PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
32347981-8	2021	The saturated aldehydes Nonanal and Decanal (known skin metabolites) and the aromatic aldehyde Benzaldehyde (known skin and Staphylococcus epidermidis metabolite) were shown to induce the Nrf2-keap1 pathway in human keratinocytes.	benzaldehyde	95-107	NFE2 like bZIP transcription factor 2	Homo sapiens	188-192
32559510-1	2020	An efficient three component coupling of aromatic aldehyde, deoxy sugar based alkyne (alpha-2-deoxy propargyl glycoside) and heterocyclic amine have been refluxed to synthesize stereoselective chiral propargylamines with good to excellent yield using only CuI catalyst along with bifunctional ligand l-proline.	benzaldehyde	41-58	glycoprotein hormone subunit alpha 2	Homo sapiens	86-93
32559510-4	2020	The ligand l-proline was used for the first time in enantioselective A3-coupling reaction of alpha-2-deoxy propargyl glycosides involving substituted aromatic aldehyde and heterocyclic amines.	benzaldehyde	150-167	glycoprotein hormone subunit alpha 2	Homo sapiens	93-100
32496054-12	2020	Cinnamaldehyde and benzaldehyde were found to be the most potent inhibitors of microsomal CYP2A6 of the flavoring agents tested, with identified IC50 values of 1.1 muM and 3.0 muM, respectively.	benzaldehyde	19-31	cytochrome P450 family 2 subfamily A member 6	Homo sapiens	90-96
33063315-9	2020	Moreover, ethyl butyrate, benzaldehyde, and 2-heptanone, when added, had evident inhibitory or masking effects on the AI of "sour," "rancid," and "animalic (goat)" attributes.	benzaldehyde	26-38	membrane bound O-acyltransferase domain containing 4	Homo sapiens	157-161
32846602-5	2020	The Strecker aldehydes benzaldehyde and 2-methylbutanal resulted as effective markers to correlate with the initial lactase purity during storage.	benzaldehyde	23-35	lactase	Homo sapiens	116-123
33533423-3	2020	Compounds 4-X-benzylidene-4-carboxy aniline (X = H, F, Cl, Br, CH3, OCH3) 1b-6b were synthesized by the reaction of benzaldehyde and its substituted derivatives with 4-aminobenzoic acid using absolute ethanol as the solvent.	benzaldehyde	116-128	chromosome 12 open reading frame 73	Homo sapiens	59-61
32347981-8	2021	The saturated aldehydes Nonanal and Decanal (known skin metabolites) and the aromatic aldehyde Benzaldehyde (known skin and Staphylococcus epidermidis metabolite) were shown to induce the Nrf2-keap1 pathway in human keratinocytes.	benzaldehyde	95-107	kelch like ECH associated protein 1	Homo sapiens	193-198
31066398-3	2019	Treatment of 6a with non-conjugated small molecules such as phenyl isocyanates, phenyl isothiocyanate, and benzaldehyde resulted in formation of Sc/gamma-C [4 + 2] cycloaddition products 7-9 because of nucleophilic reactivity at the beta-diketiminato gamma-carbon, with retention of ScP interactions.	benzaldehyde	107-119	interleukin 2 receptor subunit gamma	Homo sapiens	148-155
31113817-6	2019	Gene-drug pairings linked by pathways or functions show specific correlations to isoforms compared with composite gene expression, including ALKBH2-benzaldehyde, AKT3-vandetanib, BCR-imatinib, CDK1 and 20-palbociclib, CASP1-imexon, and FGFR3-pazopanib.	benzaldehyde	148-160	alkB homolog 2, alpha-ketoglutarate dependent dioxygenase	Homo sapiens	141-147
31066398-3	2019	Treatment of 6a with non-conjugated small molecules such as phenyl isocyanates, phenyl isothiocyanate, and benzaldehyde resulted in formation of Sc/gamma-C [4 + 2] cycloaddition products 7-9 because of nucleophilic reactivity at the beta-diketiminato gamma-carbon, with retention of ScP interactions.	benzaldehyde	107-119	urocortin 3	Homo sapiens	283-286
30768969-13	2019	The most efficient of the tested substrates were comparable to benzaldehyde and p-anisaldehyde known as the best aromatic aldehyde substrates of plant cytosolic ALDH2s in vitro.	benzaldehyde	63-75	aldehyde dehydrogenase 2	Zea mays	161-166
30768969-13	2019	The most efficient of the tested substrates were comparable to benzaldehyde and p-anisaldehyde known as the best aromatic aldehyde substrates of plant cytosolic ALDH2s in vitro.	benzaldehyde	113-130	aldehyde dehydrogenase 2	Zea mays	161-166
30521138-4	2019	Presented in this report are the synthesis and biological evaluation of ALDH1A1-selective chemical probes composed of an aromatic aldehyde derived from N,N-diethylamino benzaldehyde (DEAB) linked to a fluorinated pyridine ring either via an amide or amine linkage.	benzaldehyde	121-138	aldehyde dehydrogenase 1 family member A1	Homo sapiens	72-79
30543227-5	2019	X-ray photoelectron spectroscopy reveals that the high ratio of Pd2+ to Pd0 in the surface of Pd-Pb NPs enhances the benzaldehyde productivity, and the electronic modification of the Pd3Pb NCs boosts the benzaldehyde selectivity.	benzaldehyde	117-129	PAF1 homolog, Paf1/RNA polymerase II complex component	Homo sapiens	64-67
30543227-5	2019	X-ray photoelectron spectroscopy reveals that the high ratio of Pd2+ to Pd0 in the surface of Pd-Pb NPs enhances the benzaldehyde productivity, and the electronic modification of the Pd3Pb NCs boosts the benzaldehyde selectivity.	benzaldehyde	204-216	PAF1 homolog, Paf1/RNA polymerase II complex component	Homo sapiens	64-67
30382490-3	2019	OBJECTIVES: The aim of this work was to study the effect of five important phenothiazine drugs on AOX activity using benzaldehyde and phenanthridine as aldehyde and N-heterocyclic substrates, respectively.	benzaldehyde	117-129	acyl-CoA oxidase 1	Rattus norvegicus	98-101
30382490-6	2019	RESULTS: All phenothiazines could inhibit AOX activity measured either by phenanthridine or benzaldehyde with almost no effect on XO activity.	benzaldehyde	92-104	acyl-CoA oxidase 1	Rattus norvegicus	42-45
30382490-7	2019	In the case of benzaldehyde oxidation, the lowest and highest half-maximal inhibitory concentration (IC50) values were obtained for promethazine (IC50 = 0.9 microM), and trifluoperazine (IC50 = 3.9 microM), respectively; whereas perphenazine (IC50 = 4.3 microM), and trifluoperazine (IC50 = 49.6 microM) showed the strongest and weakest inhibitory activity against AOX-catalyzed phenanthridine oxidation, respectively.	benzaldehyde	15-27	acyl-CoA oxidase 1	Rattus norvegicus	365-368
30439624-3	2019	The biosensing approach implied the use of ITO electrode coated with poly(phosphazene) polymer including benzaldehyde groups attached with CDH22 antibody and CDH22 antigens.	benzaldehyde	105-117	cadherin 22	Homo sapiens	139-144
30439624-4	2019	Benzaldehyde side groups containing poly(phosphazene) film coated disposable ITO electrode were utilized as an immunosensing platform and anti-CDH22 antibodies bound to aldehyde groups of benzaldehyde substituted poly(phosphazene) (P-PHP) covalently.	benzaldehyde	0-12	cadherin 22	Homo sapiens	143-148
30439624-0	2019	Electrochemical immunosensor for CDH22 biomarker based on benzaldehyde substituted poly(phosphazene) modified disposable ITO electrode: A new fabrication strategy for biosensors.	benzaldehyde	58-70	cadherin 22	Homo sapiens	33-38
30439624-4	2019	Benzaldehyde side groups containing poly(phosphazene) film coated disposable ITO electrode were utilized as an immunosensing platform and anti-CDH22 antibodies bound to aldehyde groups of benzaldehyde substituted poly(phosphazene) (P-PHP) covalently.	benzaldehyde	188-200	cadherin 22	Homo sapiens	143-148
30362188-5	2018	Consequently, mutants that lack gcy-28 do not approach AWCON -sensed odors and cannot associate benzaldehyde with starvation.	benzaldehyde	96-108	Receptor-type guanylate cyclase gcy-28	Caenorhabditis elegans	32-38
29253950-1	2018	The preparation, characterisation and application of two pyridine-modified chitosan derivatives (C1 and C2) containing Cu(OAc)2 adsorbed as catalysts for the conversion of benzaldehyde into 2-nitro-1-phenylethanol are described.	benzaldehyde	172-184	heterogeneous nuclear ribonucleoprotein C	Homo sapiens	97-127
29482386-3	2018	NVP BEZ-235 (BEZ) is a dual PI3K/mTOR inhibitor that has substantial anticancer effects.	benzaldehyde	4-7	mechanistic target of rapamycin kinase	Homo sapiens	33-37
29042337-10	2018	Cell functional assays, including migration assay and phosphowestern blot analysis of the mTOR and pI3K signaling pathways, revealed that the E-selectin targeted nanoparticles loaded with BEZ had a pronounced effect on inflammation-activated endothelial cells as compared to the non-targeted BEZ-loaded nanoparticles.	benzaldehyde	188-191	mechanistic target of rapamycin kinase	Homo sapiens	90-94
29042337-10	2018	Cell functional assays, including migration assay and phosphowestern blot analysis of the mTOR and pI3K signaling pathways, revealed that the E-selectin targeted nanoparticles loaded with BEZ had a pronounced effect on inflammation-activated endothelial cells as compared to the non-targeted BEZ-loaded nanoparticles.	benzaldehyde	188-191	selectin E	Homo sapiens	142-152
29042337-10	2018	Cell functional assays, including migration assay and phosphowestern blot analysis of the mTOR and pI3K signaling pathways, revealed that the E-selectin targeted nanoparticles loaded with BEZ had a pronounced effect on inflammation-activated endothelial cells as compared to the non-targeted BEZ-loaded nanoparticles.	benzaldehyde	292-295	selectin E	Homo sapiens	142-152
29464839-3	2018	For aerobic alcohol oxidation, Pd1 /CeO2 shows extremely high catalytic activity with a TOF of 6739 h-1 and satisfactory selectivity (almost 100 % for benzaldehyde), while Pd6 /CeO2 is inactive, indicating that the true active species are single Pd atoms.	benzaldehyde	151-163	programmed cell death 1	Homo sapiens	31-34
30362188-4	2018	Here, we offer a different interpretation and show that GCY-28 functions in distinct neurons to modulate two independent processes: naive attraction to AWCON -sensed odors in the AWCON neuron, and associative learning of benzaldehyde and starvation in the AIA interneurons.	benzaldehyde	221-233	Receptor-type guanylate cyclase gcy-28	Caenorhabditis elegans	56-62
29256251-2	2018	A catalytic amount of aniline as a transient directing group was efficient for the ruthenium-catalyzed ortho-C(sp2)-H alkylation of benzaldehyde with maleimide.	benzaldehyde	132-144	Sp2 transcription factor	Homo sapiens	109-114
29502118-2	2018	The present study was designed to investigate the inhibitory effects and mechanisms of benzaldehyde, vanillin, muscone, and borneol on P-glycoprotein (P-gp).	benzaldehyde	87-99	ATP binding cassette subfamily B member 1	Homo sapiens	135-149
29502118-7	2018	CONCLUSIONS: These data indicate that benzaldehyde, vanillin, muscone and borneol could effectively reverse multidrug resistance via inhibiting the P-gp function and expression pathway.	benzaldehyde	38-50	ATP binding cassette subfamily B member 1	Homo sapiens	148-152
29502118-2	2018	The present study was designed to investigate the inhibitory effects and mechanisms of benzaldehyde, vanillin, muscone, and borneol on P-glycoprotein (P-gp).	benzaldehyde	87-99	ATP binding cassette subfamily B member 1	Homo sapiens	151-155
29034432-3	2017	Herein, we report that an uncharacterized open reading frame YKL071W from S. cerevisiae encodes a novel "classical" short-chain dehydrogenase/reductase (SDR) protein with NADH-dependent enzymatic activities for reduction of furfural (FF), glycolaldehyde (GA), formaldehyde (FA), and benzaldehyde (BZA).	benzaldehyde	283-295	short-chain dehydrogenase/reductase	Saccharomyces cerevisiae S288C	116-151
