BindingDB PrimarySearch

Found 49 hits of affinity data for UniProtKB/TrEMBL: P80404
Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	k_off s^-1	k_on M^-1s^-1	pH	Temp °C
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50024968 ((2Z)-4-ammonio-2-(fluoromethyl)but-2-enoate \| CHEM...) Show SMILES [NH3+]C\C=C(/CF)C([O-])=O Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	9.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for the inhibitory effect against Gamma-amino-N-butyrate transaminase from bacteria				J Med Chem 29: 764-70 (1986) BindingDB Entry DOI: 10.7270/Q2668C6T
TBA Curated by ChEMBL					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50021645 ((3-Phenyl-thioureido)-acetic acid \| CHEMBL311337 \|...) Show SMILES OC(=O)CNC(=S)Nc1ccccc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem	PubMed	9.10E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for inhibition of Gamma-amino-N-butyrate transaminase				J Med Chem 30: 239-49 (1987) BindingDB Entry DOI: 10.7270/Q2SF2V5K
TBA Curated by ChEMBL					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50118885 (5-Amino-cyclohex-3-enecarboxylic acid \| CHEMBL1379...) Show SMILES N[C@@H]1C[C@H](CC=C1)C(O)=O \|c:5\| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University Curated by ChEMBL					Assay Description Binding affinity against Gamma-amino-N-butyrate transaminase				J Med Chem 45: 4531-9 (2002) BindingDB Entry DOI: 10.7270/Q2G1605T
Northwestern University Curated by ChEMBL					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50118884 (2-Amino-cyclohex-3-enecarboxylic acid \| CHEMBL1419...) Show SMILES N[C@H]1C=CCC[C@@H]1C(O)=O \|c:2\| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	1.25E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University Curated by ChEMBL					Assay Description Binding affinity against Gamma-amino-N-butyrate transaminase				J Med Chem 45: 4531-9 (2002) BindingDB Entry DOI: 10.7270/Q2G1605T
Northwestern University Curated by ChEMBL					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM323799 ((2S,4S)-4-Aminotetrahydrothiophene-2-carboxylic ac...) Show SMILES N[C@@H]1CS[C@@H](C1)C(O)=O Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	US Patent	1.82E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University US Patent					Assay Description Biochemical assays were performed using a Biotek Synergy H1 microplate reader. Prior to their evaluation, initial experiments were performed to confi...				US Patent US10189807 (2019) BindingDB Entry DOI: 10.7270/Q2C82CDG
Northwestern University US Patent					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM466532 (US10800753, Compound 17) Show SMILES COC(=O)[C@@H]1C[C@H](N)CS1 \|r\| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	US Patent	1.82E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University US Patent					Assay Description Inhibition constants were determined by monitoring GABA-AT activity in the presence of 0-50 mM concentrations of synthesized analogues using a couple...				US Patent US10800753 (2020) BindingDB Entry DOI: 10.7270/Q2ZC85ZR
Northwestern University US Patent					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50118886 (4-Amino-hex-5-enoic acid \| CHEMBL89598 \| US1018980...) Show SMILES NC(CCC(O)=O)C=C Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid UniChem Patents Similars	DrugBank PubMed	8.50E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University Curated by ChEMBL					Assay Description Concentration dependent inactivation of Gamma-amino-N-butyrate transaminase				J Med Chem 45: 4531-9 (2002) BindingDB Entry DOI: 10.7270/Q2G1605T
Northwestern University Curated by ChEMBL					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM323800 ((2R,4S)-4-Aminotetrahydrothiophene-2-carboxylic ac...) Show SMILES N[C@@H]1CS[C@H](C1)C(O)=O Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	2.23E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University US Patent					Assay Description Inhibition constants were determined by monitoring GABA-AT activity in the presence of 0-50 mM concentrations of synthesized analogues using a couple...				US Patent US10800753 (2020) BindingDB Entry DOI: 10.7270/Q2ZC85ZR
