 = 0.004 muM) as compared to ERbeta (IC50 = 0.31 muM).	acetophenone	126-132	estrogen receptor 1	Homo sapiens	241-247
3129035-6	1988	The Km value of phenylalanine for the cytoplasmic form of phenylalanine hydroxylase is 0.32.10(-3) M, that for the membrane form is 1.66.10(-3) M. Both enzyme forms can bind to phenyl-Sepharose after their activation by the substrate, and they dissociate from the carrier after phenylalanine removal from the incubation mixture, which points to the intactness of the phenylalanine binding allosteric center in the membrane form of the enzyme.	acetophenone	16-22	phenylalanine hydroxylase	Rattus norvegicus	58-83
33885554-4	2021	The results of computations for several potential reaction pathways are juxtaposed with experiment-based calculations, which leads to stepwise mechanisms and energy profiles for the reactions of pinacolborane with benzaldehyde and acetophenone (in the presence of KF).	acetophenone	231-243	arylformamidase	Homo sapiens	264-266
3103131-2	1987	For example, in a reconstituted system containing rabbit liver microsomal P-450 form 2, NADPH-cytochrome P-450 reductase, and NADPH, cumyl hydroperoxide yields acetophenone and methane, but no cumyl alcohol is formed.	acetophenone	160-172	NADPH--cytochrome P450 reductase	Oryctolagus cuniculus	88-120
6143758-14	1984	Gel filtration of prereacted mixtures of [U-14C]phenylhydrazine plus hemoproteins resulted in co-chromatography of radioactivity, protein, and guanylate cyclase stimulating activity, and yielded a phenyl-hemoprotein binding stoichiometry of four under specified conditions (one phenyl/heme).	acetophenone	48-54	guanylate cyclase	Bos taurus	143-160
6699544-1	1984	Previous work has shown that the injection of antiidiotope antibodies specific for idiotopes of the germline-encoded anti-(4-hydroxy-3-nitro-phenyl) acetyl (NP) antibody B1-8 enhanced or suppressed the expression of B1-8 idiotopes in subsequent humoral anti-NP responses, depending on the dose and perhaps also the isotype of the injected antibody.	acetophenone	141-147	bradykinin receptor, beta 2	Mus musculus	170-174
6699544-1	1984	Previous work has shown that the injection of antiidiotope antibodies specific for idiotopes of the germline-encoded anti-(4-hydroxy-3-nitro-phenyl) acetyl (NP) antibody B1-8 enhanced or suppressed the expression of B1-8 idiotopes in subsequent humoral anti-NP responses, depending on the dose and perhaps also the isotype of the injected antibody.	acetophenone	141-147	bradykinin receptor, beta 2	Mus musculus	216-220
6299382-3	1983	Spin traps were also found to inhibit haemolysis and lipid peroxidation in phenylhydrazine-treated fresh human erythrocytes, with a concomitant production of phenyl radical spin adducts.	acetophenone	158-172	spindlin 1	Homo sapiens	0-4
6299382-3	1983	Spin traps were also found to inhibit haemolysis and lipid peroxidation in phenylhydrazine-treated fresh human erythrocytes, with a concomitant production of phenyl radical spin adducts.	acetophenone	158-172	spindlin 1	Homo sapiens	173-177
4030762-9	1985	Analyses of products formed from the interaction of cumene hydroperoxide with cytochrome P-450 showed that this substrate undergoes rearrangement also; 2-phenyl-1,2-propanediol was produced, together with cumyl alcohol and acetophenone.	acetophenone	223-235	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	78-94
6498204-7	1984	These findings suggest a model in which trehalase has two binding sites at the substrate-binding site, a phlorizin (glucosyl) and a phloretin (phenyl) binding site, analogous to the model proposed previously for the glucose carrier.	acetophenone	143-150	trehalase	Homo sapiens	40-49
33316359-0	2021	New lignans and acetophenone derivatives with alpha-glucosidase inhibitory activity from the leaves of Melicope patulinervia.	acetophenone	16-28	sucrase-isomaltase	Homo sapiens	46-63
33260981-1	2020	Kinetic studies and molecular modeling of human acetylcholinesterase (AChE) inhibition by a fluorinated acetophenone derivative, 1-(3-tert-butylphenyl)-2,2,2-trifluoroethanone (TFK), were performed.	acetophenone	104-116	acetylcholinesterase (Cartwright blood group)	Homo sapiens	48-68
32920141-2	2020	Here, a collection of acetylphenol analogues derived from paeonol and acetophenone were synthesized and evaluated for their alpha-glucosidase inhibitory activity.	acetophenone	70-82	sucrase-isomaltase	Homo sapiens	124-141
33260981-1	2020	Kinetic studies and molecular modeling of human acetylcholinesterase (AChE) inhibition by a fluorinated acetophenone derivative, 1-(3-tert-butylphenyl)-2,2,2-trifluoroethanone (TFK), were performed.	acetophenone	104-116	acetylcholinesterase (Cartwright blood group)	Homo sapiens	70-74
32343561-5	2020	The porphyrin (AlPor, AlPorF3 or AlPorF5) redox potentials are tuned by substitution of phenyl (Ph), 3,4,5-trifluorophenyl (PhF3) or 2,3,4,5,6-pentafluorophenyl (PhF5) groups in its meso positions.	acetophenone	88-94	PHD finger protein 3	Homo sapiens	124-128
32911196-5	2020	Utilizing information from molecular modelling of the hybrids to the anti-apoptotic Bcl-2 protein, we added substructures including phenyl, piperazine, piperidine, and morpholine rings to their frameworks.	acetophenone	132-138	BCL2 apoptosis regulator	Homo sapiens	84-89