29034432-3	2017	Herein, we report that an uncharacterized open reading frame YKL071W from S. cerevisiae encodes a novel "classical" short-chain dehydrogenase/reductase (SDR) protein with NADH-dependent enzymatic activities for reduction of furfural (FF), glycolaldehyde (GA), formaldehyde (FA), and benzaldehyde (BZA).	benzaldehyde	283-295	short-chain dehydrogenase/reductase	Saccharomyces cerevisiae S288C	153-156
29034432-3	2017	Herein, we report that an uncharacterized open reading frame YKL071W from S. cerevisiae encodes a novel "classical" short-chain dehydrogenase/reductase (SDR) protein with NADH-dependent enzymatic activities for reduction of furfural (FF), glycolaldehyde (GA), formaldehyde (FA), and benzaldehyde (BZA).	benzaldehyde	297-300	short-chain dehydrogenase/reductase	Saccharomyces cerevisiae S288C	116-151
29034432-3	2017	Herein, we report that an uncharacterized open reading frame YKL071W from S. cerevisiae encodes a novel "classical" short-chain dehydrogenase/reductase (SDR) protein with NADH-dependent enzymatic activities for reduction of furfural (FF), glycolaldehyde (GA), formaldehyde (FA), and benzaldehyde (BZA).	benzaldehyde	297-300	short-chain dehydrogenase/reductase	Saccharomyces cerevisiae S288C	153-156
28435458-3	2017	This nanocapsule was fabricated by encapsulating stealthy cross-linked poly(2-methacryloyloxyethyl phosphorylcholine) (PMPC) and benzaldehyde groups around the protein bovine serum albumin (BSA) followed by conjugation of doxorubicin (Dox) through a pH-responsive benzoic-imine bond.	benzaldehyde	129-141	albumin	Homo sapiens	175-188
28513914-3	2017	Proline and acid groups appended to catalytic fibers of two self-sorting hydrogelators compete for the Mannich reaction between aniline, benzaldehyde, and cyclohexanone to give low overall selectivity (anti/syn 77:23).	benzaldehyde	137-149	synemin	Homo sapiens	207-210
28456625-6	2017	In addition, a rather rare chlorinated benzaldehyde derivative, 3,5-dichloro-4-methoxybenzaldehyde isolated from the same source, was found to show potent cytotoxicity, and the chlorine atom reduced a tyrosinase inhibitory activity but enhanced cytotoxicity.	benzaldehyde	39-51	tyrosinase	Mus musculus	201-211
28006102-2	2017	Herein, we report a diverse set of ortho-C(sp2)-H functionalizations of benzaldehyde substrates using the transient directing group strategy.	benzaldehyde	72-84	Sp2 transcription factor	Homo sapiens	41-46
28125229-7	2017	Compound 2 showed a 94% conversion of benzaldehyde into (dimethoxymethyl)benzene after just 1 h of reaction, among the best results registered to date for MOF materials.	benzaldehyde	38-50	lysine acetyltransferase 8	Homo sapiens	155-158
28126723-7	2017	Ald4p, on the contrary, showed activity with benzaldehyde along with a limited range of aliphatic aldehydes.	benzaldehyde	45-57	aldehyde dehydrogenase (NADP(+)) ALD4	Saccharomyces cerevisiae S288C	0-5
28158265-6	2017	The most active compounds were conjugates of 3beta-O-acetylbetulinic acid and among them, conjugate with triazole substituted by benzaldehyde 9b was the best with IC50 of 3.3 muM and therapeutic index of 9.1.	benzaldehyde	129-141	latexin	Homo sapiens	175-178
27766585-8	2016	SSAO activity was higher in fat than in plasma, when expressed as radiolabeled benzaldehyde per milligram of protein.	benzaldehyde	79-91	amine oxidase copper containing 3	Homo sapiens	0-4
28004102-7	2016	According to Langmuir model data, maximum adsorption capacities (qm) of Fez natural clay and zeolite toward methanol (M), toluene (T) and benzaldehyde (B) at 300 K are 8, 0.89 and 3.1 mmol g-1, and 15, 1.91 and 13.9 mmol g-1 respectively.	benzaldehyde	138-150	FEZ family zinc finger 1	Homo sapiens	72-75
27844007-0	2015	A theoretical study of benzaldehyde derivatives as tyrosinase inhibitors using Ab initio calculated NQCC parameters.	benzaldehyde	23-35	tyrosinase	Homo sapiens	51-61
26538114-4	2015	Co(II) catalysed galvanostatic electrolysis of toluene at room temperature has shown that benzaldehyde was formed along with a small quantity of 3-methyl-1-hexanol.	benzaldehyde	90-102	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	0-6
29899938-3	2016	This benzaldehyde-mediated photoredox reaction proceeded smoothly with household 23 W CFL bulbs as the energy source under metal-free conditions, allowing the construction of new Csp2 -Csp2 and Csp3 -Csp2 bonds and access to important pharmacophores of broad utility using commercially available reagents.	benzaldehyde	5-17	regulator of calcineurin 2	Homo sapiens	179-183
29899938-3	2016	This benzaldehyde-mediated photoredox reaction proceeded smoothly with household 23 W CFL bulbs as the energy source under metal-free conditions, allowing the construction of new Csp2 -Csp2 and Csp3 -Csp2 bonds and access to important pharmacophores of broad utility using commercially available reagents.	benzaldehyde	5-17	regulator of calcineurin 2	Homo sapiens	185-189
29899938-3	2016	This benzaldehyde-mediated photoredox reaction proceeded smoothly with household 23 W CFL bulbs as the energy source under metal-free conditions, allowing the construction of new Csp2 -Csp2 and Csp3 -Csp2 bonds and access to important pharmacophores of broad utility using commercially available reagents.	benzaldehyde	5-17	regulator of calcineurin 2	Homo sapiens	185-189
27844007-2	2015	It can catalyze two distinct reactions of melanin synthesis and benzaldehyde derivatives, which are potential tyrosinase inhibitors.	benzaldehyde	64-76	tyrosinase	Homo sapiens	110-120
25512087-4	2015	We found that DEAB is an excellent substrate for ALDH3A1, exhibiting a Vmax/KM that exceeds that of its commonly used substrate, benzaldehyde.	benzaldehyde	129-141	aldehyde dehydrogenase 3 family member A1	Homo sapiens	49-56
26041530-0	2015	Determination of human serum semicarbazide-sensitive amine oxidase activity via flow injection analysis with fluorescence detection after online derivatization of the enzymatically produced benzaldehyde with 1,2-diaminoanthraquinone.	benzaldehyde	190-202	amine oxidase copper containing 2	Homo sapiens	29-66
26041530-2	2015	Benzaldehyde, generated by the action of SSAO after incubation of serum with benzylamine, was derivatized with a novel aromatic aldehyde-specific reagent (1,2-diaminoanthraquinone) and the fluorescent product was measured by fluorescence detection at excitation and emission wavelengths of 390 and 570nm, respectively.	benzaldehyde	0-12	amine oxidase copper containing 2	Homo sapiens	41-45
26041530-2	2015	Benzaldehyde, generated by the action of SSAO after incubation of serum with benzylamine, was derivatized with a novel aromatic aldehyde-specific reagent (1,2-diaminoanthraquinone) and the fluorescent product was measured by fluorescence detection at excitation and emission wavelengths of 390 and 570nm, respectively.	benzaldehyde	119-136	amine oxidase copper containing 2	Homo sapiens	41-45
26041530-3	2015	Serum SSAO activity was defined as benzaldehyde (nmol) formed per milliliter serum per hour.	benzaldehyde	35-47	amine oxidase copper containing 2	Homo sapiens	6-10
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.	benzaldehyde	69-81	purinergic receptor P2X 1	Homo sapiens	14-18
25587431-1	2014	Biosensors for the detection of benzaldehyde and gamma-aminobutyric acid (GABA) are reported using aldehyde oxidoreductase PaoABC from Escherichia coli immobilized in a polymer containing bound low potential osmium redox complexes.	benzaldehyde	32-44	oxidoreductase	Escherichia coli	108-122
25107441-5	2014	These results imply that oral benzaldehyde exerts antiallergic effects in murine allergic asthma and rhinitis, possibly through inhibition of HIF-1alpha and VEGF.	benzaldehyde	30-42	hypoxia inducible factor 1, alpha subunit	Mus musculus	142-152
25107441-5	2014	These results imply that oral benzaldehyde exerts antiallergic effects in murine allergic asthma and rhinitis, possibly through inhibition of HIF-1alpha and VEGF.	benzaldehyde	30-42	vascular endothelial growth factor A	Mus musculus	157-161
25050912-5	2014	Thus, benzaldehyde reacts with 6 to give the [2 + 2] cycloaddition product 7, while 4-bromoacetophenone reacts via C-H bond cleavage and formation of the enolate Cp*(IXy)(H)2RuSiH[OC( CH2)C6H4Br]Trip (8).	benzaldehyde	6-18	TRAF interacting protein	Homo sapiens	195-199
24853908-2	2014	METHODS: Plasma SSAO activity in 94 type 1 diabetes (T1DM) patients, including 34 with microvascular complications T1DM CX[+], and in 96 healthy subjects (CON) was measured by production of benzaldehyde using high-performance liquid chromatography (HPLC).	benzaldehyde	190-202	amine oxidase copper containing 3	Homo sapiens	16-20
25122208-6	2014	Our results indicated that increased CG11699 expression leads to xenobiotic stress resistance through increased ALDH-III activity: flies with FBti0019627 insertion showed increased survival rate in response to benzaldehyde, a natural xenobiotic, and to carbofuran, a synthetic insecticide.	benzaldehyde	210-222	uncharacterized protein	Drosophila melanogaster	37-44
25122208-6	2014	Our results indicated that increased CG11699 expression leads to xenobiotic stress resistance through increased ALDH-III activity: flies with FBti0019627 insertion showed increased survival rate in response to benzaldehyde, a natural xenobiotic, and to carbofuran, a synthetic insecticide.	benzaldehyde	210-222	Aldehyde dehydrogenase type III	Drosophila melanogaster	112-120
25028006-4	2014	Finally, we also validate our approach empirically by analyzing the behavior of the derivative couplings around the T1/T2 conical intersection of benzaldehyde.	benzaldehyde	146-158	interleukin 1 receptor like 1	Homo sapiens	116-121
24358880-9	2013	TRPV1 knockouts showed deficiencies in the detection of benzaldehyde, cyclohexanone and eugenol in at least one assay.	benzaldehyde	56-68	transient receptor potential cation channel, subfamily V, member 1	Mus musculus	0-5
23551266-1	2013	Treatment of benzaldehyde and an acetoacetate ester with potassium carbonate in an alcohol solvent proceeds via gamma-C-alkylation rather than alpha-C-alkylation resulting in the formation of 6-phenyl-2,4-dioxotetrahydropyran.	benzaldehyde	13-25	interleukin 2 receptor subunit gamma	Homo sapiens	112-119
23914541-3	2013	The health risks of PCO of toluene and benzaldehyde were assessed based on health risk influence index (eta).	benzaldehyde	39-51	endothelin receptor type A	Homo sapiens	104-107
24061865-1	2013	PURPOSE: Benzaldehyde dimethane sulfonate (DMS612, NSC281612, BEN) is an alkylator with activity against renal cell carcinoma, currently in phase I trials.	benzaldehyde	9-21	general transcription factor II I repeat domain-containing 1	Mus musculus	62-65
23914541-7	2013	In the PCO process of toluene and benzaldehyde, eta reached the maximum values of 8 499.68 and 21.43, with the eta(VAs), contribution of VAs to the health risk influence index of outlet, reaching 99.3% and 98.3%, respectively.	benzaldehyde	34-46	endothelin receptor type A	Homo sapiens	48-51
23914541-7	2013	In the PCO process of toluene and benzaldehyde, eta reached the maximum values of 8 499.68 and 21.43, with the eta(VAs), contribution of VAs to the health risk influence index of outlet, reaching 99.3% and 98.3%, respectively.	benzaldehyde	34-46	endothelin receptor type A	Homo sapiens	111-114