Northwestern University US Patent					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM323800 ((2R,4S)-4-Aminotetrahydrothiophene-2-carboxylic ac...) Show SMILES N[C@@H]1CS[C@H](C1)C(O)=O Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	2.23E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University US Patent					Assay Description Biochemical assays were performed using a Biotek Synergy H1 microplate reader. Prior to their evaluation, initial experiments were performed to confi...				US Patent US10189807 (2019) BindingDB Entry DOI: 10.7270/Q2C82CDG
Northwestern University US Patent					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50118888 (5-Amino-cyclohex-3-enecarboxylic acid \| CHEMBL3368...) Show SMILES N[C@H]1C[C@H](CC=C1)C(O)=O \|c:5\| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	2.30E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University Curated by ChEMBL					Assay Description Concentration dependent inactivation of gGamma-amino-N-butyrate transaminase				J Med Chem 45: 4531-9 (2002) BindingDB Entry DOI: 10.7270/Q2G1605T
Northwestern University Curated by ChEMBL					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM323801 ((4S)-4-Aminotetrahydrothiophene-2-carboxylic acid ...) Show SMILES Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	US Patent	3.20E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University US Patent					Assay Description Biochemical assays were performed using a Biotek Synergy H1 microplate reader. Prior to their evaluation, initial experiments were performed to confi...				US Patent US10189807 (2019) BindingDB Entry DOI: 10.7270/Q2C82CDG
Northwestern University US Patent					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50357219 (CHEMBL1361446 \| US10800753, Compound (S)-vigabatri...) Show SMILES N[C@H](CCC(O)=O)C=C Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Similars	US Patent	3.20E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University US Patent					Assay Description Inhibition constants were determined by monitoring GABA-AT activity in the presence of 0-50 mM concentrations of synthesized analogues using a couple...				US Patent US10800753 (2020) BindingDB Entry DOI: 10.7270/Q2ZC85ZR
Northwestern University US Patent					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50118886 (4-Amino-hex-5-enoic acid \| CHEMBL89598 \| US1018980...) Show SMILES NC(CCC(O)=O)C=C Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid UniChem Patents Similars	DrugBank Article PubMed	3.20E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University Curated by ChEMBL					Assay Description Inactivation of GABA-AT				J Med Chem 55: 357-66 (2012) Article DOI: 10.1021/jm201231w BindingDB Entry DOI: 10.7270/Q2QF8V1F
Northwestern University Curated by ChEMBL					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50118886 (4-Amino-hex-5-enoic acid \| CHEMBL89598 \| US1018980...) Show SMILES NC(CCC(O)=O)C=C Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid UniChem Patents Similars	DrugBank US Patent	3.20E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University US Patent					Assay Description Biochemical assays were performed using a Biotek Synergy H1 microplate reader. Prior to their evaluation, initial experiments were performed to confi...				US Patent US10189807 (2019) BindingDB Entry DOI: 10.7270/Q2C82CDG
Northwestern University US Patent					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM466536 (US10800753, Compound 19) Show SMILES N[C@H]1CC(C(O)=O)S(=O)(=O)C1 \|r\| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	US Patent	3.20E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University US Patent					Assay Description Inhibition constants were determined by monitoring GABA-AT activity in the presence of 0-50 mM concentrations of synthesized analogues using a couple...				US Patent US10800753 (2020) BindingDB Entry DOI: 10.7270/Q2ZC85ZR