32046403-3	2020	Apocynin, acetophenone with anti-oxidative and anti-inflammation activities, has been shown to protect against insulin resistance.	acetophenone	10-22	insulin	Homo sapiens	111-118
32015097-3	2020	We found Olfr923 to be one of the most sensitive ORs that is enriched by acetophenone.	acetophenone	73-85	olfactory receptor family 8 subfamily B member 56	Mus musculus	9-16
32015097-4	2020	Using a mouse line that genetically labels Olfr923-positive axons, we provided evidence that acetophenone activates the Olfr923 glomeruli in the olfactory bulb.	acetophenone	93-105	olfactory receptor family 8 subfamily B member 56	Mus musculus	43-50
32015097-4	2020	Using a mouse line that genetically labels Olfr923-positive axons, we provided evidence that acetophenone activates the Olfr923 glomeruli in the olfactory bulb.	acetophenone	93-105	olfactory receptor family 8 subfamily B member 56	Mus musculus	120-127
32015097-5	2020	Through molecular dynamics stimulations, we identified amino acid residues in the Olfr923 binding cavity that facilitate acetophenone binding.	acetophenone	121-133	olfactory receptor family 8 subfamily B member 56	Mus musculus	82-89
31384834-1	2019	Background: In continuation of our work, new diazenyl chalcones scaffolds (C-18 to C-27) were efficiently synthesized from substituted acetophenone azo dyes (A-E) by base catalyzed Claisen-Schmidt condensation with different substituted aromatic/heteroaromatic aldehydes.	acetophenone	135-147	Bardet-Biedl syndrome 9	Homo sapiens	75-79
31072245-0	2019	Benzonate derivatives of acetophenone as potent alpha-glucosidase inhibitors: synthesis, structure-activity relationship and mechanism.	acetophenone	25-37	sucrase isomaltase (alpha-glucosidase)	Mus musculus	48-65
31575771-6	2019	Murine in vivo and differentiated C2C12 myotube cell studies showed that 2-AA promotes ROS generation in skeletal muscle via the modulation of xanthine oxidase (XO) activity, NAD(P)H oxidase2 (NOX2) protein level, and the activity of antioxidant enzymes.	acetophenone	73-77	xanthine dehydrogenase	Mus musculus	143-159
31575771-6	2019	Murine in vivo and differentiated C2C12 myotube cell studies showed that 2-AA promotes ROS generation in skeletal muscle via the modulation of xanthine oxidase (XO) activity, NAD(P)H oxidase2 (NOX2) protein level, and the activity of antioxidant enzymes.	acetophenone	73-77	cytochrome b-245, beta polypeptide	Mus musculus	175-191
31575771-6	2019	Murine in vivo and differentiated C2C12 myotube cell studies showed that 2-AA promotes ROS generation in skeletal muscle via the modulation of xanthine oxidase (XO) activity, NAD(P)H oxidase2 (NOX2) protein level, and the activity of antioxidant enzymes.	acetophenone	73-77	cytochrome b-245, beta polypeptide	Mus musculus	193-197
30445058-5	2019	ATP and cyclic AMP production by control and OR10G7 small interfering RNA-transfected keratinocytes in response to odorant stimulation with acetophenone and eugenol was assessed.	acetophenone	140-152	olfactory receptor family 10 subfamily G member 7	Homo sapiens	45-51
30926317-6	2019	Rabbit DHRS11 also reduced alpha-dicarbonyl compounds, aldehydes and aromatic ketones (acetylbenzenes and acetylpyridines), and exhibited 3(17)beta-hydroxysteroid dehydrogenase activity.	acetophenone	87-101	LOW QUALITY PROTEIN: dehydrogenase/reductase SDR family member 11	Oryctolagus cuniculus	7-13
30292395-6	2019	RESULTS: Extinguishing fear toward Ace or Lyral of F0 male mice (F0-Extinguished) that had been fear conditioned with Ace or Lyral, respectively, results in F1-Extinguished offspring that do not demonstrate behavioral sensitivity to Ace or Lyral, respectively, and do not have enhanced representation for M71 or MOR23 odorant receptors in the olfactory system, as is observed in F1-Trained-Ace or F1-Trained-Lyral cohorts, respectively.	acetophenone	35-38	olfactory receptor family 8 subfamily A member 1	Mus musculus	305-308
30292395-6	2019	RESULTS: Extinguishing fear toward Ace or Lyral of F0 male mice (F0-Extinguished) that had been fear conditioned with Ace or Lyral, respectively, results in F1-Extinguished offspring that do not demonstrate behavioral sensitivity to Ace or Lyral, respectively, and do not have enhanced representation for M71 or MOR23 odorant receptors in the olfactory system, as is observed in F1-Trained-Ace or F1-Trained-Lyral cohorts, respectively.	acetophenone	35-38	olfactory receptor family 10 subfamily J member 5	Mus musculus	312-317
32254242-2	2018	Herein, we synthesized a novel phenyl-substituted imidazole-fused rhodamine analogue RV-1 with a long absorption wavelength at 573 nm and a large Stokes shift of about 82 nm for monitoring the changes in cellular viscosity.	acetophenone	31-37	Friend virus susceptibility 1	Mus musculus	85-89
28860658-0	2017	Modification of the response of olfactory receptors to acetophenone by CYP1a2.	acetophenone	55-67	cytochrome P450 family 1 subfamily A member 2	Homo sapiens	71-77
29850046-2	2018	Whereas the structure of the methyl-substituted derivative (HATNMe6) contains no solvent mol-ecules (C30H24N6), the hexa-phenyl-substituted structure (HATNPh6) contains two mol-ecules of di-chloro-methane (C60H36N6 2CH2Cl2).	acetophenone	121-127	hexosaminidase subunit alpha	Homo sapiens	116-120