23914541-9	2013	When PCO of toluene and benzaldehyde reached steady state, eta were 236.09 and 2.30, and eta(VAs) reached 97.9% and 97.8%, respectively.	benzaldehyde	24-36	endothelin receptor type A	Homo sapiens	59-62
23285706-10	2012	Kinetic parameters (Km, Vmax) of recombinant ALDH1A1 towards several aliphatic and aromatic aldehydes occurring in food products (vanillin, citral, furfural, cinnamaldehyde, anisaldehyde, benzaldehyde and trans-hexenal) were determined by measuring the increase of NADH fluorescence after adding various concentrations of aldehyde substrates.	benzaldehyde	188-200	aldehyde dehydrogenase 1 family member A1	Homo sapiens	45-52
22051410-2	2012	The density functional theory (DFT) B3LYP/6-31G* method was chosen to calculate the infrared spectrum of benzaldehyde in gaseous state.	benzaldehyde	105-117	protein tyrosine phosphatase non-receptor type 22	Homo sapiens	38-41
22279051-3	2012	AO has an important role in the metabolism of drugs based on its broad substrate specificity oxidizing aromatic aza-heterocycles, for example, N(1)-methylnicotinamide and N-methylphthalazinium, or aldehydes, such as benzaldehyde, retinal, and vanillin.	benzaldehyde	216-228	aldehyde oxidase 1	Homo sapiens	0-2
22154910-8	2012	The superior photocatalytic activity of SiO(2)@CdS composites for the benzaldehyde oxidation under UV irradiation has been displayed.	benzaldehyde	70-82	CDP-diacylglycerol synthase 1	Homo sapiens	47-50
21893110-0	2011	Ultra-high olfactory sensitivity for the human sperm-attractant aromatic aldehyde bourgeonal in CD-1 mice.	benzaldehyde	64-81	CD1c molecule	Homo sapiens	96-100
23209525-3	2012	The relative configuration of a new isomer of tropinone aldol accessible synthetically through the direct solventless reaction of tropinone and benzaldehyde in the presence of water was determined as exo,syn by comparison of NMR data of the aldol isomers, in particular vicinal coupling constants and shifts corresponding to the side-chain CH group, with data of related TBDMS derivatives and confirmed by single-crystal X-ray diffraction.	benzaldehyde	144-156	synemin	Homo sapiens	73-76
21414430-6	2011	The metabolites of BZA or MA catalyzed by SSAO, hydrogen peroxide, formaldehyde, and benzaldehyde could also significantly decrease LPS-induced nitric oxide and TNF-alpha production, iNOS and COX-2 expression, and glucose consumption in vitro.	benzaldehyde	85-97	tumor necrosis factor	Mus musculus	161-170
21705476-1	2011	Aldehyde oxidase (AOX) is characterized by a broad substrate specificity, oxidizing aromatic azaheterocycles, such as N1-methylnicotinamide and N-methylphthalazinium, or aldehydes, such as benzaldehyde, retinal, and vanillin.	benzaldehyde	189-201	acyl-Coenzyme A oxidase 1, palmitoyl	Mus musculus	0-16
21705476-1	2011	Aldehyde oxidase (AOX) is characterized by a broad substrate specificity, oxidizing aromatic azaheterocycles, such as N1-methylnicotinamide and N-methylphthalazinium, or aldehydes, such as benzaldehyde, retinal, and vanillin.	benzaldehyde	189-201	acyl-Coenzyme A oxidase 1, palmitoyl	Mus musculus	18-21
21414430-6	2011	The metabolites of BZA or MA catalyzed by SSAO, hydrogen peroxide, formaldehyde, and benzaldehyde could also significantly decrease LPS-induced nitric oxide and TNF-alpha production, iNOS and COX-2 expression, and glucose consumption in vitro.	benzaldehyde	85-97	nitric oxide synthase 2, inducible	Mus musculus	183-187
21414430-6	2011	The metabolites of BZA or MA catalyzed by SSAO, hydrogen peroxide, formaldehyde, and benzaldehyde could also significantly decrease LPS-induced nitric oxide and TNF-alpha production, iNOS and COX-2 expression, and glucose consumption in vitro.	benzaldehyde	85-97	cytochrome c oxidase II, mitochondrial	Mus musculus	192-197
21508382-6	2011	RESULTS: The sulfated chitosan (SCS) and the sulfated benzaldehyde chitosan (SBCS) significantly inhibited cell proliferation, induced apoptosis and blocked the FGF-2-induced phosphorylation of ERK in MCF-7 cells, SBCS had better inhibitory effects and a lower IC(50) compared to SCS.	benzaldehyde	54-66	fibroblast growth factor 2	Homo sapiens	161-166
20699116-5	2010	ALDH3B1 demonstrated high affinity for hexanal (K(m)=62 muM), octanal (K(m)=8 muM), 4-hydroxy-2-nonenal (4HNE; K(m)=52 muM), and benzaldehyde (K(m)=46 muM).	benzaldehyde	129-141	aldehyde dehydrogenase 3 family member B1	Homo sapiens	0-7
21508382-6	2011	RESULTS: The sulfated chitosan (SCS) and the sulfated benzaldehyde chitosan (SBCS) significantly inhibited cell proliferation, induced apoptosis and blocked the FGF-2-induced phosphorylation of ERK in MCF-7 cells, SBCS had better inhibitory effects and a lower IC(50) compared to SCS.	benzaldehyde	54-66	mitogen-activated protein kinase 1	Homo sapiens	194-197
21308960-6	2011	Benzaldehyde (9 microg mL(-1) ) was the most toxic compound, followed by gamma-eudesmol (50 microg mL(-1) ) and estragole (180 microg mL(-1) ), based on 96 h EC(50) values.	benzaldehyde	0-12	L1 cell adhesion molecule	Mus musculus	23-29
20833259-7	2010	Kvbeta2 was found to catalyse the reduction of aromatic aldehyde substrates such as 2, 3 and 4-nitrobenzaldehydes, 4-hydroxybenzaldehyde, pyridine 2-aldehyde and benzaldehyde.	benzaldehyde	47-64	potassium voltage-gated channel subfamily A regulatory beta subunit 2	Homo sapiens	0-7
20833259-7	2010	Kvbeta2 was found to catalyse the reduction of aromatic aldehyde substrates such as 2, 3 and 4-nitrobenzaldehydes, 4-hydroxybenzaldehyde, pyridine 2-aldehyde and benzaldehyde.	benzaldehyde	100-112	potassium voltage-gated channel subfamily A regulatory beta subunit 2	Homo sapiens	0-7
20835425-1	2010	Transketolase mutants have been identified that accept aromatic acceptors with good stereoselectivities, in particular benzaldehyde for which the wild type enzyme showed no activity.	benzaldehyde	119-131	transketolase	Homo sapiens	0-13
21043489-2	2010	By combining the surface basicity and semiconductor functions of mpg-C(3)N(4), the photocatalytic system can realize a high catalytic selectivity to generate benzaldehyde.	benzaldehyde	158-170	N-methylpurine DNA glycosylase	Homo sapiens	65-68
20503998-1	2010	The origin of stereoselective formation of Evans syn and non-Evans anti aldol products in the reaction between titanium enolate derived from N-succinyloxazolidinone and benzaldehyde is established by using transition-state modeling.	benzaldehyde	169-181	synemin	Homo sapiens	49-52
20628035-5	2010	We identified polymorphisms in Or10a, Or43a, and Or67b that were significantly associated with variation in response to benzaldehyde.	benzaldehyde	120-132	Odorant receptor 10a	Drosophila melanogaster	31-36
20628035-5	2010	We identified polymorphisms in Or10a, Or43a, and Or67b that were significantly associated with variation in response to benzaldehyde.	benzaldehyde	120-132	Odorant receptor 43a	Drosophila melanogaster	38-43
20628035-5	2010	We identified polymorphisms in Or10a, Or43a, and Or67b that were significantly associated with variation in response to benzaldehyde.	benzaldehyde	120-132	Odorant receptor 67b	Drosophila melanogaster	49-54
20628035-9	2010	We also observed a correspondence between behavioral response to benzaldehyde and differences in Or10a and Or43a expression.	benzaldehyde	65-77	Odorant receptor 10a	Drosophila melanogaster	97-102
20628035-9	2010	We also observed a correspondence between behavioral response to benzaldehyde and differences in Or10a and Or43a expression.	benzaldehyde	65-77	Odorant receptor 43a	Drosophila melanogaster	107-112
20432412-0	2010	Synthesis of benzaldehyde-functionalized glycans: a novel approach towards glyco-SAMs as a tool for surface plasmon resonance studies.	benzaldehyde	13-25	methionine adenosyltransferase 1A	Homo sapiens	81-85
19936267-5	2009	In the course of this study, an L-asparagine derivative was condensed with benzaldehyde and subsequently converted to orthogonally protected (R)-beta(2)-homoaspartate.	benzaldehyde	75-87	potassium calcium-activated channel subfamily M regulatory beta subunit 2	Homo sapiens	145-151
20378596-1	2010	Recent studies have shown that sperm chemotaxis critically involves the human olfactory receptor OR1D2, which is activated by the aromatic aldehyde bourgeonal.	benzaldehyde	130-147	olfactory receptor family 1 subfamily D member 2	Homo sapiens	97-102
20045461-2	2010	In mammals, benzylamine is metabolized by semicarbazide-sensitive amine oxidase (SSAO) to benzaldehyde and hydrogen peroxide.	benzaldehyde	90-102	amine oxidase, copper containing 3	Mus musculus	42-79
20045461-2	2010	In mammals, benzylamine is metabolized by semicarbazide-sensitive amine oxidase (SSAO) to benzaldehyde and hydrogen peroxide.	benzaldehyde	90-102	amine oxidase, copper containing 3	Mus musculus	81-85
19945871-2	2010	SAR studies, by varying the substituted benzaldehyde components, lead to the discovery of a series of potent JAK2 kinase inhibitors.	benzaldehyde	40-52	Janus kinase 2	Homo sapiens	109-113
20042251-8	2010	Benzaldehyde-functionalized glycosides of mono and disaccharides were synthesized by metathesis and could be used for the formation of novel glyco-self assembled monolayers (glyco-SAMs) employing various tether structures and attached to gold surfaces.	benzaldehyde	0-12	methionine adenosyltransferase 1A	Homo sapiens	180-184
20534848-2	2010	Here, we show that insulin signaling also is required in benzaldehyde-starvation associative plasticity, in which worms pre-exposed to the odor attractant benzaldehyde in the absence of food subsequently demonstrate a conditioned aversion response toward the odorant.	benzaldehyde	57-69	insulin	Homo sapiens	19-26
20534848-2	2010	Here, we show that insulin signaling also is required in benzaldehyde-starvation associative plasticity, in which worms pre-exposed to the odor attractant benzaldehyde in the absence of food subsequently demonstrate a conditioned aversion response toward the odorant.	benzaldehyde	155-167	insulin	Homo sapiens	19-26
20534848-3	2010	Animals with mutations in insulin-related 1 (ins-1), abnormal dauer formation 2 (daf-2), and aging alteration 1 (age-1), which encode the homolog of human insulin, insulin/IGF-1 receptor, and PIP3 kinase, respectively, demonstrated significant deficits in benzaldehyde-starvation associative plasticity.	benzaldehyde	256-268	insulin	Homo sapiens	155-186
19156319-3	2009	Furthermore, the aldol reaction of the lithium enolate of cis-2-ferrocenyl-3-pivaloyl-4-methyl-1,3-oxazolidin-5-one with benzaldehyde followed by in situ O-protection affords O-protected aldol products in >98% de, with hydrolysis affording (2R,3S)-2-amino-2-methyl-3-hydroxy-3-phenylpropanoic acid in >98% de.	benzaldehyde	121-133	suppressor of cytokine signaling 2	Homo sapiens	58-63
19297586-0	2009	An aldehyde oxidase in developing seeds of Arabidopsis converts benzaldehyde to benzoic Acid.	benzaldehyde	64-76	aldehyde oxidase 1	Arabidopsis thaliana	3-19
18983993-15	2009	Yeast ALDH2 exhibited K(M) for straight-chain aliphatic aldehydes (C1-C10), 2.3-210 microM, and substrate inhibition constants (C2-C10), 79-2900 microM, with a trend of being smaller K(M) and K(i) for longer chain lengths; and K(M) for cinnamaldehyde, benzaldehyde, and 2-furaldehyde, 5.0, 79, and 1000 microM, respectively.	benzaldehyde	252-264	aldehyde dehydrogenase 2 family member	Homo sapiens	6-11