Northwestern University US Patent					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM466538 (US10800753, Compound 21) Show SMILES N[C@H]1CS[C@@H](C1)C(O)=O \|r\| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	3.30E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University US Patent					Assay Description Inhibition constants were determined by monitoring GABA-AT activity in the presence of 0-50 mM concentrations of synthesized analogues using a couple...				US Patent US10800753 (2020) BindingDB Entry DOI: 10.7270/Q2ZC85ZR
Northwestern University US Patent					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM323803 (US10189807, Compound 21) Show SMILES [NH3+][C@H]1CS[C@@H](C1)C([O-])=O Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	3.30E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University US Patent					Assay Description Biochemical assays were performed using a Biotek Synergy H1 microplate reader. Prior to their evaluation, initial experiments were performed to confi...				US Patent US10189807 (2019) BindingDB Entry DOI: 10.7270/Q2C82CDG
Northwestern University US Patent					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM466537 (US10800753, Compound 20) Show SMILES N[C@H]1CS[C@H](C1)C(O)=O \|r\| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	3.40E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University US Patent					Assay Description Inhibition constants were determined by monitoring GABA-AT activity in the presence of 0-50 mM concentrations of synthesized analogues using a couple...				US Patent US10800753 (2020) BindingDB Entry DOI: 10.7270/Q2ZC85ZR
Northwestern University US Patent					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM323802 (US10189807, Compound 20) Show SMILES [NH3+][C@H]1CS[C@H](C1)C([O-])=O Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	3.40E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University US Patent					Assay Description Biochemical assays were performed using a Biotek Synergy H1 microplate reader. Prior to their evaluation, initial experiments were performed to confi...				US Patent US10189807 (2019) BindingDB Entry DOI: 10.7270/Q2C82CDG
Northwestern University US Patent					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50082127 (3-(ammoniomethyl)-2,6-difluorobenzenolate \| 3-Amin...) Show SMILES [NH3+]Cc1ccc(F)c([O-])c1F Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	6.30E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Competitive inhibition of GABA aminotransferase (unknown origin)				J Med Chem 61: 5822-5880 (2018) Article DOI: 10.1021/acs.jmedchem.7b01788 BindingDB Entry DOI: 10.7270/Q232008T
Bristol-Myers Squibb Curated by ChEMBL					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50082127 (3-(ammoniomethyl)-2,6-difluorobenzenolate \| 3-Amin...) Show SMILES [NH3+]Cc1ccc(F)c([O-])c1F Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	6.30E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Competitive inhibition of GABA aminotransferase				J Med Chem 54: 2529-91 (2011) Article DOI: 10.1021/jm1013693 BindingDB Entry DOI: 10.7270/Q24M95PH
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM466539 (US10800753, Compound 22) Show SMILES N[C@@H]1CC(C(O)=O)S(=O)(=O)C1 \|r\| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	US Patent	7.50E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University US Patent					Assay Description Inhibition constants were determined by monitoring GABA-AT activity in the presence of 0-50 mM concentrations of synthesized analogues using a couple...				US Patent US10800753 (2020) BindingDB Entry DOI: 10.7270/Q2ZC85ZR
Northwestern University US Patent					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM323805 (US10189807, Compound 22) Show SMILES [NH3+][C@@H]1CC(C([O-])=O)S(=O)(=O)C1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	US Patent	7.50E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University US Patent					Assay Description Biochemical assays were performed using a Biotek Synergy H1 microplate reader. Prior to their evaluation, initial experiments were performed to confi...				US Patent US10189807 (2019) BindingDB Entry DOI: 10.7270/Q2C82CDG