29250404-1	2017	The condensation reaction of aceto-phenone (1-phenyl-ethan-1-one) with 2-nitro-benzaldehyde in the molten state yielded the expected chalcone, (E)-3-(2-nitro-phen-yl)-1-phenyl-prop-2-en-1-one, and, unexpectedly, the title compound, C30H22N2O6, which results from the syn head-to-head [2 + 2] cyclo-addition of the chalcone.	acetophenone	29-42	synemin	Homo sapiens	267-270
29250404-1	2017	The condensation reaction of aceto-phenone (1-phenyl-ethan-1-one) with 2-nitro-benzaldehyde in the molten state yielded the expected chalcone, (E)-3-(2-nitro-phen-yl)-1-phenyl-prop-2-en-1-one, and, unexpectedly, the title compound, C30H22N2O6, which results from the syn head-to-head [2 + 2] cyclo-addition of the chalcone.	acetophenone	44-64	synemin	Homo sapiens	267-270
28860658-5	2017	Among the CYPs tested, co-expression of CYP1a2 significantly affected the responses of various ORs, including MOR161-2, to acetophenone.	acetophenone	123-135	cytochrome P450 family 1 subfamily A member 2	Homo sapiens	40-46
28860658-5	2017	Among the CYPs tested, co-expression of CYP1a2 significantly affected the responses of various ORs, including MOR161-2, to acetophenone.	acetophenone	123-135	olfactory receptor family 8 subfamily B member 12	Mus musculus	110-118
28860658-6	2017	Conversion of acetophenone to methyl salicylate was observed in the medium of CYP1a2-expressing cells.	acetophenone	14-26	cytochrome P450 family 1 subfamily A member 2	Homo sapiens	78-84
28860658-7	2017	MOR161-2-expressing cells exhibited significantly greater responses to methyl salicylate than to acetophenone.	acetophenone	97-109	olfactory receptor family 8 subfamily B member 12	Mus musculus	0-8
28860658-9	2017	MOR161-2 responded to both acetophenone and methyl salicylate in vivo.	acetophenone	27-39	olfactory receptor family 8 subfamily B member 12	Mus musculus	0-8
28860658-10	2017	When the olfactory mucus was washed out by the injection of PBS to mouse nasal cavity, the response of MOR161-2 to acetophenone was reduced, while that to methyl salicylate did not change.	acetophenone	115-127	olfactory receptor family 8 subfamily B member 12	Mus musculus	103-111
28860658-11	2017	Our data suggest that CYP1a2 affects OR activation by converting acetophenone to methyl salicylate.	acetophenone	65-77	cytochrome P450 family 1 subfamily A member 2	Homo sapiens	22-28
28240894-4	2017	Here, some prenylated acetophenone dimers from Acronychia pedunculata have been identified for their dual inhibitory potency toward 5-LO and mPGES-1.	acetophenone	22-34	prostaglandin E synthase	Mus musculus	141-148
28685570-2	2017	This cross-coupling reaction includes the oxidative cleavage of sp2 C-N bonds of phenyl hydrazides to form a phenyl radical and the subsequent N-addition to cyanos to form new sp2 C-N bonds and provides efficient access to various N-phenyl amides in moderate to good yields under mild reaction conditions.	acetophenone	109-123	Sp2 transcription factor	Homo sapiens	64-67
28685570-2	2017	This cross-coupling reaction includes the oxidative cleavage of sp2 C-N bonds of phenyl hydrazides to form a phenyl radical and the subsequent N-addition to cyanos to form new sp2 C-N bonds and provides efficient access to various N-phenyl amides in moderate to good yields under mild reaction conditions.	acetophenone	109-123	Sp2 transcription factor	Homo sapiens	176-179
27545873-8	2017	We confirmed acetophenone as a specific TRPA1 agonist that activates the receptor in concentrations >3mM, whereas isophorone specifically activates TRPV1 in concentrations >100muM.	acetophenone	13-25	transient receptor potential cation channel, subfamily A, member 1	Mus musculus	40-45
27865994-3	2017	METHODS: We report the synthesis of new phenanthroline, phenyl and quinoline acyclic bisoxazole compounds in order to explore and evaluate the targeting to c-myc and human telomeric repeat 22AG G4 using FRET-melting, CD-melting, NMR, fluorescence titrations and FID assays.	acetophenone	56-62	MYC proto-oncogene, bHLH transcription factor	Homo sapiens	156-161
30108835-3	2017	Phenyl or pyrazolyl groups were the best in terms of affinity for the sigma1R and the 4-(1-methylpyrazol-5-yl) derivative, 12f, was the most selective.	acetophenone	0-6	sigma non-opioid intracellular receptor 1	Mus musculus	70-77
27637382-3	2016	Various fluorinated acetophenone derivatives bind to acetylcholinesterase with high affinity, including 2,2,2-trifluoro-1-(3-dimethylaminophenyl)ethanone (1) and 1-(3-tert-butylphenyl)-2,2,2-trifluoroethanone (2).	acetophenone	20-32	acetylcholinesterase (Cartwright blood group)	Homo sapiens	53-73
27014933-1	2016	This communication describes the two-electron oxidation of ((DIPP)CCC)NiX ((DIPP)CCC = bis(diisopropylphenyl-benzimidazol-2-ylidene)phenyl); X = Cl or Br) with halogen and halogen surrogates to form ((DIPP)CCC)NiX3.	acetophenone	102-108	BCL2 interacting protein 3 like	Homo sapiens	70-73
27396505-3	2016	Among these, phenyl, 4- and 2-chlorophenyl, 2-methoxyphenyl, 2-pyridyl, and 2-pyrimidyl derivatives 15, 24, 25, and 27-29 displayed nanomolar affinity values for the 5-HT7 receptor (Ki 23.5-52.0nM) and no affinity for the 5-HT1A receptor.	acetophenone	13-19	5-hydroxytryptamine receptor 1A	Homo sapiens	222-237
27011163-0	2016	Preparation of Pd-Loaded Hierarchical FAU Membranes and Testing in Acetophenone Hydrogenation.	acetophenone	67-79	FAU ubiquitin like and ribosomal protein S30 fusion	Homo sapiens	38-41