19730689-4	2009	We demonstrate that the inositol 1,4,5-trisphosphate receptor (IP(3)R), encoded by itr-1, functions in the reversal responses to nose touch and benzaldehyde, but not in other known ASH-mediated responses.	benzaldehyde	144-156	Inositol 1,4,5-trisphosphate receptor itr-1	Caenorhabditis elegans	83-88
19200549-7	2009	A cyclohexyldiol-silica fiber was used, as a simple example of applicability, for the successful determination of benzaldehyde, acetophenone and dimethylphenol at trace level in spiked tap water.	benzaldehyde	114-126	nuclear RNA export factor 1	Homo sapiens	185-188
19100833-7	2009	BmOR19 responds to linalool, while BmOR45 and BmOR47 respond to benzoic acid > 2-phenylethanol > benzaldehyde.	benzaldehyde	103-115	olfactory receptor 45	Bombyx mori	35-41
19100833-7	2009	BmOR19 responds to linalool, while BmOR45 and BmOR47 respond to benzoic acid > 2-phenylethanol > benzaldehyde.	benzaldehyde	103-115	olfactory receptor 47	Bombyx mori	46-52
18522428-1	2008	Theoretical simulation on the enantioselective cyanation of benzaldehyde over titanium-salicylaldehyde catalysts is performed with B3LYP//ONIOM methods.	benzaldehyde	60-72	protein tyrosine phosphatase non-receptor type 22	Homo sapiens	133-136
18984566-4	2008	This delayed avoidance is due to an increased attraction rather than a decreased avoidance to benzaldehyde because (1) aged odr-3 mutants that are defective in odor attraction showed no delayed benzaldehyde avoidance, and (2) the delay in avoidance was also observed with another attractant diacetyl, but not the repellent octanol.	benzaldehyde	94-106	Guanine nucleotide-binding protein alpha-17 subunit	Caenorhabditis elegans	124-129
18186090-4	2008	Analysis by solid-phase catalysis/circular dichroism high-throughput screening of a copper-catalyzed Henry reaction revealed that ligand L25, comprising a (S,S)-diphenylethylenediamine-derived imidazoline, (S)-phenylethylamine, and dibromophenol, was highly efficient, thus providing the adduct of nitromethane and benzaldehyde in 95 % ee.	benzaldehyde	315-327	immunoglobulin kappa variable 3D-7	Homo sapiens	137-140
21202829-3	2008	The title product resulted from a three-component reaction of benzaldehyde, 1-ethynylbenzene and p-toluidine via C-H activation of 1-ethynylbenzene catalyzed by CuI in the ionic liquid 1-butyl-3-methyl-imidazolium hexa-fluoro-phosphate.	benzaldehyde	62-74	hexosaminidase subunit alpha	Homo sapiens	214-218
18154299-2	2008	A 80% de in favor of the anti product has been experimentally observed with both saturated aldehydes, while for benzaldehyde, a 1:1 syn/anti ratio has been found.	benzaldehyde	112-124	synemin	Homo sapiens	132-135
18154299-5	2008	The computational investigation of the reaction of these allylic organozinc complexes with benzaldehyde and 2-methylpropanal demonstrates in both cases the existence of two competitive reaction paths leading to the syn and anti adducts, respectively.	benzaldehyde	91-103	synemin	Homo sapiens	215-218
17867698-1	2007	syn-beta-Hydroxyallylsilanes of general structure 11 and 28 are prepared in 50-86% yield and 91-95% ee (for aliphatic aldehydes; 50% ee for benzaldehyde) via the BF(3).Et(2)O-promoted gamma-silylallylboration reactions, using reagents 14 and 15.	benzaldehyde	140-152	synemin	Homo sapiens	0-3
19148285-1	2008	The palladium (II) bis-chelate Pd (L(1-3))(2) and platinum (II) tetranuclear Pt(4)(L(4))(4) complexes of benzaldehyde thiosemicarbazone derivatives have been synthesized, and characterized by elemental analysis and IR, FAB(+)-mass and NMR ((1)H, (13)C) spectroscopy.	benzaldehyde	105-117	FA complementation group B	Homo sapiens	219-222
18061070-5	2007	The ALDH-2 activity and expression in these segments were assessed by the conversion of a benzaldehyde or its derivative to the benzoic acid metabolite and by Western blotting technique.	benzaldehyde	90-102	aldehyde dehydrogenase 2 family member	Homo sapiens	4-10
17720903-6	2007	Four polymorphisms in 3 Obp genes exceeded the statistical permutation threshold for association with responsiveness to benzaldehyde, suggesting redundancy and/or combinatorial recognition by these OBPs of this odorant.	benzaldehyde	120-132	Optix-binding protein	Drosophila melanogaster	24-27
17382292-5	2007	Human ALDH3B1 was baculovirus-expressed and found to be catalytically active towards medium- and long-chain aliphatic aldehydes and the aromatic aldehyde benzaldehyde.	benzaldehyde	136-153	aldehyde dehydrogenase 3 family member B1	Homo sapiens	6-13
17435226-3	2007	To begin to address this problem, we used olfactory behavior in Drosophila melanogaster as a model and showed that a hypomorphic transposon-mediated mutation of the early developmental gene Semaphorin-5c (Sema-5c) results in aberrant behavioral responses to the repellant odorant benzaldehyde.	benzaldehyde	280-292	Semaphorin 5c	Drosophila melanogaster	190-203
17435226-3	2007	To begin to address this problem, we used olfactory behavior in Drosophila melanogaster as a model and showed that a hypomorphic transposon-mediated mutation of the early developmental gene Semaphorin-5c (Sema-5c) results in aberrant behavioral responses to the repellant odorant benzaldehyde.	benzaldehyde	280-292	Semaphorin 5c	Drosophila melanogaster	205-212
17382292-5	2007	Human ALDH3B1 was baculovirus-expressed and found to be catalytically active towards medium- and long-chain aliphatic aldehydes and the aromatic aldehyde benzaldehyde.	benzaldehyde	154-166	aldehyde dehydrogenase 3 family member B1	Homo sapiens	6-13
17249797-1	2007	[reaction: see text] The alcohol-catalyzed Diels-Alder reactions of acrolein and benzaldehyde with Rawal"s diene were evaluated with density functional theory (B3LYP/6-31G(d)).	benzaldehyde	81-93	protein tyrosine phosphatase non-receptor type 22	Homo sapiens	162-165
17318518-2	2007	The functional sensing surface was fabricated by the immobilization of a benzaldehyde-ovalbumin conjugate (BZ-OVA) on Au-thiolate SAMs containing carboxyl end groups.	benzaldehyde	73-85	methionine adenosyltransferase 1A	Homo sapiens	130-134
16354669-6	2006	PAO supplemented with benzaldehyde predominantly catalyzed the cleavage of (R)-isomer of alpha-methylspermidine, whereas in the presence of pyridoxal the (S)-alpha-methylspermidine was preferred.	benzaldehyde	22-34	polyamine oxidase	Homo sapiens	0-3
16802822-3	2006	The reaction proceeds smoothly at room temperature in the absence of any phosphane or nitrogen ligands and is highly regioselective and stereoselective for a wide variety combination of aldehydes and 1,3-dienes: e.g., isoprene and benzaldehyde combine to give a mixture of anti- and syn-1-phenyl-3-methyl-4-penten-1-ol (2.2) in a ratio of 15:1 in 90% yield.	benzaldehyde	231-243	synapsin I	Homo sapiens	283-288
15958189-1	2005	Acetohydroxy acid synthase (AHAS) and related enzymes catalyze the production of chiral compounds [(S)-acetolactate, (S)-acetohydroxybutyrate, or (R)-phenylacetylcarbinol] from achiral substrates (pyruvate, 2-ketobutyrate, or benzaldehyde).	benzaldehyde	226-238	ilvB acetolactate synthase like	Homo sapiens	0-26
16441137-1	2006	The benzaldehyde thiosemicarbazones are found to undergo oxidation at the sulfur center upon reaction with [Rh(PPh3)3Cl] in refluxing ethanol in the presence of a base (NEt3).	benzaldehyde	4-16	protein phosphatase 4 catalytic subunit	Homo sapiens	111-115
16441137-1	2006	The benzaldehyde thiosemicarbazones are found to undergo oxidation at the sulfur center upon reaction with [Rh(PPh3)3Cl] in refluxing ethanol in the presence of a base (NEt3).	benzaldehyde	4-16	tetraspanin 2	Homo sapiens	169-173
16441137-4	2006	Reaction of the benzaldehyde thiosemicarbazones with [Rh(PPh3)3Cl] in refluxing ethanol in the absence of NEt3 affords another group of organorhodium complexes, in which the thiosemicarbazones are coordinated to rhodium as tridentate CNS donors, along with two triphenylphosphines and a chloride.	benzaldehyde	16-28	protein phosphatase 4 catalytic subunit	Homo sapiens	57-61
16188506-3	2005	SSAO activity can be quantified by assaying benzaldehyde production using fluorescent derivatisation and separation by HPLC.	benzaldehyde	44-56	amine oxidase copper containing 2	Homo sapiens	0-4
15958189-1	2005	Acetohydroxy acid synthase (AHAS) and related enzymes catalyze the production of chiral compounds [(S)-acetolactate, (S)-acetohydroxybutyrate, or (R)-phenylacetylcarbinol] from achiral substrates (pyruvate, 2-ketobutyrate, or benzaldehyde).	benzaldehyde	226-238	ilvB acetolactate synthase like	Homo sapiens	28-32
15380725-7	2004	SSAO enzyme activity is defined as benzaldehyde (nmol) formed per ml plasma per hour.	benzaldehyde	35-47	amine oxidase copper containing 2	Homo sapiens	0-4
16833774-0	2005	Hydrogenation of benzaldehyde and cinnamaldehyde in compressed CO2 medium with a Pt/C catalyst: a study on molecular interactions and pressure effects.	benzaldehyde	17-29	complement C2	Homo sapiens	63-66
15720138-5	2005	First, classical AOX electron donor substrates (benzaldehyde, 2-hydroxypyrimidine, and N-methylnicotinamide) dramatically increase the rate of formation of IMI metabolites.	benzaldehyde	48-60	aldehyde oxidase 1	Homo sapiens	17-20
15647466-0	2005	An increased receptive field of olfactory receptor Or43a in the antennal lobe of Drosophila reduces benzaldehyde-driven avoidance behavior.	benzaldehyde	100-112	Odorant receptor 43a	Drosophila melanogaster	51-56
15647466-3	2005	The behavioral response of GH320/UAS-or43a flies was changed upon benzaldehyde application.	benzaldehyde	66-78	Odorant receptor 43a	Drosophila melanogaster	37-42
15647466-6	2005	We therefore conclude that the application of benzaldehyde, an identified ligand of Or43a, resulted in activation of a number of glomeruli in transformed flies in addition to glomerulus DA4, which is the regular target of Or43a expressing neurons.	benzaldehyde	46-58	Odorant receptor 43a	Drosophila melanogaster	84-89
15647466-6	2005	We therefore conclude that the application of benzaldehyde, an identified ligand of Or43a, resulted in activation of a number of glomeruli in transformed flies in addition to glomerulus DA4, which is the regular target of Or43a expressing neurons.	benzaldehyde	46-58	Odorant receptor 43a	Drosophila melanogaster	222-227
15390260-2	2004	We have utilized molecular mechanics (MM) simulations, in conjunction with new force field parameters for aldehydes, to study the atomic details of benzaldehyde binding to ALDH3A1.	benzaldehyde	148-160	aldehyde dehydrogenase 3 family member A1	Homo sapiens	172-179
15390260-4	2004	The negatively charged Cys243 (thiolate form) of ALDH3A1 also binds benzaldehyde in a stable conformation but in this complex the sulfur of Cys243 is oriented away from benzaldehyde yet yields the most favorable MM-GBMV complexation energy.	benzaldehyde	68-80	aldehyde dehydrogenase 3 family member A1	Homo sapiens	49-56
15390260-4	2004	The negatively charged Cys243 (thiolate form) of ALDH3A1 also binds benzaldehyde in a stable conformation but in this complex the sulfur of Cys243 is oriented away from benzaldehyde yet yields the most favorable MM-GBMV complexation energy.	benzaldehyde	169-181	aldehyde dehydrogenase 3 family member A1	Homo sapiens	49-56
15200326-2	2004	The enolate can be protonated to yield the corresponding ketone or treated with benzaldehyde to give the aldol product with good syn or anti diastereoselectivity depending on the conditions.	benzaldehyde	80-92	synemin	Homo sapiens	129-132