Northwestern University US Patent					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50073151 (4-(ammoniomethyl)-2,6-difluorobenzenolate \| 4-Amin...) Show SMILES NCc1cc(F)c(O)c(F)c1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.10E+7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Competitive inhibition of GABA aminotransferase				J Med Chem 54: 2529-91 (2011) Article DOI: 10.1021/jm1013693 BindingDB Entry DOI: 10.7270/Q24M95PH
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50073151 (4-(ammoniomethyl)-2,6-difluorobenzenolate \| 4-Amin...) Show SMILES NCc1cc(F)c(O)c(F)c1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.10E+7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Competitive inhibition of GABA aminotransferase (unknown origin)				J Med Chem 61: 5822-5880 (2018) Article DOI: 10.1021/acs.jmedchem.7b01788 BindingDB Entry DOI: 10.7270/Q232008T
Bristol-Myers Squibb Curated by ChEMBL					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50118887 (2-Amino-cyclohex-3-enecarboxylic acid \| CHEMBL1384...) Show SMILES N[C@@H]1C=CCC[C@@H]1C(O)=O \|c:2\| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	1.30E+7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University Curated by ChEMBL					Assay Description Concentration dependent inactivation of Gamma-amino-N-butyrate transaminase				J Med Chem 45: 4531-9 (2002) BindingDB Entry DOI: 10.7270/Q2G1605T
Northwestern University Curated by ChEMBL					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50177407 (1-(4-hydroxyphenyl)prop-2-en-1-one \| 4-acryloylphe...) Show SMILES Oc1ccc(cc1)C(=O)C=C Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	5.48E+3	n/a	n/a	n/a	n/a	n/a	n/a
Huazhong University of Science and Technology Curated by ChEMBL					Assay Description Inhibitory activity against GABAT				Bioorg Med Chem Lett 16: 592-5 (2005) Article DOI: 10.1016/j.bmcl.2005.10.040 BindingDB Entry DOI: 10.7270/Q29G5MCH
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50177412 (4-(aminomethyl)phenol \| 4-hydroxybenzylamine \| CHE...) Show SMILES NCc1ccc(O)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.54E+4	n/a	n/a	n/a	n/a	n/a	n/a
Huazhong University of Science and Technology Curated by ChEMBL					Assay Description Inhibitory activity against GABAT				Bioorg Med Chem Lett 16: 592-5 (2005) Article DOI: 10.1016/j.bmcl.2005.10.040 BindingDB Entry DOI: 10.7270/Q29G5MCH
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50177410 (4-hydroxy-3-nitrobenzaldehyde \| CHEMBL378361) Show SMILES Oc1ccc(C=O)cc1[N+]([O-])=O Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.55E+4	n/a	n/a	n/a	n/a	n/a	n/a
Huazhong University of Science and Technology Curated by ChEMBL					Assay Description Inhibitory activity against GABAT				Bioorg Med Chem Lett 16: 592-5 (2005) Article DOI: 10.1016/j.bmcl.2005.10.040 BindingDB Entry DOI: 10.7270/Q29G5MCH
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50177411 (4-formylphenol \| 4-hydroxybenzaldehyde \| CHEMBL141...) Show SMILES Oc1ccc(C=O)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.65E+4	n/a	n/a	n/a	n/a	n/a	n/a
Huazhong University of Science and Technology Curated by ChEMBL					Assay Description Inhibitory activity against GABAT				Bioorg Med Chem Lett 16: 592-5 (2005) Article DOI: 10.1016/j.bmcl.2005.10.040 BindingDB Entry DOI: 10.7270/Q29G5MCH
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50177405 (3-methoxy-4-hydroxybenzaldehyde \| 4-hydroxy-3-meth...) Show SMILES COc1cc(C=O)ccc1O Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.71E+4	n/a	n/a	n/a	n/a	n/a	n/a
Huazhong University of Science and Technology Curated by ChEMBL					Assay Description Inhibitory activity against GABAT				Bioorg Med Chem Lett 16: 592-5 (2005) Article DOI: 10.1016/j.bmcl.2005.10.040 BindingDB Entry DOI: 10.7270/Q29G5MCH
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50177402 (1-(4-hydroxy-phenyl)-propan-1-one \| 1-(4-hydroxyph...) Show SMILES CCC(=O)c1ccc(O)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.76E+5	n/a	n/a	n/a	n/a	n/a	n/a