27011163-1	2016	Pd-loaded hierarchical FAU (Pd-FAU) membranes, containing an intrinsic secondary non-zeolitic (meso)porosity, were prepared and tested in the catalytic transfer hydrogenation of acetophenone (AP) to produce phenylethanol (PE), an industrially relevant product.	acetophenone	178-190	FAU ubiquitin like and ribosomal protein S30 fusion	Homo sapiens	23-26
27011163-1	2016	Pd-loaded hierarchical FAU (Pd-FAU) membranes, containing an intrinsic secondary non-zeolitic (meso)porosity, were prepared and tested in the catalytic transfer hydrogenation of acetophenone (AP) to produce phenylethanol (PE), an industrially relevant product.	acetophenone	178-190	FAU ubiquitin like and ribosomal protein S30 fusion	Homo sapiens	31-34
26618894-6	2016	Complex [Re(p-NTol)Cl(L(2))(PPh3)2]PF6 (13) is the catalyst of choice for oxidation of 1-phenylethanol to acetophenone (in 80% yield; turnover number attained 290 after 30 h) and cyclooctanol to cyclooctanone (in 88% yield).	acetophenone	106-118	protein phosphatase 4 catalytic subunit	Homo sapiens	28-32
26618894-6	2016	Complex [Re(p-NTol)Cl(L(2))(PPh3)2]PF6 (13) is the catalyst of choice for oxidation of 1-phenylethanol to acetophenone (in 80% yield; turnover number attained 290 after 30 h) and cyclooctanol to cyclooctanone (in 88% yield).	acetophenone	106-118	sperm associated antigen 17	Homo sapiens	35-38
25406399-3	2015	The latter isomerized via the addition of the phenyl radical to the terminal C1/C4 carbon atoms through submerged barriers forming resonantly stabilized free radicals C11H13, which then underwent cis-trans isomerization followed by ring closure.	acetophenone	46-60	heterogeneous nuclear ribonucleoprotein C	Homo sapiens	77-82
26473832-6	2015	Flavonoid glucosides and acetophenone derivatives showed aldose reductase and alpha-glucosidase inhibition, and could explain the traditional use of Myrcia species to treat diabetes.	acetophenone	25-37	aldo-keto reductase family 1 member B	Homo sapiens	57-73
26473832-6	2015	Flavonoid glucosides and acetophenone derivatives showed aldose reductase and alpha-glucosidase inhibition, and could explain the traditional use of Myrcia species to treat diabetes.	acetophenone	25-37	sucrase-isomaltase	Homo sapiens	78-95
25611197-2	2015	The new well-defined [Ni(IPr*)(cin)Cl] (1 c) pre-catalyst showed great efficiency for this transformation, allowing the coupling of a wide range of ketones, including acetophenone derivatives, with various functionalised aryl chlorides.	acetophenone	167-179	pyridoxal phosphatase	Homo sapiens	31-34
25877513-6	2015	Superior adsorption was dominated by various interaction modes including pi-pi electron donor-acceptor interactions between the pi-electron-deficient phenyls of the NACs and the pi-electron-rich matrix of the graphene nanosheets, and the charge electrostatic and polar interactions between the defect sites of graphene nanosheets and the -NO2 of the NAC.	acetophenone	150-157	synuclein alpha	Homo sapiens	165-168
24884962-2	2014	The reaction of phenyl with 1,2-butadiene is initiated by adding the phenyl radical with its radical center to the pi electron density at the C1/C3 carbon atom of 1,2-butadiene.	acetophenone	16-22	heterogeneous nuclear ribonucleoprotein C	Homo sapiens	142-147
24928349-8	2014	Activation of P2X1 receptors had more profound inhibitory effects on benzaldehyde-evoked intracellular calcium elevation than on acetophenone-evoked responses within the same neurons, and the reverse was true when P2Y2 receptors were activated.	acetophenone	129-141	purinergic receptor P2X 1	Homo sapiens	14-18
25014710-1	2014	The first asymmetric gamma-alkoxyallylboration of representative ketones provides beta-alkoxy tert-homoallylic alcohols 10 whose diastereoselectivities range from 99% syn (acetophenone) to 99% anti (pinacolone) both with high ee (>95%).	acetophenone	172-184	synemin	Homo sapiens	167-170
24577918-6	2014	In addition, HPRT assay showed the mutagenic effect of photosensitizer, acetophenone.	acetophenone	72-84	hypoxanthine-guanine phosphoribosyltransferase	Cricetulus griseus	13-17
24695705-5	2014	Here we exposed MOR23-green fluorescent protein (GFP) and M71-GFP mice to lyral or acetophenone, ligands for MOR23 or M71, respectively.	acetophenone	83-95	olfactory receptor family 10 subfamily J member 5	Mus musculus	109-114
24695705-5	2014	Here we exposed MOR23-green fluorescent protein (GFP) and M71-GFP mice to lyral or acetophenone, ligands for MOR23 or M71, respectively.	acetophenone	83-95	olfactory receptor 7 complex	Mus musculus	118-121
24078149-4	2014	The second couples the CV2025 omega-TAm with alcohol dehydrogenase and glucose dehydrogenase for removal of the acetophenone (AP) by-product by in situ conversion to (R)-1-phenylethanol.	acetophenone	112-124	hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase	Homo sapiens	71-92
22833116-1	2012	Cage dodecaphenylsilsesquioxane (T12-Phenyl) was synthesized in a one batch, mildly basic aqueous solution under room temperature conditions using a trialkoxysilane precursor.	acetophenone	37-43	CD6 molecule	Homo sapiens	33-36
23802426-0	2013	Design, synthesis, and biological evaluation of acetophenone derivatives as dual binding acetylcholinesterase inhibitors.	acetophenone	48-60	acetylcholinesterase (Cartwright blood group)	Homo sapiens	89-109