15255735-5	2004	Another distinct behavior between the Ni- and Pd-catalyzed allylation was demonstrated in the reaction of hex-1,5-diene-3,4-diol derivatives: the Pd catalyst did not give any coupling product, whereas the Ni-catalyzed InI-mediated reaction with benzaldehyde afforded the 1:1 and 1:2 adduct diols selectively depending on the reaction conditions.	benzaldehyde	245-257	exonuclease 1	Homo sapiens	106-111
15255735-5	2004	Another distinct behavior between the Ni- and Pd-catalyzed allylation was demonstrated in the reaction of hex-1,5-diene-3,4-diol derivatives: the Pd catalyst did not give any coupling product, whereas the Ni-catalyzed InI-mediated reaction with benzaldehyde afforded the 1:1 and 1:2 adduct diols selectively depending on the reaction conditions.	benzaldehyde	245-257	PHD finger protein 5A	Homo sapiens	218-221
14510556-5	2003	This ligand (10 mol %) catalyzed the addition of Me2Zn to 2-naphthaldehyde, benzaldehyde, and 4-chlorobenzaldehyde to give the corresponding alcohol products in 86%, 84% and 81% ee, respectively.	benzaldehyde	76-88	malic enzyme 2	Homo sapiens	49-52
15087594-5	2004	Toluene and phenol, which compose cigarette smoke, and benzaldehyde stimulated MMP-1 and/or elastin expression.	benzaldehyde	55-67	matrix metallopeptidase 1	Homo sapiens	79-84
15087594-5	2004	Toluene and phenol, which compose cigarette smoke, and benzaldehyde stimulated MMP-1 and/or elastin expression.	benzaldehyde	55-67	elastin	Homo sapiens	92-99
15087594-7	2004	Toluene, benzaldehyde and phenol can directly cause facial wrinkling and impaired structural integrity by upregulating MMP-1 and/or elastin.	benzaldehyde	9-21	matrix metallopeptidase 1	Homo sapiens	119-124
15087594-7	2004	Toluene, benzaldehyde and phenol can directly cause facial wrinkling and impaired structural integrity by upregulating MMP-1 and/or elastin.	benzaldehyde	9-21	elastin	Homo sapiens	132-139
12693212-11	2003	of 6b with acetone forms the methyl enolate complex [Ru2(trpy)2(6,6"-Me2dppz)(CH2COCH3)](PF6)2 (9b) while, analogously to a Cannizarro reaction, the reaction with benzaldehyde forms the bridging benzoate complex [Ru2(trpy)2(6,6"-Me2dppz)(C6H4CO2)](PF6)2 (11b).	benzaldehyde	163-175	sperm associated antigen 17	Homo sapiens	89-92
12767028-8	2003	Sensory input to DL2 and, to a minor extent, VM1 and/or VM4, appear to be required for benzaldehyde perception, while acetone is processed through DL1.	benzaldehyde	87-99	lectin-37Da	Drosophila melanogaster	17-20
12767028-8	2003	Sensory input to DL2 and, to a minor extent, VM1 and/or VM4, appear to be required for benzaldehyde perception, while acetone is processed through DL1.	benzaldehyde	87-99	vm1	Drosophila melanogaster	45-48
12767029-8	2003	Exposure to benzaldehyde at days 2-5 of adult life, but not at 8-11, causes behavioral adaptation as well as structural changes in DM2 and V glomeruli.	benzaldehyde	12-24	tarsal-less 2A	Drosophila melanogaster	131-134
12746108-0	2003	More potent inhibition of human CYP2A6 than mouse CYP2A5 enzyme activities by derivatives of phenylethylamine and benzaldehyde.	benzaldehyde	114-126	cytochrome P450 family 2 subfamily A member 6	Homo sapiens	32-38
12746108-0	2003	More potent inhibition of human CYP2A6 than mouse CYP2A5 enzyme activities by derivatives of phenylethylamine and benzaldehyde.	benzaldehyde	114-126	cytochrome P450, family 2, subfamily a, polypeptide 5	Mus musculus	50-56
12746108-4	2003	The method was used to test inhibition of human and mouse CYP2A enzymes by three phenylethylamine derivatives 2-(p-tolyl)-ethylamine, amphetamine, 2-phenylethylamine and benzaldehyde, and two of its derivatives, 4-methylbenzaldehyde and 4-methoxybenzaldehyde.	benzaldehyde	170-182	cytochrome P450, family 2, subfamily a	Mus musculus	58-63
12746108-6	2003	The benzaldehyde derivatives were more potent inhibitors of CYP2A5 than the phenylethylamines.	benzaldehyde	4-16	cytochrome P450, family 2, subfamily a, polypeptide 5	Mus musculus	60-66
12746108-9	2003	Amphetamine is a weak inhibitor of CYP2A6, whereas benzaldehyde is a suicide inhibitor with K(inact) = 0.16 min(-1) and K(I) = 18 micro M. The K(ic) values of 2-phenylethylamine, 2-(p-tolyl)-ethylamine, 4-methylbenzaldehyde and 4-methoxybenzaldehyde were 1.13, 0.23, 0.36 and 0.73 micro M for CYP2A6, respectively.	benzaldehyde	51-63	cytochrome P450 family 2 subfamily A member 6	Homo sapiens	293-299
12590526-2	2003	For instance, the reaction of trimethylsilyl nitronate 2 (R(1) = Me) with benzaldehyde (R(2) = Ph) in THF in the presence of (S,S)-1 (2 mol %) proceeded smoothly at -78 degrees C, giving the corresponding nitroaldol adduct 3 (R(1) = Me, R(2) = Ph) in 92% isolated yield (anti/syn = 92:8) with 95% ee (anti isomer).	benzaldehyde	74-86	synemin	Homo sapiens	276-279
12105956-6	2002	Using this technique benzaldehyde and vanillin were observed to bind with bovine serum albumin, whereas 2-phenylethanol was identified as a nonbinding or weakly binding ligand with BSA.	benzaldehyde	21-33	albumin	Homo sapiens	81-94
12196396-7	2002	Behavioral assays show that a threefold decrease in DSC1 mRNA is accompanied by a threefold shift in the dose response for avoidance of the repellent odorant, benzaldehyde, toward higher odorant concentrations.	benzaldehyde	159-171	Na channel protein 60E	Drosophila melanogaster	52-56
11855704-4	2002	The immobilized TADDOLs were titanated to give (iPrO)2Ti-, Cl2Ti-, or (TosO)2Ti-TADDOLates which were used for catalyzing the additions of Et2Zn or Bu2Zn to PhCHO and of diphenyl nitrone to 3-crotonoyl-oxazolidinone.	benzaldehyde	157-162	Fc mu receptor	Homo sapiens	71-75
12047152-2	2002	Treatment of these substrates with TpRu(PPh3)(CH3CN)2PF6 (8.0 mol %) catalyst in 1,2-dichloroethane (80 degrees C, 12 h) afforded functionalized 1,3-dienes and benzyl aldehyde in good yields.	benzaldehyde	160-175	caveolin 1	Homo sapiens	40-44
12036350-7	2002	We describe herein the rational design and synthesis of a class of imine conjugates produced by coupling amino acids to a range of benzaldehyde derivatives that inhibit MIF tautomerase and biological activities.	benzaldehyde	131-143	macrophage migration inhibitory factor	Homo sapiens	169-172
12036350-14	2002	The inhibitory activity of amino acid-benzaldehyde Schiff base-type MIF antagonists is the first step toward a meaningful structure/function analysis of inhibitors of MIF cellular bioactivities.	benzaldehyde	38-50	macrophage migration inhibitory factor	Homo sapiens	68-71
12036350-14	2002	The inhibitory activity of amino acid-benzaldehyde Schiff base-type MIF antagonists is the first step toward a meaningful structure/function analysis of inhibitors of MIF cellular bioactivities.	benzaldehyde	38-50	macrophage migration inhibitory factor	Homo sapiens	167-170
11487650-7	2001	Of a sample of eight glomeruli measured, dorsal medial (DM) 2 and ventral (V) were affected by benzaldehyde exposure, whereas DM6 was affected by isoamyl acetate.	benzaldehyde	95-107	tarsal-less 2A	Drosophila melanogaster	41-61
11569919-4	2001	Cytosolic AO was characterised using both the metabolism of N-[(2-dimethylamino)ethyl] acridine-4-carboxamide (DACA) and benzaldehyde to form DACA-9(10H)-acridone (quantified by HPLC with fluorescence detection) and benzoic acid (quantified spectrophotometrically).	benzaldehyde	121-133	aldehyde oxidase 1	Homo sapiens	10-12
11481495-5	2001	Electroantennogram recordings from transformed and wild-type flies were used to identify cyclohexanol, cyclohexanone, benzaldehyde, and benzyl alcohol as ligands for the Or43a.	benzaldehyde	118-130	Odorant receptor 43a	Drosophila melanogaster	170-175
11425590-0	2001	Hydroxy- or methoxy-substituted benzaldoximes and benzaldehyde-O-alkyloximes as tyrosinase inhibitors.	benzaldehyde	50-62	tyrosinase	Homo sapiens	80-90
11456132-2	2001	Monkey liver cytosol exhibited significant reductase activities toward zonisamide, sulindac and imipramine N-oxide in the presence of 2-hydroxypyrimidine or benzaldehyde, an electron donor to aldehyde oxidase.	benzaldehyde	157-169	aldehyde oxidase 1	Homo sapiens	192-208
11073254-2	2000	Since the addition of the photoexcited benzaldehyde at the unsaturated heterocycle proceeds in a syn fashion, the benzyl group at C-2 and the hydroxy group at C-3 of the product are cis oriented.	benzaldehyde	39-51	complement C2	Homo sapiens	130-133
11306050-12	2001	Paradoxically, cells expressing ALDH3A1 were 1.5-fold more sensitive to benzaldehyde toxicity than control V79 cells.	benzaldehyde	72-84	aldehyde dehydrogenase, dimeric NADP-preferring	Cricetulus griseus	32-39
11306037-3	2001	Chloramphenicol which also elutes the enzyme from the affinity column, shows a discriminatory effect by inhibiting the ALDH1 oxidation of benzaldehyde and activating that of propionaldehyde while showing no effect when assayed with hexanal or cyclohexane-carboxaldehyde.	benzaldehyde	138-150	aldehyde dehydrogenase 1 family member A1	Homo sapiens	119-124
11306044-4	2001	Finally, our quantum mechanical model of benzaldehyde in the active site of ALDH demonstrates that the enzyme requires only minor conformational changes to be poised for nucleophilic attack on the substrate.	benzaldehyde	41-53	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	76-80
11306045-8	2001	Four hours after treatment with 25 microM ATEM, ALDH activity using benzaldehyde or propionaldehyde in hepatoma cells was decreased by 40% and cell number by 15% compared with controls.	benzaldehyde	68-80	aldehyde dehydrogenase 2 family member	Rattus norvegicus	48-52
11073254-2	2000	Since the addition of the photoexcited benzaldehyde at the unsaturated heterocycle proceeds in a syn fashion, the benzyl group at C-2 and the hydroxy group at C-3 of the product are cis oriented.	benzaldehyde	39-51	complement C3	Homo sapiens	159-162
10956534-0	2000	Kinetic investigations of product inhibition in the amino alcohol-catalyzed asymmetric alkylation of benzaldehyde with diethylzinc In situ reaction rate measurements help to define the role of product inhibition in the asymmetric alkylation of benzaldehyde with diethylzinc using (-)-MIB as a chiral reagent.	benzaldehyde	101-113	MIB E3 ubiquitin protein ligase 1	Homo sapiens	284-287
11009367-0	2000	Stereocontrol in rare earth metal triflate-catalyzed 1,3-dipolar cycloaddition reaction of 2-benzopyrylium-4-olate with aldehydes Exo-cycloadduct was obtained with high stereoselectivity by the addition of ytterbium triflate (Yb(OTf)(3)) (10 mol %) in the rhodium(II) acetate (Rh(2)(OAc)(4))-catalyzed decomposition of o-(methoxycarbonyl)-alpha-diazoacetophenone in the presence of benzaldehyde.	benzaldehyde	382-394	POU class 5 homeobox 1	Homo sapiens	226-235
10998257-8	2000	ALDH1 was more efficient at oxidizing acetaldehyde, propionaldehyde, and benzaldehyde and was more sensitive to disulfiram inhibition.	benzaldehyde	73-85	aldehyde dehydrogenase 1 family, member A1	Rattus norvegicus	0-5
10893244-7	2000	Furthermore, the AOH1 protein has benzaldehyde oxidizing activity with electrophoretic characteristics identical to those of a previously identified aldehyde oxidase isoenzyme (Holmes, R. S. (1979) Biochem.	benzaldehyde	34-46	aldehyde oxidase 3	Mus musculus	17-21
