Compile Data Set for Download or QSAR

Found 10 hits Enz. Inhib. hit(s) with Target = 'Tyrosine aminotransferase'   

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
Tyrosine aminotransferase (Rattus norvegicus)	BDBM50272493 ((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...) Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC(C)(C)CC(C)(C)C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C31H46FNO6/c1-18-13-22-21-10-9-19-14-20(35)11-12-28(19,7)30(21,32)23(36)15-29(22,8)31(18,24(37)16-34)39-25(38)33-27(5,6)17-26(2,3)4/h11-12,14,18,21-23,34,36H,9-10,13,15-17H2,1-8H3,(H,33,38)/t18-,21-,22-,23-,28-,29-,30-,31-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	156	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells				Bioorg Med Chem 16: 7535-42 (2008) Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX
					More data for this Ligand-Target Pair
Tyrosine aminotransferase (Rattus norvegicus)	BDBM50272400 ((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...) Show SMILES CCCCCNC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:21,t:17| Show InChI InChI=1S/C28H40FNO6/c1-5-6-7-12-30-24(35)36-28(23(34)16-31)17(2)13-21-20-9-8-18-14-19(32)10-11-25(18,3)27(20,29)22(33)15-26(21,28)4/h10-11,14,17,20-22,31,33H,5-9,12-13,15-16H2,1-4H3,(H,30,35)/t17-,20-,21-,22-,25-,26-,27-,28-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	117	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells				Bioorg Med Chem 16: 7535-42 (2008) Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX
					More data for this Ligand-Target Pair
Tyrosine aminotransferase (Rattus norvegicus)	BDBM50272434 ((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...) Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC(C)(C)C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C27H38FNO6/c1-15-11-19-18-8-7-16-12-17(31)9-10-24(16,5)26(18,28)20(32)13-25(19,6)27(15,21(33)14-30)35-22(34)29-23(2,3)4/h9-10,12,15,18-20,30,32H,7-8,11,13-14H2,1-6H3,(H,29,34)/t15-,18-,19-,20-,24-,25-,26-,27-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	5.30	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells				Bioorg Med Chem 16: 7535-42 (2008) Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX
					More data for this Ligand-Target Pair
Tyrosine aminotransferase (Rattus norvegicus)	BDBM50272435 ((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...) Show SMILES COC(=O)[C@H](C)NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:22,t:18| Show InChI InChI=1S/C27H36FNO8/c1-14-10-19-18-7-6-16-11-17(31)8-9-24(16,3)26(18,28)20(32)12-25(19,4)27(14,21(33)13-30)37-23(35)29-15(2)22(34)36-5/h8-9,11,14-15,18-20,30,32H,6-7,10,12-13H2,1-5H3,(H,29,35)/t14-,15-,18-,19-,20-,24-,25-,26-,27-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	211	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells				Bioorg Med Chem 16: 7535-42 (2008) Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX
					More data for this Ligand-Target Pair
Tyrosine aminotransferase (Rattus norvegicus)	BDBM50272492 ((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...) Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NCCC(C)(C)C)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C29H42FNO6/c1-17-13-21-20-8-7-18-14-19(33)9-10-26(18,5)28(20,30)22(34)15-27(21,6)29(17,23(35)16-32)37-24(36)31-12-11-25(2,3)4/h9-10,14,17,20-22,32,34H,7-8,11-13,15-16H2,1-6H3,(H,31,36)/t17-,20-,21-,22-,26-,27-,28-,29-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	646	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells				Bioorg Med Chem 16: 7535-42 (2008) Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX
					More data for this Ligand-Target Pair