23802426-1	2013	As part of a project aimed at developing new agents for potential application in Alzheimer"s disease, a new series of acetophenone derivatives which possess alkylamine side chains were designed, synthesized and assayed as acetylcholinesterase (AChE) inhibitors that could simultaneously bind to the peripheral and catalytic sites of the enzyme.	acetophenone	118-130	acetylcholinesterase (Cartwright blood group)	Homo sapiens	222-242
23802426-1	2013	As part of a project aimed at developing new agents for potential application in Alzheimer"s disease, a new series of acetophenone derivatives which possess alkylamine side chains were designed, synthesized and assayed as acetylcholinesterase (AChE) inhibitors that could simultaneously bind to the peripheral and catalytic sites of the enzyme.	acetophenone	118-130	acetylcholinesterase (Cartwright blood group)	Homo sapiens	244-248
23426982-4	2013	We find that the debromination reaction results from the electronic transitions from pi to sigma* orbitals when nona-BDEs are exposed to UV-light in the sunlight region, at which point the two low-lying excited states for each nona-BDE are pisigma*(5Br) and pisigma*(4Br), which correlate to the sigma* orbitals located on the penta-Br and tetra-Br substituted phenyls, respectively.	acetophenone	361-368	homeobox D13	Homo sapiens	117-120
23585037-4	2013	Furthermore, this expression and functional system has been used to show that the preincubation of Human Odorant Binding Protein 2A decrease the calcium response of OR 17-210 following stimulation by acetophenone and beta ionone.	acetophenone	200-212	odorant binding protein 2A	Homo sapiens	105-131
24292232-3	2014	When an odor (acetophenone) that activates a known odorant receptor (Olfr151) was used to condition F0 mice, the behavioral sensitivity of the F1 and F2 generations to acetophenone was complemented by an enhanced neuroanatomical representation of the Olfr151 pathway.	acetophenone	14-26	olfactory receptor family 6 subfamily F member 2	Mus musculus	51-67
24292232-3	2014	When an odor (acetophenone) that activates a known odorant receptor (Olfr151) was used to condition F0 mice, the behavioral sensitivity of the F1 and F2 generations to acetophenone was complemented by an enhanced neuroanatomical representation of the Olfr151 pathway.	acetophenone	14-26	olfactory receptor family 8 subfamily A member 1	Mus musculus	69-76
24292232-3	2014	When an odor (acetophenone) that activates a known odorant receptor (Olfr151) was used to condition F0 mice, the behavioral sensitivity of the F1 and F2 generations to acetophenone was complemented by an enhanced neuroanatomical representation of the Olfr151 pathway.	acetophenone	14-26	olfactory receptor family 8 subfamily A member 1	Mus musculus	251-258
24292232-3	2014	When an odor (acetophenone) that activates a known odorant receptor (Olfr151) was used to condition F0 mice, the behavioral sensitivity of the F1 and F2 generations to acetophenone was complemented by an enhanced neuroanatomical representation of the Olfr151 pathway.	acetophenone	168-180	olfactory receptor family 6 subfamily F member 2	Mus musculus	51-67
24292232-3	2014	When an odor (acetophenone) that activates a known odorant receptor (Olfr151) was used to condition F0 mice, the behavioral sensitivity of the F1 and F2 generations to acetophenone was complemented by an enhanced neuroanatomical representation of the Olfr151 pathway.	acetophenone	168-180	olfactory receptor family 8 subfamily A member 1	Mus musculus	69-76
23458186-0	2013	Bis(oxazolinyl)phenyl-ligated rare-earth-metal complexes: highly regioselective catalysts for cis-1,4-polymerization of isoprene.	acetophenone	15-21	cytokine inducible SH2 containing protein	Homo sapiens	94-99
22532294-7	2012	Concerted coordination of acetophenone and dual hydrogen-atom transfer from the PNP arm and the coordinated ethanol to, respectively, the carbonyl carbon and oxygen atoms, leads to the dearomatized complex [(iPr-PNP*)Fe(CO)(EtO)(MeCH(OH)Ph)] (32).	acetophenone	26-38	RUNX1 partner transcriptional co-repressor 1	Homo sapiens	224-227
22497458-3	2012	The reaction is initiated by a barrierless addition of the phenyl radical to the terminal carbon atom of the 1,3-butadiene (C1/C4) to form a bound intermediate; the latter underwent hydrogen elimination from the terminal CH(2) group of the 1,3-butadiene molecule leading to 1-phenyl-trans-1,3-butadiene through a submerged barrier.	acetophenone	59-73	heterogeneous nuclear ribonucleoprotein C	Homo sapiens	124-129
21615508-1	2011	Two natural acetophenone derivatives, 2,5-dihydroxyacetophenone (2,5-DHAP) and 2,6-DHAP, were purified from Cynanchum bungei and identified as murine tyrosinase inhibitors.	acetophenone	12-24	tyrosinase	Mus musculus	150-160
22429107-6	2012	The modeling results indicated that the concentration of acetylene and propargyl radicals, the main PAH precursors, as well as the PAH amounts were lower in the flame of the ethanol-benzene fuel mixture than in the pure benzene flame and that all of the formed PAHs were issued from the phenyl radical.	acetophenone	287-301	phenylalanine hydroxylase	Homo sapiens	131-134