Huazhong University of Science and Technology Curated by ChEMBL					Assay Description Inhibitory activity against GABAT				Bioorg Med Chem Lett 16: 592-5 (2005) Article DOI: 10.1016/j.bmcl.2005.10.040 BindingDB Entry DOI: 10.7270/Q29G5MCH
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50177409 ((4-hydroxyphenyl)ethan-1-one \| 1-(4-hydroxyphenyl)...) Show SMILES CC(=O)c1ccc(O)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.88E+5	n/a	n/a	n/a	n/a	n/a	n/a
Huazhong University of Science and Technology Curated by ChEMBL					Assay Description Inhibitory activity against GABAT				Bioorg Med Chem Lett 16: 592-5 (2005) Article DOI: 10.1016/j.bmcl.2005.10.040 BindingDB Entry DOI: 10.7270/Q29G5MCH
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50177404 (4-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymet...) Show SMILES Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Huazhong University of Science and Technology Curated by ChEMBL					Assay Description Inhibitory activity against GABAT				Bioorg Med Chem Lett 16: 592-5 (2005) Article DOI: 10.1016/j.bmcl.2005.10.040 BindingDB Entry DOI: 10.7270/Q29G5MCH
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50145829 (4-Aminobenzoesaeure \| 4-aminobenzoic acid \| CHEMBL...) Show SMILES Nc1ccc(cc1)C(O)=O Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Huazhong University of Science and Technology Curated by ChEMBL					Assay Description Inhibitory activity against GABAT				Bioorg Med Chem Lett 16: 592-5 (2005) Article DOI: 10.1016/j.bmcl.2005.10.040 BindingDB Entry DOI: 10.7270/Q29G5MCH
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50177403 ((2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(4-(hydroxyme...) Show SMILES Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Huazhong University of Science and Technology Curated by ChEMBL					Assay Description Inhibitory activity against GABAT				Bioorg Med Chem Lett 16: 592-5 (2005) Article DOI: 10.1016/j.bmcl.2005.10.040 BindingDB Entry DOI: 10.7270/Q29G5MCH
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50177406 (4-hydroxybenzaldehyde oxime \| CHEMBL202611) Show SMILES Oc1ccc(CN=O)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Huazhong University of Science and Technology Curated by ChEMBL					Assay Description Inhibitory activity against GABAT				Bioorg Med Chem Lett 16: 592-5 (2005) Article DOI: 10.1016/j.bmcl.2005.10.040 BindingDB Entry DOI: 10.7270/Q29G5MCH
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50177408 (4-(hydroxymethyl)phenol \| 4-Hydroxybenzyl alcohol ...) Show SMILES OCc1ccc(O)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Huazhong University of Science and Technology Curated by ChEMBL					Assay Description Inhibitory activity against GABAT				Bioorg Med Chem Lett 16: 592-5 (2005) Article DOI: 10.1016/j.bmcl.2005.10.040 BindingDB Entry DOI: 10.7270/Q29G5MCH
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50139370 (4-Methoxy-benzaldehyde \| 4-methoxybenzaldehyde \| C...) Show SMILES COc1ccc(C=O)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Huazhong University of Science and Technology Curated by ChEMBL					Assay Description Inhibitory activity against GABAT				Bioorg Med Chem Lett 16: 592-5 (2005) Article DOI: 10.1016/j.bmcl.2005.10.040 BindingDB Entry DOI: 10.7270/Q29G5MCH
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50177413 (4-hydroxy-3-methoxybenzaldehyde oxime \| CHEMBL2024...) Show SMILES COc1cc(CN=O)ccc1O Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Huazhong University of Science and Technology Curated by ChEMBL					Assay Description Inhibitory activity against GABAT				Bioorg Med Chem Lett 16: 592-5 (2005) Article DOI: 10.1016/j.bmcl.2005.10.040 BindingDB Entry DOI: 10.7270/Q29G5MCH
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM26194 (4-Hydroxybenzoate, III \| 4-hydroxybenzoic acid \| C...) Show SMILES OC(=O)c1ccc(O)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Huazhong University of Science and Technology Curated by ChEMBL					Assay Description Inhibitory activity against GABAT				Bioorg Med Chem Lett 16: 592-5 (2005) Article DOI: 10.1016/j.bmcl.2005.10.040 BindingDB Entry DOI: 10.7270/Q29G5MCH
