Compile Data Set for Download or QSAR

Found 190 hits with Last Name = 'dixon' and Initial = 's'   

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
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50200013 (2-(3-(((S)-6-((S)-1-amino-3-(3-chlorophenyl)-1-oxo...) Show SMILES Cc1ccc(C(=O)N[C@@H](CCCCNC(=O)c2cccc(OCC(O)=O)c2)C(=O)N[C@@H](Cc2cccc(Cl)c2)C(N)=O)c(c1O)[N+]([O-])=O |r| Show InChI InChI=1S/C32H34ClN5O10/c1-18-11-12-23(27(28(18)41)38(46)47)31(44)36-24(32(45)37-25(29(34)42)15-19-6-4-8-21(33)14-19)10-2-3-13-35-30(43)20-7-5-9-22(16-20)48-17-26(39)40/h4-9,11-12,14,16,24-25,41H,2-3,10,13,15,17H2,1H3,(H2,34,42)(H,35,43)(H,36,44)(H,37,45)(H,39,40)/t24-,25-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50317145 (2-(3-((S)-5-((S)-1-amino-3-(4-cyanophenyl)-1-oxopr...) Show SMILES Cc1ccc(C(=O)N[C@@H](CCCNC(=O)c2cccc(OCC(O)=O)c2)C(=O)N[C@@H](Cc2ccc(cc2)C#N)C(N)=O)c(c1O)[N+]([O-])=O |r| Show InChI InChI=1S/C32H32N6O10/c1-18-7-12-23(27(28(18)41)38(46)47)31(44)36-24(32(45)37-25(29(34)42)14-19-8-10-20(16-33)11-9-19)6-3-13-35-30(43)21-4-2-5-22(15-21)48-17-26(39)40/h2,4-5,7-12,15,24-25,41H,3,6,13-14,17H2,1H3,(H2,34,42)(H,35,43)(H,36,44)(H,37,45)(H,39,40)/t24-,25-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.80E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50317147 (2-(3-(-(S)-5-((S)-1-Amino-3-(3-chlorophenyl)-1-oxo...) Show SMILES Cc1ccc(C(=O)N[C@@H](CCCNC(=O)c2cccc(OCC(O)=O)c2)C(=O)N[C@@H](Cc2cccc(Cl)c2)C(N)=O)c(c1O)[N+]([O-])=O |r| Show InChI InChI=1S/C31H32ClN5O10/c1-17-10-11-22(26(27(17)40)37(45)46)30(43)35-23(31(44)36-24(28(33)41)14-18-5-2-7-20(32)13-18)9-4-12-34-29(42)19-6-3-8-21(15-19)47-16-25(38)39/h2-3,5-8,10-11,13,15,23-24,40H,4,9,12,14,16H2,1H3,(H2,33,41)(H,34,42)(H,35,43)(H,36,44)(H,38,39)/t23-,24-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.10E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50200013 (2-(3-(((S)-6-((S)-1-amino-3-(3-chlorophenyl)-1-oxo...) Show SMILES Cc1ccc(C(=O)N[C@@H](CCCCNC(=O)c2cccc(OCC(O)=O)c2)C(=O)N[C@@H](Cc2cccc(Cl)c2)C(N)=O)c(c1O)[N+]([O-])=O |r| Show InChI InChI=1S/C32H34ClN5O10/c1-18-11-12-23(27(28(18)41)38(46)47)31(44)36-24(32(45)37-25(29(34)42)15-19-6-4-8-21(33)14-19)10-2-3-13-35-30(43)20-7-5-9-22(16-20)48-17-26(39)40/h4-9,11-12,14,16,24-25,41H,2-3,10,13,15,17H2,1H3,(H2,34,42)(H,35,43)(H,36,44)(H,37,45)(H,39,40)/t24-,25-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.40E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Isochorismate synthase EntC (Escherichia coli (strain K12))	BDBM50317142 (2-(3-((S)-5-((S)-1-amino-3-(3-hydroxy-4-nitropheny...) Show SMILES COc1cc(OC)cc(c1)C(=O)N[C@@H](CCCNC(=O)c1cccc(OCC(O)=O)c1)C(=O)N[C@@H](Cc1ccc(c(O)c1)[N+]([O-])=O)C(N)=O |r| Show InChI