21671642-7	2011	Since it has been proposed that the phenyl radical metabolite leads to protein radical formation on MPO, we investigated the effect of LA and DHA in immuno-spin trapping experiments with MPO-containing HL-60 cell lysate.	acetophenone	36-50	myeloperoxidase	Homo sapiens	100-103
21675799-2	2011	The turnover frequency of the hydrogenation of acetophenone reaches about 35,000 min(-1) in the best case, affording 1-phenylethanol in >99% ee.	acetophenone	47-59	CD59 molecule (CD59 blood group)	Homo sapiens	81-87
19233899-3	2009	The 3"-C-branched p-methylphenyl (compound 1) and 3-CF(3)-4-Cl-phenyl (compound 7) thiourea derivatives of beta-dThd showed competitive inhibition of TK-2 when dThd was used as the variable substrate (K(i) values, 0.40 and 0.05 microM, respectively), but uncompetitive inhibition in the presence of variable concentrations of ATP (K(i) values, 15 and 2.0 microM, respectively).	acetophenone	26-32	thymidine kinase 2	Homo sapiens	150-154
20026676-6	2010	Here, we identify six different SNPs that are associated with variation in responses to a structurally similar odorant, acetophenone, in the same Obp genes.	acetophenone	120-132	Optix-binding protein	Drosophila melanogaster	146-149
20026676-8	2010	We found that the 610G allele is associated with higher response scores to acetophenone than the 610A allele, but with lower expression of Obp99a, suggesting that binding of acetophenone to Opb99a might limit rather than facilitate access to odorant receptors.	acetophenone	174-186	Odorant-binding protein 99a	Drosophila melanogaster	139-145
21582758-2	2009	The benzene ring of the hexa-hydro-pyrroloisoquinoline ring system makes dihedral angles of 83.43 (6) and 61.99 (10) , respectively, with the phenyl and pyrrole rings.	acetophenone	142-148	hexosaminidase subunit alpha	Homo sapiens	24-28
21837179-1	2011	In the title compound, C(24)H(25)NO, the phenyl and diphenyl-methanol substituents are syn to each other.	acetophenone	41-47	synemin	Homo sapiens	87-90
20199096-2	2010	We have previously shown that the metabolism of two aromatic amine drugs by human myeloperoxidase (MPO) results in phenyl radical metabolite formation and also in protein free radical formation on MPO.	acetophenone	115-129	myeloperoxidase	Homo sapiens	82-97
20199096-2	2010	We have previously shown that the metabolism of two aromatic amine drugs by human myeloperoxidase (MPO) results in phenyl radical metabolite formation and also in protein free radical formation on MPO.	acetophenone	115-129	myeloperoxidase	Homo sapiens	99-102
20199096-10	2010	Interestingly, we found that only those aniline derivatives that produced a phenyl radical also formed MPO*.	acetophenone	76-90	myeloperoxidase	Homo sapiens	103-106
20199096-11	2010	We propose that the phenyl radical is the reactive free radical metabolite responsible for generating the MPO*.	acetophenone	20-34	myeloperoxidase	Homo sapiens	106-110
19928821-1	2010	Singlet-singlet energy transfer in self-assembled via axial coordination of imidazole-appended (at different positions of one of the meso-phenyl entities) free-base tetraphenylporphyrin, H(2)PIm, to either zinc phthalocyanine, ZnPc, or zinc naphthalocyanine, ZnNc, dyads is investigated in noncoordinating solvents, o-dichlorobenzene and toluene, using both steady-state and time-resolved transient absorption techniques.	acetophenone	138-144	Pim-1 proto-oncogene, serine/threonine kinase	Homo sapiens	191-194
20024111-5	2009	Barriers to rotation around the syn phenyl-imino bond are also reported (10.5-11.1 kcal mol(-1)).	acetophenone	36-42	synemin	Homo sapiens	32-35
19407445-2	2009	METHODS: An initial structure-activity relationship study of the NF-kappaB inhibitory activity of acetophenone-type compounds using electrophoretic mobility shift assay and Western blot analysis is presented.	acetophenone	98-110	nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105	Mus musculus	65-74
19052201-4	2008	Transgenic mice labeled at the M71 odorant receptor (specifically activated by the odorant acetophenone) were behaviorally trained with olfactory-dependent fear conditioning or conditioned place preference using acetophenone.	acetophenone	91-103	olfactory receptor family 8 subfamily A member 1	Mus musculus	31-51
19109912-5	2008	The M71 transgenic mice readily detect other odors in the presence of acetophenone.	acetophenone	70-82	olfactory receptor 7 complex	Mus musculus	4-7
18318476-6	2008	The DFT-PBE results suggest that this reaction is driven to the (R)-product only by the process of binding the acetophenone to the active site of the trans-Ru(H) 2(S, S-dpen)(S-tolbinap) catalyst.	acetophenone	111-123	enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase	Homo sapiens	8-11
18489081-9	2008	The DMPO adducts of MPO metabolism, as analyzed by electron spin resonance spectroscopy, included a nitrogen-centered radical and a phenyl radical derived from PA, either of which may be involved in the free radical formation on MPO.	acetophenone	132-146	myeloperoxidase	Homo sapiens	5-8
18489081-9	2008	The DMPO adducts of MPO metabolism, as analyzed by electron spin resonance spectroscopy, included a nitrogen-centered radical and a phenyl radical derived from PA, either of which may be involved in the free radical formation on MPO.	acetophenone	132-146	myeloperoxidase	Homo sapiens	20-23