10956534-0	2000	Kinetic investigations of product inhibition in the amino alcohol-catalyzed asymmetric alkylation of benzaldehyde with diethylzinc In situ reaction rate measurements help to define the role of product inhibition in the asymmetric alkylation of benzaldehyde with diethylzinc using (-)-MIB as a chiral reagent.	benzaldehyde	244-256	MIB E3 ubiquitin protein ligase 1	Homo sapiens	284-287
10856427-7	2000	The two polymorphic forms of hALDH3 had identical kinetics with either benzaldehyde or aldophosphamide as substrate.	benzaldehyde	71-83	aldehyde dehydrogenase 3 family member A1	Homo sapiens	29-35
9514081-6	1998	Each inhibited NAD-linked benzaldehyde oxidation catalyzed by ALDH-3s purified from human breast adenocarcinoma MCF-7/0/CAT cells (IC50 values were 16 and 0.75 microM, respectively) and human normal stomach mucosa (IC50 values were 202 and 5 microM, respectively).	benzaldehyde	26-38	aldehyde dehydrogenase 3 family member A1	Homo sapiens	62-68
11674100-5	1999	gamma-Alkoxyallylindium reagents were prepared by treating the corresponding gamma-alkoxyallyllithium with indium trichloride and reacted with benzaldehyde to give vic-diol mono ethers in high yields with good syn selectivity.	benzaldehyde	143-155	synemin	Homo sapiens	210-213
9852085-5	1998	Purified aryl-aldehyde oxidoreductase was incubated in NMR tubes together with either carboxy-13C-benzoyl-AMP or carboxy-13C-benzoic acid to demonstrate that benzoyl-AMP is an active intermediate during the enzymatic reduction of benzoic acid to benzaldehyde.	benzaldehyde	246-258	hydroxysteroid 17-beta dehydrogenase 6	Homo sapiens	23-37
11672264-4	1998	Polymer-supported amino alcohols 5a-c have been evaluated as catalytic ligands in the enantioselective addition of diethylzinc to benzaldehyde, best results being obtained with the cis-2,6-dimethylpiperidine containing ligand 5c.	benzaldehyde	130-142	suppressor of cytokine signaling 2	Homo sapiens	181-186
10744688-7	2000	In comparison to E. coli expressing only xylMA, the presence of xylB lowered product formation rates and resulted in back formation of benzyl alcohol from benzaldehyde.	benzaldehyde	155-167	xylulokinase	Pseudomonas putida	64-68
10744688-9	2000	In the case of high fluxes through the degradation pathways and low aldehyde concentrations, XylB may contribute to benzaldehyde formation via the energetically favorable dehydrogenation of benzyl alcohols.	benzaldehyde	116-128	xylulokinase	Pseudomonas putida	93-97
10683765-3	1999	The variations were correlated to the concentrations of aldehyde oxidase activity in human subjects assayed with benzaldehyde as a substrate.	benzaldehyde	113-125	aldehyde oxidase 1	Homo sapiens	56-72
9726784-10	1998	For CYP2B1 and CYP1A1, the order of inhibitory potency was toluene > benzaldehyde > benzyl alcohol and suggests that both the parent molecule and its metabolites may act in concert to inhibit catalytic activity of these cytochromes.	benzaldehyde	72-84	cytochrome P450, family 2, subfamily b, polypeptide 1	Rattus norvegicus	4-10
9726784-10	1998	For CYP2B1 and CYP1A1, the order of inhibitory potency was toluene > benzaldehyde > benzyl alcohol and suggests that both the parent molecule and its metabolites may act in concert to inhibit catalytic activity of these cytochromes.	benzaldehyde	72-84	cytochrome P450, family 1, subfamily a, polypeptide 1	Rattus norvegicus	15-21
9161710-4	1997	Similarly, variations in aldehyde oxidase activity were found in the monkey liver preparations when assayed with benzaldehyde or N1-methylnicotinamide.	benzaldehyde	113-125	aldehyde oxidase 1	Homo sapiens	25-41
9292276-7	1997	Particularly, BA was highly toxic to the HTC cells, which possessed the highest ALDH levels.	benzaldehyde	14-16	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	80-84
9292276-8	1997	Moreover, the treatment with (diethylamino)benzaldehyde, an ALDH inhibitor, completely abolished the toxicity of BA.	benzaldehyde	113-115	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	60-64
11667478-4	1996	Among numerous solid supports of the aluminosilicate type, the K10 montmorillonite clay was found to be best at achieving quantitative formation of benzaldehyde, without any overoxidation to benzoic acid.	benzaldehyde	148-160	keratin 10	Homo sapiens	63-66
8975763-4	1996	We have found that benzaldehyde effectively inactivates the antioxidant enzyme glutathione peroxidase (Ki approximately 15 microM), but has no effect on the other antioxidant enzymes tested: catalase, superoxide dismutase, and glutathione reductase.	benzaldehyde	19-31	catalase	Rattus norvegicus	191-199
8975763-4	1996	We have found that benzaldehyde effectively inactivates the antioxidant enzyme glutathione peroxidase (Ki approximately 15 microM), but has no effect on the other antioxidant enzymes tested: catalase, superoxide dismutase, and glutathione reductase.	benzaldehyde	19-31	glutathione-disulfide reductase	Rattus norvegicus	227-248
8663198-9	1996	RalDH(II) does not recognize citral, benzaldehyde, acetaldehyde, and propanal efficiently as substrates, but does metabolize octanal and decanal efficiently.	benzaldehyde	37-49	aldehyde dehydrogenase 1 family, member A2	Rattus norvegicus	0-9
8937651-4	1996	The present investigation revealed that small amounts of this enzyme are also present in human salivary glands; mean values for ALDH-3 activities (NADP-dependent enzyme-catalysed oxidation of benzaldehyde) in cytosolic fractions prepared from submandibular and parotid glands were 52 (range: 29-92) and 44 (range: 13-73) mIU/g tissue, respectively.	benzaldehyde	192-204	aldehyde dehydrogenase 3 family member A1	Homo sapiens	128-134
7944384-2	1994	The protein radical is unstable and decays within 5 min, but the ferryl species is stable for more than 1 h. Previous studies have shown that styrene is oxidized to styrene oxide and benzaldehyde by ferric Mb and H2O2.	benzaldehyde	183-195	myoglobin	Equus caballus	206-208
8662659-10	1996	Clones expressing elevated human (386-5938 milliunits/mg) or rat (4-597 milliunits/mg, benzaldehyde/NADP+ substrate) ALDH-3 activity were 1.3- to 12-fold resistant to mafosfamide relative to control cells (<1 milliunit/mg).	benzaldehyde	87-99	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	117-123
8654195-4	1995	ALDH-3 activities (NADP-dependent catalysis of benzaldehyde oxidation) were 1.7, 212, and 183 mlU/10(7) cells in sham-electroporated MCF-7/0 cells, and MCF-7/0 cells electroporated with stomach mucosa ALDH-3 and catechol-induced MCF-7/0 ALDH-3, respectively.	benzaldehyde	47-59	aldehyde dehydrogenase 3 family member A1	Homo sapiens	0-6
8431420-6	1993	Further, the enzyme purified to homogeneity by following activity with 17-hydroxyprogesterone as a substrate was shown to reduce glucose, glyceraldehyde, and benzaldehyde (all classic aldose reductase substrates).	benzaldehyde	158-170	aldose reductase	Bos taurus	184-200
8083225-5	1994	Pretreatment of the highest activity cell line (3A1-31A) with 75 microM diethylaminobenzaldehyde, an ALDH substrate and inhibitor of benzaldehyde oxidation, effectively reversed the 3.8-fold resistance in this line; drug sensitivity was unaffected by diethylaminobenzaldehyde in the control transfected cell line.	benzaldehyde	84-96	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	101-105
8068047-4	1994	when the ability to catalyse the oxidation of aldophosphamide is normalized by the ability to catalyse the oxidation of benzaldehyde, each of these enzymes, as well as the type-2 ALDH-3 found in MCF-7/OAP cells, exhibits greater ability to catalyse the oxidation of aldophosphamide than does stomach mucosa type-1 ALDH-3; hence, although not type-2 ALDH-3s, they may be slight variants of the prototypical type-1 ALDH-3.	benzaldehyde	120-132	aldehyde dehydrogenase 3 family member A1	Homo sapiens	314-320
8068047-4	1994	when the ability to catalyse the oxidation of aldophosphamide is normalized by the ability to catalyse the oxidation of benzaldehyde, each of these enzymes, as well as the type-2 ALDH-3 found in MCF-7/OAP cells, exhibits greater ability to catalyse the oxidation of aldophosphamide than does stomach mucosa type-1 ALDH-3; hence, although not type-2 ALDH-3s, they may be slight variants of the prototypical type-1 ALDH-3.	benzaldehyde	120-132	aldehyde dehydrogenase 3 family member A1	Homo sapiens	314-320
1505055-2	1992	The induced activity could be detected with benzaldehyde as substrate and NADP as cofactor (B/NADP ALDH).	benzaldehyde	44-56	aldehyde dehydrogenase family 3, subfamily A1	Mus musculus	99-103
1483503-7	1992	BCP 54 preferentially oxidizes aromatic aldehyde such as benzaldehyde with NAD as coenzyme, but cannot oxidize phenylacetaldehyde.	benzaldehyde	31-48	aldehyde dehydrogenase 3 family member A1	Bos taurus	0-6
1483503-7	1992	BCP 54 preferentially oxidizes aromatic aldehyde such as benzaldehyde with NAD as coenzyme, but cannot oxidize phenylacetaldehyde.	benzaldehyde	57-69	aldehyde dehydrogenase 3 family member A1	Bos taurus	0-6
8168375-2	1993	(1) A genetic screen has yielded olfactory mutants, of which one, acj6, shows greatly reduced electrical responses of its olfactory organs to all odorants tested except benzaldehyde (odour of almond).	benzaldehyde	169-181	abnormal chemosensory jump 6	Drosophila melanogaster	66-70
1281448-4	1992	Measurement of the non-P450-mediated activities epoxide hydrolase, DT-diaphorase, and aldehyde dehydrogenase (NADP+, benzaldehyde) revealed < 4-fold inductions following feeding of 33 ppm Aroclor.	benzaldehyde	117-129	NAD(P)H quinone dehydrogenase 1	Rattus norvegicus	67-108
1460467-3	1992	Interestingly, abnormal chemosensory jump 6 (acj6) reduces response in the maxillary palp to all odorants tested except benzaldehyde (odor of almond), as if response to benzaldehyde is mediated through a different type of odorant pathway from the other odorants.	benzaldehyde	120-132	abnormal chemosensory jump 6	Drosophila melanogaster	45-49
1460467-3	1992	Interestingly, abnormal chemosensory jump 6 (acj6) reduces response in the maxillary palp to all odorants tested except benzaldehyde (odor of almond), as if response to benzaldehyde is mediated through a different type of odorant pathway from the other odorants.	benzaldehyde	169-181	abnormal chemosensory jump 6	Drosophila melanogaster	45-49
2060039-3	1991	The cytosolic ALDH activity of the liver was determined either with propionaldehyde and NAD (P/NAD), or with benzaldehyde and NADP (B/NADP).	benzaldehyde	109-121	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	14-18
2029738-14	1991	The inducibility of benzaldehyde:NADP aldehyde dehydrogenase in rat liver exceeds by orders of magnitude the ability of the same inducers to increase the amount of the activity of other drug metabolizing enzymes such as glutathione S-transferase, cytochrome P450 and cytochrome b5.	benzaldehyde	20-32	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	247-280
16348226-9	1990	GS-15 oxidized potential aromatic intermediates in the oxidation of toluene (benzylalcohol and benzaldehyde) and p-cresol (p-hydroxybenzylalcohol and p-hydroxybenzaldehyde).	benzaldehyde	95-107	Bet1 golgi vesicular membrane trafficking protein like	Homo sapiens	0-5