Tyrosine aminotransferase (Rattus norvegicus)	BDBM50272523 ((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...) Show SMILES C[C@H](NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO)c1ccccc1 |r,c:18,t:14| Show InChI InChI=1S/C31H38FNO6/c1-18-14-24-23-11-10-21-15-22(35)12-13-28(21,3)30(23,32)25(36)16-29(24,4)31(18,26(37)17-34)39-27(38)33-19(2)20-8-6-5-7-9-20/h5-9,12-13,15,18-19,23-25,34,36H,10-11,14,16-17H2,1-4H3,(H,33,38)/t18-,19-,23-,24-,25-,28-,29-,30-,31-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	37.3	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells				Bioorg Med Chem 16: 7535-42 (2008) Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX
					More data for this Ligand-Target Pair
Tyrosine aminotransferase (Rattus norvegicus)	BDBM50272522 ((11beta,16beta)-9-Fluoro-11,21-dihydroxy-16-methyl...) Show SMILES C[C@@H](NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO)c1ccccc1 |r,c:18,t:14| Show InChI InChI=1S/C31H38FNO6/c1-18-14-24-23-11-10-21-15-22(35)12-13-28(21,3)30(23,32)25(36)16-29(24,4)31(18,26(37)17-34)39-27(38)33-19(2)20-8-6-5-7-9-20/h5-9,12-13,15,18-19,23-25,34,36H,10-11,14,16-17H2,1-4H3,(H,33,38)/t18-,19+,23-,24-,25-,28-,29-,30-,31-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	70.3	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells				Bioorg Med Chem 16: 7535-42 (2008) Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX
					More data for this Ligand-Target Pair
Tyrosine aminotransferase (Rattus norvegicus)	BDBM50272521 (Adamantan-1-yl-carbamic acid (8S,9R,10S,11S,13S,14...) Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC12CC3CC(CC(C3)C1)C2)C(=O)CO |r,c:11,t:7,TLB:26:27:30.29.34:32,THB:28:29:32:36.27.35,28:27:30.29.34:32,35:27:30:34.33.32,35:33:30:36.28.27,26:27:30:34.33.32| Show InChI InChI=1S/C33H44FNO6/c1-18-8-25-24-5-4-22-12-23(37)6-7-29(22,2)32(24,34)26(38)16-30(25,3)33(18,27(39)17-36)41-28(40)35-31-13-19-9-20(14-31)11-21(10-19)15-31/h6-7,12,18-21,24-26,36,38H,4-5,8-11,13-17H2,1-3H3,(H,35,40)/t18-,19?,20?,21?,24-,25-,26-,29-,30-,31?,32-,33-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	9.80	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells				Bioorg Med Chem 16: 7535-42 (2008) Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX
					More data for this Ligand-Target Pair
Tyrosine aminotransferase (Rattus norvegicus)	BDBM50272520 ((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...) Show SMILES C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(=O)NC1CCCCC1)C(=O)CO |r,c:11,t:7| Show InChI InChI=1S/C29H40FNO6/c1-17-13-22-21-10-9-18-14-20(33)11-12-26(18,2)28(21,30)23(34)15-27(22,3)29(17,24(35)16-32)37-25(36)31-19-7-5-4-6-8-19/h11-12,14,17,19,21-23,32,34H,4-10,13,15-16H2,1-3H3,(H,31,36)/t17-,21-,22-,23-,26-,27-,28-,29-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	2	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells				Bioorg Med Chem 16: 7535-42 (2008) Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX
					More data for this Ligand-Target Pair
Tyrosine aminotransferase (Rattus norvegicus)	BDBM50272469 ((8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydrox...) Show SMILES CCC(C)(C)NC(=O)O[C@@]1([C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C)C(=O)CO |r,c:21,t:17| Show InChI InChI=1S/C28H40FNO6/c1-7-24(3,4)30-23(35)36-28(22(34)15-31)16(2)12-20-19-9-8-17-13-18(32)10-11-25(17,5)27(19,29)21(33)14-26(20,28)6/h10-11,13,16,19-21,31,33H,7-9,12,14-15H2,1-6H3,(H,30,35)/t16-,19-,20-,21-,25-,26-,27-,28-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	705	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Transactivation activity of tyrosine amino transferase in rat H4 cells				Bioorg Med Chem 16: 7535-42 (2008) Article DOI: 10.1016/j.bmc.2008.07.037 BindingDB Entry DOI: 10.7270/Q2CC10HX
					More data for this Ligand-Target Pair