17602675-8	2007	When analyzed by electron spin resonance spectroscopy, we detected a phenyl radical adduct, derived from AG, which may be involved in the free radical formation on MPO.	acetophenone	69-83	myeloperoxidase	Homo sapiens	164-167
18006320-1	2008	Stereoselective reductive metabolism of various p-substituted acetophenone derivatives was studied using isolated rat liver 3alpha-hydroxysteroid dehydrogenase (3alpha-HSD).	acetophenone	62-74	aldo-keto reductase family 1, member C14	Rattus norvegicus	124-159
18006320-1	2008	Stereoselective reductive metabolism of various p-substituted acetophenone derivatives was studied using isolated rat liver 3alpha-hydroxysteroid dehydrogenase (3alpha-HSD).	acetophenone	62-74	aldo-keto reductase family 1, member C14	Rattus norvegicus	161-171
18006776-1	2007	PURPOSE: 1,1-Bis(3"-indolyl)-1-(p-substitutedphenyl)methanes [methylene-substituted diindolylmethanes (C-DIM)] containing p-trifluoromethyl, p-t-butyl, and p-phenyl substituents activate peroxisome proliferator-activated receptor gamma (PPARgamma) and inhibit growth of several different cancer cell lines through receptor-dependent and receptor-independent pathways.	acetophenone	45-51	peroxisome proliferator activated receptor gamma	Homo sapiens	187-235
18006776-1	2007	PURPOSE: 1,1-Bis(3"-indolyl)-1-(p-substitutedphenyl)methanes [methylene-substituted diindolylmethanes (C-DIM)] containing p-trifluoromethyl, p-t-butyl, and p-phenyl substituents activate peroxisome proliferator-activated receptor gamma (PPARgamma) and inhibit growth of several different cancer cell lines through receptor-dependent and receptor-independent pathways.	acetophenone	45-51	peroxisome proliferator activated receptor gamma	Homo sapiens	237-246
18242988-2	2008	Systematic modification of the benzimidazole core and tethered acetophenone moiety established tractable SAR of analogs with improved physicochemical properties and sub-micromolar activity across both human and murine receptors.	acetophenone	63-75	sarcosine dehydrogenase	Homo sapiens	105-108
19202742-1	2008	Some acetophenone (CAS 98-86-2) derived bis Mannich bases, bis-(3-aryl-3-oxo-propyl)-methylamine hydrochlorides (B1-B5) and representative piperidinols, 4-aryl-3-arylcarbonyl-1-methyl-4-piperidinol hydrochlorides (C1, C2 and C5), which are the structural isomers of B1, B2 and B5, were synthesized and their effects on DNA topoisomerase I were tested.	acetophenone	5-17	immunoglobulin kappa variable 7-3 (pseudogene)	Homo sapiens	266-279
17226937-6	2007	In the proposed reaction mechanism, the active-site cysteine residue of GSTO1-1 reacts with the S-(phenacyl)glutathione substrate to give an acetophenone and a mixed disulfide with the active-site cysteine; a second thiol substrate (e.g., glutathione or 2-mercaptoethanol) reacts with the active-site disulfide to regenerate the catalytically active enzyme and to form a mixed disulfide.	acetophenone	141-153	glutathione S-transferase omega 1	Rattus norvegicus	72-79
17441044-0	2006	Mechanism of asymmetric hydrogenation of acetophenone catalyzed by chiral eta(6)-arene-N-tosylethylenediamine-ruthenium(II) complexes.	acetophenone	41-53	endothelin receptor type A	Homo sapiens	74-77
17441044-2	2006	[Ru(OSO2CF3){(S,S)-TsNCH(C6H5)CH(C6H5)NH2}(eta(6)-p-cymene)] catalyzes the asymmetric hydrogenation of acetophenone in methanol to afford (S)-1-phenylethanol with 96% ee in 100% yield.	acetophenone	103-115	endothelin receptor type A	Homo sapiens	43-46
16448083-1	2006	An acetophenone containing PNA-based reagent was designed for the direct and site-specific synthesis of a cis-syn thymidine dimer lesion in genomic DNA.	acetophenone	3-15	synemin	Homo sapiens	91-94
15604828-3	2004	Using this whole-cell biocatalyst, efficient conversion of prochiral ketones to chiral alcohols was achieved: 66% acetophenone was reduced to (R)-phenylethanol over 12 h, whereas only 19% (R)-phenylethanol was formed under the same conditions with cells containing ADH and FDH genes but without PNT genes.	acetophenone	114-126	alcohol dehydrogenase 5 (class III), chi polypeptide	Homo sapiens	273-276
16298757-10	2006	ESR spin-trapping experiments showed that the phenyl radical was formed during the reaction of 4-hydrazinobenzoic acid in the presence of Cu(II) and catalase.	acetophenone	46-60	catalase	Bos taurus	149-157
16397256-1	2006	1,1-Bis(3"-indolyl)-1-(p-substitutedphenyl)methanes containing p-trifluoromethyl (DIM-C-pPhCF3), p-t-butyl (DIM-C-pPhtBu), and phenyl (DIM-C-pPhC6H5) substituents have been identified as a new class of peroxisome proliferator-activated receptor gamma (PPARgamma) agonists that exhibit antitumorigenic activity.	acetophenone	36-42	peroxisome proliferator activated receptor gamma	Homo sapiens	202-250
16397256-1	2006	1,1-Bis(3"-indolyl)-1-(p-substitutedphenyl)methanes containing p-trifluoromethyl (DIM-C-pPhCF3), p-t-butyl (DIM-C-pPhtBu), and phenyl (DIM-C-pPhC6H5) substituents have been identified as a new class of peroxisome proliferator-activated receptor gamma (PPARgamma) agonists that exhibit antitumorigenic activity.	acetophenone	36-42	peroxisome proliferator activated receptor gamma	Homo sapiens	252-261
15792487-8	2005	The dihydrides containing amino groups and cis-PPh3 groups, i.e., c,c-2a or c,c-2b, are active precatalysts for the H2-hydrogenation of acetophenone (neat or in benzene) under mild reaction conditions, whereas those with trans-PPh3 groups, c,t-2a and c,t-2b are much less active.	acetophenone	136-148	protein phosphatase 4 catalytic subunit	Homo sapiens	47-51