2400809-6	1990	Levels of aldehyde dehydrogenase (ALDH), which inactivates CY by prevention of formation of PhM, were significantly elevated in these CY-resistant AML cells: cytosolic and particulate ALDH fractions from these cells were 11 to 13 times control with NAD cofactor and propanal substrate and three to four times control with NADP cofactor and benzaldehyde substrate.	benzaldehyde	340-352	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	10-32
2400809-6	1990	Levels of aldehyde dehydrogenase (ALDH), which inactivates CY by prevention of formation of PhM, were significantly elevated in these CY-resistant AML cells: cytosolic and particulate ALDH fractions from these cells were 11 to 13 times control with NAD cofactor and propanal substrate and three to four times control with NADP cofactor and benzaldehyde substrate.	benzaldehyde	340-352	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	34-38
2202600-2	1990	Benzyl alcohol dehydrogenase catalyses the oxidation of benzyl alcohol to benzaldehyde with the concomitant reduction of NAD+; the reaction is reversible.	benzaldehyde	74-86	benzyl alcohol dehydrogenase	Pseudomonas putida	0-28
2202600-5	1990	The apparent Km value of benzyl alcohol dehydrogenase for benzyl alcohol was 220 microM, while that of benzaldehyde dehydrogenase for benzaldehyde was 460 microM.	benzaldehyde	103-115	benzyl alcohol dehydrogenase	Pseudomonas putida	25-53
1981531-7	1990	On the other hand, coinfusion of an electron donor for aldehyde oxidase such as 2-hydroxypyrimidine and benzaldehyde, but not xanthine, markedly stimulated the formation of DPS during hypoxia.	benzaldehyde	104-116	aldehyde oxidase 1	Homo sapiens	55-71
1981539-8	1990	These results suggest that cytochrome P-450, rather than alcohol dehydrogenase, was responsible for the metabolism of benzyl alcohol to benzaldehyde.	benzaldehyde	136-148	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	27-78
2123349-1	1990	An olfactory gene olfE, which affects response to benzaldehyde in larvae and adults of Drosophila melanogaster, has been mapped between two breakpoints on the X chromosome.	benzaldehyde	50-62	swiss cheese	Drosophila melanogaster	18-22
12692643-0	1990	NTP Toxicology and Carcinogenesis Studies of Benzaldehyde (CAS No.	benzaldehyde	45-57	BCAR1 scaffold protein, Cas family member	Rattus norvegicus	59-62
33587902-2	2021	The results show the reaction starts with the nucleophilic attack of the C2alpha atom of the HEThDP intermediate on the Cbeta atom of the carbonyl group of benzaldehyde substrate via the formation of a transition state (TS1) with the HEThDP intermediate under 4"-aminopyrimidium (APH+) form.	benzaldehyde	156-168	acylaminoacyl-peptide hydrolase	Homo sapiens	280-283
33821889-7	2021	We observed that in the presence of 5 mM H2O2, H64DOPA Mb oxidizes thioanisole and benzaldehyde with a 10 and 54 folds higher rate, respectively, as opposed to WT Mb.	benzaldehyde	83-95	myoglobin	Homo sapiens	55-57
2302256-3	1990	The fraction of cells surviving a 2 hr treatment with 10 microM cis-DDP increased from 0.012 +/- 0.004 to 0.10 +/- 0.03 when treatment was combined with at least 1 mM benzaldehyde or at least 0.2 mM salicylaldehyde.	benzaldehyde	167-179	translocase of inner mitochondrial membrane 8A	Homo sapiens	68-71
34500150-4	2022	The catalytic performance of Pd@CTF-1 was demonstrated by the one-pot N-alkylation of benzaldehyde with aniline (or nitrobenzene) under mild reaction conditions, and Pd@CTF-1 exhibited a wide range of general applicability for N-alkylation reactions.	benzaldehyde	86-98	cardiotrophin 1	Homo sapiens	32-37
34856193-3	2022	Some of these AOX substrates are odorants, such as benzaldehyde and n-octanal.	benzaldehyde	51-63	acyl-Coenzyme A oxidase 1, palmitoyl	Mus musculus	14-17
34500150-4	2022	The catalytic performance of Pd@CTF-1 was demonstrated by the one-pot N-alkylation of benzaldehyde with aniline (or nitrobenzene) under mild reaction conditions, and Pd@CTF-1 exhibited a wide range of general applicability for N-alkylation reactions.	benzaldehyde	86-98	cardiotrophin 1	Homo sapiens	169-174
34587326-5	2021	Similarly, higher levels of acrolein, benzaldehyde, crotonaldehyde, propionaldehyde, trans-2-hexenal and acetaldehyde were accumulated in aao3 mutants upon UV-C irradiation.	benzaldehyde	38-50	abscisic aldehyde oxidase 3	Arabidopsis thaliana	138-142
34302583-9	2022	PFN-1/Benzaldehyde complexes identified 20 accessible amino acids to HDX that participate in the docking simulation in the surface of WT and mutant PFN-1.	benzaldehyde	6-18	profilin 1	Homo sapiens	0-5
34302583-9	2022	PFN-1/Benzaldehyde complexes identified 20 accessible amino acids to HDX that participate in the docking simulation in the surface of WT and mutant PFN-1.	benzaldehyde	6-18	profilin 1	Homo sapiens	148-153
34893654-8	2021	Ni-Pth selectively yielded benzaldehyde.	benzaldehyde	27-39	parathyroid hormone	Homo sapiens	3-6
34587326-6	2021	Aldehydes application to plants hastened profuse senescence symptoms and higher accumulation of aldehydes, such as acrolein, benzaldehyde and 4-hydroxy-2-nonenal, in aao3 mutant leaves as compared to WT.	benzaldehyde	125-137	abscisic aldehyde oxidase 3	Arabidopsis thaliana	166-170
34689562-5	2021	When applying benzyl alcohol to consume photogenerated holes, CN/BP@Ni enables the selective production of benzaldehyde; therefore, two value-added products are obtained in a single closed redox cycle.	benzaldehyde	107-119	CCHC-type zinc finger nucleic acid binding protein	Homo sapiens	62-67
34726214-1	2021	Thiol-functionalized UiO-66-anchored atomically dispersed metal ions, denoted as UiO-66(SM)2 (M = Pd, Pt, or Au), were prepared as photocatalysts for the selective oxidation of benzyl alcohol (BA) to benzaldehyde (BAD) under visible light irradiation.	benzaldehyde	200-212	SM2	Homo sapiens	81-92
34598435-2	2021	The ligand-enabled regiocontrol, such as in the borylation of benzaldehyde, the selectivity could be switched from the ortho to meta position, under identical conditions, by just changing the external ligand (L) from 8-aminoquinoline (8-AQ) to tetramethylphenanthroline (TMP).	benzaldehyde	62-74	epithelial membrane protein 1	Homo sapiens	271-274
34138542-5	2021	Pt1/N-CNTs exhibits 99% substrate conversion with 81% yield of benzaldehyde, which is exceptional and unprecedented compared with previously reported electrocatalysts.	benzaldehyde	63-75	zinc finger protein 77	Homo sapiens	0-3
34378958-9	2021	Ald has a broad range of substrates, including benzaldehyde, furfural, and acetaldehyde.	benzaldehyde	47-59	AWN88_RS16050	Agrobacterium tumefaciens	0-3
34368547-7	2021	A maximum of 78% benzaldehyde selectivity was obtained with 0.06 g of catalyst CH1 after 18 h of toluene oxidation activity.	benzaldehyde	17-29	SUN domain containing ossification factor	Homo sapiens	79-82
34138542-6	2021	Moreover, Pt1/N-CNTs using only 0.41 wt % Pt achieved a much higher benzaldehyde yield than those of the state-of-the-art bulk Pt electrode (100 wt % Pt) and commercial Pt/C catalyst (20 wt % Pt).	benzaldehyde	68-80	zinc finger protein 77	Homo sapiens	10-13
35306285-9	2022	The developed B-mBP-ZnO catalyst exhibited superior performances in photo-oxidation of CEES to chloroethyl ethyl sulfoxide and benzyl alcohol to benzaldehyde.	benzaldehyde	145-157	growth differentiation factor 5	Mus musculus	16-19
35424977-3	2022	Moreover, the complexation behaviors of HP-beta-CD with benzaldehyde and intermediates were studied by UV-vis and 2D-ROESY NMR spectroscopies to reveal the plausible mechanisms of the reactions, and HP-beta-CD did not act as a simple phase transfer agent.	benzaldehyde	56-68	ACD shelterin complex subunit and telomerase recruitment factor	Homo sapiens	43-50
35605284-4	2022	A high H2 production rate of 8.9 mmol h-1 g-1 is delivered over the optimal ZnIn2S4/Nix-B with a stoichiometric production of benzaldehyde, which is about 22 times higher than ZnIn2S4.	benzaldehyde	126-138	BCL2 interacting protein 3 like	Homo sapiens	84-87
35452068-10	2022	Furthermore, the catalytic activity of DUT-52-(NH2)2-1" was tested in the Knoevenagel condensation between benzaldehyde and cyanoacetamide.	benzaldehyde	107-119	deoxyuridine triphosphatase	Homo sapiens	39-42
2805229-3	1989	The ALDH phenotype was determined at intervals over 42 weeks by histochemical analysis, total ALDH activity assays and gel electrophoresis using propionaldehyde and NAD (P-NAD) which characterizes class 1 and 2 ALDH, or benzaldehyde and NADP (B-NADP) to determine class 3 ALDH.	benzaldehyde	220-232	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	4-8
2755909-8	1989	An increase of the activity was also noticed when ALDH was measured with NADP and benzaldehyde (B/NADP).	benzaldehyde	82-94	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	50-54
2765201-5	1989	Alcohol-resistant AT rats had higher ALDH activity, with benzaldehyde, in most CNS structures than did the alcohol-sensitive ANT"s, significantly so in the lamina II of the somatosensory cortex and the neurons of the lateral hypothalamic area.	benzaldehyde	57-69	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	37-41
3811968-4	1986	The activity of ALDH is not only preserved, but also significantly enhanced, when propionaldehyde, phenylacetaldehyde, benzaldehyde and D-glucuronolactone are used as substrates and NAD as the coenzyme.	benzaldehyde	119-131	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	16-20
2827759-5	1987	These probes, as well as a benzaldehyde analogue of phosphatidic acid, and a water-soluble benzaldehyde reagent were covalently attached to bovine heart cytochrome c oxidase.	benzaldehyde	27-39	cytochrome c oxidase subunit 6A1, mitochondrial	Bos taurus	153-173
2827759-5	1987	These probes, as well as a benzaldehyde analogue of phosphatidic acid, and a water-soluble benzaldehyde reagent were covalently attached to bovine heart cytochrome c oxidase.	benzaldehyde	91-103	cytochrome c oxidase subunit 6A1, mitochondrial	Bos taurus	153-173
3466164-4	1986	The kcat/Km values for the reduction of benzaldehyde, 3,4-dihydroxybenzaldehyde and 4-hydroxy-3-methoxybenzaldehyde by pi ADH are from 9- to 29-fold higher than those for a class I isozyme, beta 1 gamma 2 ADH.	benzaldehyde	40-52	aldo-keto reductase family 1 member A1	Homo sapiens	122-125
3466164-4	1986	The kcat/Km values for the reduction of benzaldehyde, 3,4-dihydroxybenzaldehyde and 4-hydroxy-3-methoxybenzaldehyde by pi ADH are from 9- to 29-fold higher than those for a class I isozyme, beta 1 gamma 2 ADH.	benzaldehyde	40-52	aldo-keto reductase family 1 member A1	Homo sapiens	205-208
3343508-9	1988	AlDH in upper GI tissues and in liver nodules shared three characteristics: a sharp localization; a preference for Bz and NADP compared to the aliphatic substrate acetaldehyde and NAD; and a high co-enzyme-independent activity in the presence of Bz.	benzaldehyde	115-117	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	0-4
3343508-9	1988	AlDH in upper GI tissues and in liver nodules shared three characteristics: a sharp localization; a preference for Bz and NADP compared to the aliphatic substrate acetaldehyde and NAD; and a high co-enzyme-independent activity in the presence of Bz.	benzaldehyde	246-248	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	0-4
3811968-5	1986	A relative increase of activity is also noted when ALDH is measured with benzaldehyde and NADP.	benzaldehyde	73-85	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	51-55
