Compile Data Set for Download or QSAR

Found 26 hits of ki data for polymerid = 50000150   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon 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 InChI=1S/C5H8FNO2/c6-3-4(1-2-7)5(8)9/h1H,2-3,7H2,(H,8,9)/b4-1+	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
					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 InChI=1S/C9H10N2O2S/c12-8(13)6-10-9(14)11-7-4-2-1-3-5-7/h1-5H,6H2,(H,12,13)(H2,10,11,14)	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
					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 InChI=1S/C7H11NO2/c8-6-3-1-2-5(4-6)7(9)10/h1,3,5-6H,2,4,8H2,(H,9,10)/t5-,6-/m0/s1	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
					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 InChI=1S/C7H11NO2/c8-6-4-2-1-3-5(6)7(9)10/h2,4-6H,1,3,8H2,(H,9,10)/t5-,6-/m0/s1	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
					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 InChI=1S/C5H9NO2S/c6-3-1-4(5(7)8)9-2-3/h3-4H,1-2,6H2,(H,7,8)/t3-,4-/m0/s1	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
					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 InChI=1S/C6H11NO2S/c1-9-6(8)5-2-4(7)3-10-5/h4-5H,2-3,7H2,1H3/t4-,5-/m0/s1	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
					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 InChI=1S/C6H11NO2/c1-2-5(7)3-4-6(8)9/h2,5H,1,3-4,7H2,(H,8,9)	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
					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 InChI=1S/C5H9NO2S/c6-3-1-4(5(7)8)9-2-3/h3-4H,1-2,6H2,(H,7,8)/t3-,4+/m0/s1	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
					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 InChI=1S/C5H9NO2S/c6-3-1-4(5(7)8)9-2-3/h3-4H,1-2,6H2,(H,7,8)/t3-,4+/m0/s1	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
					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 InChI=1S/C7H11NO2/c8-6-3-1-2-5(4-6)7(9)10/h1,3,5-6H,2,4,8H2,(H,9,10)/t5-,6+/m0/s1	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
					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 InChI=1S/C6H11NO2/c1-2-5(7)3-4-6(8)9/h2,5H,1,3-4,7H2,(H,8,9)	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
					More data for this Ligand-Target Pair
4-aminobutyrate aminotransferase, mitochondrial (Homo sapiens (Human))	BDBM323801 ((4S)-4-Aminotetrahydrothiophene-2-carboxylic acid ...) Show SMILES [NH3+][C@H]1C[C@H](C([O-])=O)S(=O)(=O)C1 Show InChI InChI=1S/C5H9NO4S/c6-3-1-4(5(7)8)11(9,10)2-3/h3-4H,1-2,6H2,(H,7,8)/t3-,4+/m0/s1	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
					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 InChI=1S/C5H9NO4S/c6-3-1-4(5(7)8)11(9,10)2-3/h3-4H,1-2,6H2,(H,7,8)/t3-,4?/m0/s1	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
					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 InChI=1S/C6H11NO2/c1-2-5(7)3-4-6(8)9/h2,5H,1,3-4,7H2,(H,8,9)	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
					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 InChI=1S/C6H11NO2/c1-2-5(7)3-4-6(8)9/h2,5H,1,3-4,7H2,(H,8,9)/t5-/m0/s1	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
					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 InChI=1S/C5H9NO2S/c6-3-1-4(5(7)8)9-2-3/h3-4H,1-2,6H2,(H,7,8)/t3-,4+/m1/s1	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
					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 InChI=1S/C5H9NO2S/c6-3-1-4(5(7)8)9-2-3/h3-4H,1-2,6H2,(H,7,8)/t3-,4+/m1/s1	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
					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 InChI=1S/C5H9NO2S/c6-3-1-4(5(7)8)9-2-3/h3-4H,1-2,6H2,(H,7,8)/t3-,4-/m1/s1	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
					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 InChI=1S/C5H9NO2S/c6-3-1-4(5(7)8)9-2-3/h3-4H,1-2,6H2,(H,7,8)/t3-,4-/m1/s1	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
					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 InChI=1S/C7H7F2NO/c8-5-2-1-4(3-10)6(9)7(5)11/h1-2,11H,3,10H2	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
					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 InChI=1S/C7H7F2NO/c8-5-2-1-4(3-10)6(9)7(5)11/h1-2,11H,3,10H2	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 InChI=1S/C5H9NO4S/c6-3-1-4(5(7)8)11(9,10)2-3/h3-4H,1-2,6H2,(H,7,8)/t3-,4?/m1/s1	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
					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 InChI=1S/C5H9NO4S/c6-3-1-4(5(7)8)11(9,10)2-3/h3-4H,1-2,6H2,(H,7,8)/t3-,4?/m1/s1	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
					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 InChI=1S/C7H7F2NO/c8-5-1-4(3-10)2-6(9)7(5)11/h1-2,11H,3,10H2	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
					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 InChI=1S/C7H7F2NO/c8-5-1-4(3-10)2-6(9)7(5)11/h1-2,11H,3,10H2	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))	BDBM50118887 (2-Amino-cyclohex-3-enecarboxylic acid | CHEMBL1384...) Show SMILES N[C@@H]1C=CCC[C@@H]1C(O)=O |c:2| Show InChI InChI=1S/C7H11NO2/c8-6-4-2-1-3-5(6)7(9)10/h2,4-6H,1,3,8H2,(H,9,10)/t5-,6+/m0/s1	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
					More data for this Ligand-Target Pair