15792487-8	2005	The dihydrides containing amino groups and cis-PPh3 groups, i.e., c,c-2a or c,c-2b, are active precatalysts for the H2-hydrogenation of acetophenone (neat or in benzene) under mild reaction conditions, whereas those with trans-PPh3 groups, c,t-2a and c,t-2b are much less active.	acetophenone	136-148	secretoglobin family 2B member 3, pseudogene	Homo sapiens	78-82
15792487-8	2005	The dihydrides containing amino groups and cis-PPh3 groups, i.e., c,c-2a or c,c-2b, are active precatalysts for the H2-hydrogenation of acetophenone (neat or in benzene) under mild reaction conditions, whereas those with trans-PPh3 groups, c,t-2a and c,t-2b are much less active.	acetophenone	136-148	protein phosphatase 4 catalytic subunit	Homo sapiens	227-231
12027671-10	2002	The transformation of p-quinone 2 into acetophenone 3 might contribute to the chemistry of tocopherols oxidized at C-4, i.e., 4-hydroxy-alpha-tocopherol and 4-oxo-alpha-tocopherol, which have been proposed as precursors of natural vitamin E metabolites.	acetophenone	39-51	complement C4A (Rodgers blood group)	Homo sapiens	115-118
12478754-1	2002	Exposure of tertiary thioamides to (E)-1-hexenyl(phenyl)-lambda 3-iodane results in vinylic SN2 reaction to give the inverted (Z)-S-vinylthioimidonium salts, which under alkaline hydrolysis (Na2CO3 or K2CO3) selectively afford amides, while (Z)-S-vinyl thioesters are obtained in high yields via the hydrolysis under acidic conditions (HCl).	acetophenone	49-56	solute carrier family 38 member 5	Homo sapiens	92-95
11806709-4	2002	Increasing the size of the RHS sulfonamide substituent with phenyl or p-toluene afforded compounds with good potency and functional selectivity (beta(3) AR pEC(50) greater than 8; beta(1) and beta(2) AR selectivity greater than 40- and 500-fold, respectively).	acetophenone	60-66	adrenergic receptor, beta 3	Mus musculus	145-155
11029216-2	2000	Photolysis of mercaptoundecanophenone-modified gold colloid, MUP-MPC, generates free acetophenone in solution and the nonene-modified MPC via the triplet excited state and the 1,4-biradical intermediate.	acetophenone	85-97	major urinary protein, pseudogene	Homo sapiens	61-64
12572525-1	2002	Some acetophenone derived bis Mannich bases (B1-B5) and piperidinols (C1, C4), which are the structural isomers of B1 and B4, and also quaternary piperidine derivative C6 were synthesized and studied for anticonvulsant activity.	acetophenone	5-17	immunoglobulin kappa variable 7-3 (pseudogene)	Homo sapiens	115-124
11812825-5	2001	It is concluded that acetophenone derivatives, which produce radicals upon photolysis, in particular the hydroxy (AP-OH) and tert-butoxy (AP-O(t)Bu) derivatives, are more effective in oxidizing DNA.	acetophenone	21-33	aminopeptidase O (putative)	Homo sapiens	114-118
8824622-3	1996	In anaerobic suspensions of strain EB1 cells metabolizing ethylbenzene, the transient formation and consumption of 1-phenylethanol, acetophenone, and an as yet unidentified compound were observed.	acetophenone	132-144	microtubule associated protein RP/EB family member 1	Homo sapiens	35-38
10537071-5	1999	The binding of zinc by the small myelin-associated glycoprotein induces a conformational change that enables the protein to reversibly bind to a hydrophobic phenyl-Sepharose matrix.	acetophenone	157-163	myelin associated glycoprotein	Homo sapiens	33-63
10222230-2	1999	Demethylation activities of either truncated 2B4 with N-methylaniline, N,N-dimethylaniline, and d-benzphetamine were lower than those of liver microsomal 2B4, whereas the rate of 1-phenylethanol oxidation to acetophenone catalyzed by liver microsomal and truncated 2B4 enzymes was nearly the same.	acetophenone	208-220	CD244 molecule	Homo sapiens	45-48
9655332-1	1998	We have determined the 2.5 A structure (Rcryst = 20.5%, Rfree = 28.5%) of a complex between human cathepsin S and the potent, irreversible inhibitor 4-morpholinecarbonyl-Phe-hPhe-vinyl sulfone-phenyl.	acetophenone	193-199	cathepsin S	Homo sapiens	98-109
10482506-12	1999	strain EB1 cells that were grown anaerobically on ethylbenzene, 1-phenylethanol, and acetophenone, but these activities were absent in benzoate-grown cells.	acetophenone	85-97	microtubule associated protein RP/EB family member 1	Homo sapiens	7-10
10941798-5	1999	These results suggest that strain EbN1 degrades ethylbenzene via 1-phenylethanol and acetophenone as intermediates, and that acetophenone is subsequently carboxylated.	acetophenone	85-97	potassium voltage-gated channel subfamily Q member 2	Homo sapiens	34-38
10941798-5	1999	These results suggest that strain EbN1 degrades ethylbenzene via 1-phenylethanol and acetophenone as intermediates, and that acetophenone is subsequently carboxylated.	acetophenone	125-137	potassium voltage-gated channel subfamily Q member 2	Homo sapiens	34-38
10941798-8	1999	In accordance with our findings from these studies, two-dimensional gel electrophoretic analysis of extracts of cells grown on benzoate, acetophenone, ethylbenzene, or toluene showed that a number of substrate-specific proteins were induced in strain EbN1.	acetophenone	137-149	potassium voltage-gated channel subfamily Q member 2	Homo sapiens	251-255