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50376752 (CHEMBL535644) Show SMILES NCc1ccccc1CC(O)=O Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem	Article PubMed	n/a	n/a	>5.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University Curated by ChEMBL					Assay Description Inhibition of GABA-AT				Bioorg Med Chem Lett 18: 3122-5 (2008) Article DOI: 10.1016/j.bmcl.2007.10.060 BindingDB Entry DOI: 10.7270/Q22J6CRF
Northwestern University Curated by ChEMBL					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50376753 (CHEMBL535415) Show SMILES NCc1ccccc1C(O)=O Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem	Article PubMed	n/a	n/a	>5.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University Curated by ChEMBL					Assay Description Inhibition of GABA-AT				Bioorg Med Chem Lett 18: 3122-5 (2008) Article DOI: 10.1016/j.bmcl.2007.10.060 BindingDB Entry DOI: 10.7270/Q22J6CRF
Northwestern University Curated by ChEMBL					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50376754 (CHEMBL535865) Show SMILES Nc1cccc(CC(O)=O)c1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem	Article PubMed	n/a	n/a	>5.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University Curated by ChEMBL					Assay Description Inhibition of GABA-AT				Bioorg Med Chem Lett 18: 3122-5 (2008) Article DOI: 10.1016/j.bmcl.2007.10.060 BindingDB Entry DOI: 10.7270/Q22J6CRF
Northwestern University Curated by ChEMBL					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50376750 (CHEMBL541141) Show SMILES NCc1cccc(c1)C(O)=O Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem	Article PubMed	n/a	n/a	>5.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University Curated by ChEMBL					Assay Description Inhibition of GABA-AT				Bioorg Med Chem Lett 18: 3122-5 (2008) Article DOI: 10.1016/j.bmcl.2007.10.060 BindingDB Entry DOI: 10.7270/Q22J6CRF
Northwestern University Curated by ChEMBL					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50226518 (3-Aminobenzoesaeure \| 3-aminobenzoic acid \| CHEMBL...) Show SMILES Nc1cccc(c1)C(O)=O Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	>5.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University Curated by ChEMBL					Assay Description Inhibition of GABA-AT				Bioorg Med Chem Lett 18: 3122-5 (2008) Article DOI: 10.1016/j.bmcl.2007.10.060 BindingDB Entry DOI: 10.7270/Q22J6CRF
Northwestern University Curated by ChEMBL					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50376751 (ANTHRANILIC ACID) Show SMILES Nc1ccccc1C(O)=O Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase DrugBank KEGG MMDB PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University Curated by ChEMBL					Assay Description Inhibition of GABA-AT				Bioorg Med Chem Lett 18: 3122-5 (2008) Article DOI: 10.1016/j.bmcl.2007.10.060 BindingDB Entry DOI: 10.7270/Q22J6CRF
Northwestern University Curated by ChEMBL					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50376755 (CHEMBL535643) Show SMILES NCc1cccc(CC(O)=O)c1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid PDB UniChem	Article PubMed	n/a	n/a	>5.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Northwestern University Curated by ChEMBL					Assay Description Inhibition of GABA-AT				Bioorg Med Chem Lett 18: 3122-5 (2008) Article DOI: 10.1016/j.bmcl.2007.10.060 BindingDB Entry DOI: 10.7270/Q22J6CRF
Northwestern University Curated by ChEMBL					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM50009001 (5,6,7-Trihydroxyflavone \| 5,6,7-trihydroxy-2-pheny...) Show SMILES Oc1cc2oc(cc(=O)c2c(O)c1O)-c1ccccc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.28E+7	n/a	n/a	n/a	n/a	n/a	n/a
Punjabi University Curated by ChEMBL					Assay Description Inhibition of GABA transaminase (unknown origin)				Eur J Med Chem 84: 206-39 (2014) Article DOI: 10.1016/j.ejmech.2014.07.013 BindingDB Entry DOI: 10.7270/Q2GH9KMN
Punjabi University Curated by ChEMBL					More data for this Ligand-Target Pair