3003181-1	1986	Hepatocarcinogenesis in rats treated with several chemicals is associated with changes in aldehyde dehydrogenase (AlDH) activity, particularly heterogeneous expression of a "tumor specific" phenotype that is very active with aromatic aldehydes, e.g., benzaldehyde (Bz).	benzaldehyde	251-263	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	90-112
3008991-2	1986	Like the tumor-associated aldehyde dehydrogenase, bladder NADP+-ALDH is cytosolic and preferentially oxidizes benzaldehyde-like aromatic aldehydes.	benzaldehyde	110-122	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	26-48
3008991-2	1986	Like the tumor-associated aldehyde dehydrogenase, bladder NADP+-ALDH is cytosolic and preferentially oxidizes benzaldehyde-like aromatic aldehydes.	benzaldehyde	110-122	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	64-68
3083781-3	1986	In an NADPH-supported reduction reaction, aldose reductase exhibited similar activity toward benzaldehyde and glyceraldehyde, but benzyl alcohol was a much better substrate than physiological polyols in the analog-dependent oxidation reaction: relative kcat/Km ratios were 740 for benzyl alcohol, 2.2 for xylitol, and 1.0 for glycerol.	benzaldehyde	93-105	aldo-keto reductase family 1 member B1	Rattus norvegicus	42-58
3003181-2	1986	Objectives of this study were first, to determine if liver cancers in vinyl chloride-treated rats also expressed this AlDH phenotype, and second, to quantitate the NAD- and NADP-dependent AlDH activity for the substrates Bz and acetaldehyde (Ac) in the cancers and surrounding tissue.	benzaldehyde	221-223	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	118-122
3003181-2	1986	Objectives of this study were first, to determine if liver cancers in vinyl chloride-treated rats also expressed this AlDH phenotype, and second, to quantitate the NAD- and NADP-dependent AlDH activity for the substrates Bz and acetaldehyde (Ac) in the cancers and surrounding tissue.	benzaldehyde	221-223	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	188-192
3003181-1	1986	Hepatocarcinogenesis in rats treated with several chemicals is associated with changes in aldehyde dehydrogenase (AlDH) activity, particularly heterogeneous expression of a "tumor specific" phenotype that is very active with aromatic aldehydes, e.g., benzaldehyde (Bz).	benzaldehyde	251-263	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	114-118
3003181-1	1986	Hepatocarcinogenesis in rats treated with several chemicals is associated with changes in aldehyde dehydrogenase (AlDH) activity, particularly heterogeneous expression of a "tumor specific" phenotype that is very active with aromatic aldehydes, e.g., benzaldehyde (Bz).	benzaldehyde	265-267	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	90-112
3003181-1	1986	Hepatocarcinogenesis in rats treated with several chemicals is associated with changes in aldehyde dehydrogenase (AlDH) activity, particularly heterogeneous expression of a "tumor specific" phenotype that is very active with aromatic aldehydes, e.g., benzaldehyde (Bz).	benzaldehyde	265-267	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	114-118
3994763-4	1985	When the Km values for benzaldehyde with aldehyde dehydrogenase (ALDH) were determined, two Km values (3 and 120 microM) were obtained with mitochondria, but only a single Km value (25 microM) was obtained with the cytosolic fraction.	benzaldehyde	23-35	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	41-63
4073832-3	1985	The ALDH3 isozymes show optimal activity with benzaldehyde and can use either NAD or NADP as cofactor.	benzaldehyde	46-58	aldehyde dehydrogenase 3 family member A1	Homo sapiens	4-9
3994763-4	1985	When the Km values for benzaldehyde with aldehyde dehydrogenase (ALDH) were determined, two Km values (3 and 120 microM) were obtained with mitochondria, but only a single Km value (25 microM) was obtained with the cytosolic fraction.	benzaldehyde	23-35	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	65-69
3994763-6	1985	In intact mitochondria, with 200 microM acetaldehyde or benzaldehyde the matrix space enzyme accounted for 77 and 62%, respectively, of the total ALDH activity.	benzaldehyde	56-68	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	146-150
3994763-13	1985	It can be concluded that, in rat, disulfiram inhibiting liver ALDH not only affects oxidation of acetaldehyde, but also that of benzaldehyde.	benzaldehyde	128-140	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	62-66
4015840-3	1985	One isozyme, designated ALDH3, which is very active against benzaldehyde, was found to show variable expression in hybrids made between rat hepatoma cells and human fibroblasts or fetal liver.	benzaldehyde	60-72	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	24-29
6149820-2	1984	The hepatic ALDH phenotype was determined at intervals over 280 days by histochemical analysis, total ALDH activity assays and gel electrophoresis, using propionaldehyde and NAD (P/NAD) to characterize normal liver ALDH activity or benzaldehyde and NADP (B/NADP) to determine tumor-associated ALDH activity.	benzaldehyde	232-244	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	12-16
4226961-3	1967	When the aromatic aldehyde benzaldehyde is used as substrate, human liver aldehyde oxidase, like the rabbit enzyme, is strongly inhibited by menadione, estradiol-17beta, antimycin A, Triton X-100, and N-alkylphenothiazines; the human enzyme differs from the rabbit enzyme, however, in being relatively insensitive to oligomycin and Amytal.	benzaldehyde	27-39	aldehyde oxidase 1	Homo sapiens	74-90
6662893-3	1983	p-Sulfamoylbenzaldehyde and benzaldehyde formed enzymatically from p-sulfamoylbenzylamine (the substrate of monoamine oxidase A) and benzylamine (the substrate of monoamine oxidase B), respectively, are converted simultaneously into fluorescent compounds with 2,2"-dithiobis(1-aminonaphthalene).	benzaldehyde	11-23	monoamine oxidase A	Rattus norvegicus	108-127
6662893-3	1983	p-Sulfamoylbenzaldehyde and benzaldehyde formed enzymatically from p-sulfamoylbenzylamine (the substrate of monoamine oxidase A) and benzylamine (the substrate of monoamine oxidase B), respectively, are converted simultaneously into fluorescent compounds with 2,2"-dithiobis(1-aminonaphthalene).	benzaldehyde	11-23	monoamine oxidase B	Rattus norvegicus	163-182
6196110-5	1983	During hepatocarcinogenesis, ALDH staining patterns in grossly normal liver range from normal-appearing to patterns of distinct, intense focal hepatocyte staining with propionaldehyde-NAD and/or benzaldehyde-NADP.	benzaldehyde	195-207	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	29-33
6196110-8	1983	Neoplasms with elevated ALDH activity with propionaldehyde-NAD and/or benzaldehyde-NADP, as well as with no detectable ALDH, have been observed.	benzaldehyde	70-82	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	24-28
27359-9	1978	Transient-state rate parameters for benzyl alcohol/benzaldehyde catalysis by liver alcohol dehydrogenase have been determined at different pH.	benzaldehyde	51-63	aldo-keto reductase family 1 member A1	Homo sapiens	83-104
235278-9	1975	The equilibrium constant for hydride transfer from benzaldehyde to benzyl alcohol at pH 8.75 is K-eq equals kappa-H/kappa-H equals 42; this constant has important consequences concerning subunit interactions during liver alcohol dehydrogenase catalysis.	benzaldehyde	51-63	aldo-keto reductase family 1 member A1	Homo sapiens	221-242
6488182-4	1984	HTC, JM1, and JM2 express the tumor ALDH phenotype, as indicated by elevated NADP-dependent, benzaldehyde-oxidizing activity, the appearance of new isozymes by electrophoresis, and characteristic histochemical localization of ALDH activity in situ.	benzaldehyde	93-105	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	36-40
6388629-1	1984	The reduction of benzaldehyde and p-nitrobenzaldehyde by NADH, catalyzed by horse liver alcohol dehydrogenase (LADH), has been found to be faster when NADH is bound to glyceraldehyde-3-phosphate dehydrogenase (GPDH) than with free NADH.	benzaldehyde	17-29	glyceraldehyde-3-phosphate dehydrogenase	Equus caballus	168-208
6388629-1	1984	The reduction of benzaldehyde and p-nitrobenzaldehyde by NADH, catalyzed by horse liver alcohol dehydrogenase (LADH), has been found to be faster when NADH is bound to glyceraldehyde-3-phosphate dehydrogenase (GPDH) than with free NADH.	benzaldehyde	17-29	glyceraldehyde-3-phosphate dehydrogenase	Equus caballus	210-214
33141452-4	2021	In the presence of phenylcarbinol, ACN exhibited excellent pure water-splitting ability (95.3 mumol/h) and in the meanwhile phenylcarbinol was selectively oxidized to benzaldehyde (conversion of 90.9%, selectivity of 99.7%) under solar irradiation.	benzaldehyde	167-179	NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor	Homo sapiens	35-38
34039986-6	2021	The produced Pt2/mpg-C3N4 samples are versatile and can be applied in catalyzing other important reactions, such as the selective hydrogenation of benzaldehyde and the epoxidation of styrene.	benzaldehyde	147-159	N-methylpurine DNA glycosylase	Homo sapiens	17-20
33617080-4	2021	Deprotonation of Si(C2F5)3H with sterically demanding phosphazene bases afforded thermally stable phosphazenium salts of the [Si(C2F5)3]- anion, which add to benzaldehyde, benzophenone, CS2 and CO2in various manners.	benzaldehyde	158-170	chorionic somatomammotropin hormone 2	Homo sapiens	186-189
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).	benzaldehyde	214-226	arylformamidase	Homo sapiens	264-266
33832752-2	2021	The results show the reaction starts with the nucleophilic attack of the C2alpha atom of the HEThDP intermediate on the Cbeta atom of the carbonyl group of benzaldehyde substrate via the formation of a transition state (TS1) with the HEThDP intermediate under 4"-aminopyrimidium (APH+) form.	benzaldehyde	156-168	acylaminoacyl-peptide hydrolase	Homo sapiens	280-283
33454360-3	2021	Data from read-across analog benzaldehyde (CAS # 100-52-7) show that p-tolualdehyde is not expected to be genotoxic.	benzaldehyde	29-41	BCAR1 scaffold protein, Cas family member	Homo sapiens	43-46
33563272-5	2021	Benzaldehyde preconditioning activates systemic cytoprotective stress responses involving DAF-16/FOXO, SKN-1/Nrf2, and Hsp90 in non-neuronal cells, which confer both physiological (increased survival) and behavioral tolerance (reduced food avoidance) to benzaldehyde exposure.	benzaldehyde	0-12	NFE2 like bZIP transcription factor 2	Homo sapiens	109-113
33563272-5	2021	Benzaldehyde preconditioning activates systemic cytoprotective stress responses involving DAF-16/FOXO, SKN-1/Nrf2, and Hsp90 in non-neuronal cells, which confer both physiological (increased survival) and behavioral tolerance (reduced food avoidance) to benzaldehyde exposure.	benzaldehyde	0-12	heat shock protein 90 alpha family class A member 1	Homo sapiens	119-124
33397797-0	2021	The G-protein coupled receptor SRX-97 is required for concentration dependent sensing of benzaldehyde in Caenorhabditis elegans.	benzaldehyde	89-101	7TM_GPCR_Srx domain-containing protein	Caenorhabditis elegans	31-37
33397797-7	2021	Analysis of CRISPR-based deletion mutants of the srx-97 locus suggests that this gene is involved in recognition of high concentrations of benzaldehyde.	benzaldehyde	139-151	7TM_GPCR_Srx domain-containing protein	Caenorhabditis elegans	49-55