InChI=1S/C32H35N5O12/c1-47-22-14-20(15-23(16-22)48-2)31(43)35-24(7-4-10-34-30(42)19-5-3-6-21(13-19)49-17-28(39)40)32(44)36-25(29(33)41)11-18-8-9-26(37(45)46)27(38)12-18/h3,5-6,8-9,12-16,24-25,38H,4,7,10-11,17H2,1-2H3,(H2,33,41)(H,34,42)(H,35,43)(H,36,44)(H,39,40)/t24-,25-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.60E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 IS expressed in Escherichia coli BL21(DE3) by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50317142 (2-(3-((S)-5-((S)-1-amino-3-(3-hydroxy-4-nitropheny...) Show SMILES COc1cc(OC)cc(c1)C(=O)N[C@@H](CCCNC(=O)c1cccc(OCC(O)=O)c1)C(=O)N[C@@H](Cc1ccc(c(O)c1)[N+]([O-])=O)C(N)=O |r| Show InChI InChI=1S/C32H35N5O12/c1-47-22-14-20(15-23(16-22)48-2)31(43)35-24(7-4-10-34-30(42)19-5-3-6-21(13-19)49-17-28(39)40)32(44)36-25(29(33)41)11-18-8-9-26(37(45)46)27(38)12-18/h3,5-6,8-9,12-16,24-25,38H,4,7,10-11,17H2,1-2H3,(H2,33,41)(H,34,42)(H,35,43)(H,36,44)(H,39,40)/t24-,25-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	8.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50317145 (2-(3-((S)-5-((S)-1-amino-3-(4-cyanophenyl)-1-oxopr...) Show SMILES Cc1ccc(C(=O)N[C@@H](CCCNC(=O)c2cccc(OCC(O)=O)c2)C(=O)N[C@@H](Cc2ccc(cc2)C#N)C(N)=O)c(c1O)[N+]([O-])=O |r| Show InChI InChI=1S/C32H32N6O10/c1-18-7-12-23(27(28(18)41)38(46)47)31(44)36-24(32(45)37-25(29(34)42)14-19-8-10-20(16-33)11-9-19)6-3-13-35-30(43)21-4-2-5-22(15-21)48-17-26(39)40/h2,4-5,7-12,15,24-25,41H,3,6,13-14,17H2,1H3,(H2,34,42)(H,35,43)(H,36,44)(H,37,45)(H,39,40)/t24-,25-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	8.10E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50317149 (2-(3-(3-((R)-3-((S)-1-Amino-3-(3-chlorophenyl)-1-o...) Show SMILES Cc1ccc(C(=O)N[C@@H](CSCCCNC(=O)c2cccc(OCC(O)=O)c2)C(=O)N[C@@H](Cc2cccc(Cl)c2)C(N)=O)c(c1O)[N+]([O-])=O |r| Show InChI InChI=1S/C32H34ClN5O10S/c1-18-9-10-23(27(28(18)41)38(46)47)31(44)37-25(32(45)36-24(29(34)42)14-19-5-2-7-21(33)13-19)17-49-12-4-11-35-30(43)20-6-3-8-22(15-20)48-16-26(39)40/h2-3,5-10,13,15,24-25,41H,4,11-12,14,16-17H2,1H3,(H2,34,42)(H,35,43)(H,36,45)(H,37,44)(H,39,40)/t24-,25-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9.60E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50317141 (2-(3-((4S)-5-(2-(6-(3-amino-3-oxopropyl)dibenzo[b,...) Show SMILES CC(C(=O)N[C@@H](CCCNC(=O)c1cccc(OCC(O)=O)c1)C(=O)NCCc1cccc2c3cccc(CCC(N)=O)c3oc12)c1ccc(cc1)[N+]([O-])=O |r| Show InChI InChI=1S/C40H41N5O10/c1-24(25-13-16-29(17-14-25)45(52)53)38(49)44-33(12-5-20-42-39(50)28-8-2-9-30(22-28)54-23-35(47)48)40(51)43-21-19-27-7-4-11-32-31-10-3-6-26(15-18-34(41)46)36(31)55-37(27)32/h2-4,6-11,13-14,16-17,22,24,33H,5,12,15,18-21,23H2,1H3,(H2,41,46)(H,42,50)(H,43,51)(H,44,49)(H,47,48)/t24?,33-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.10E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50317150 (CHEMBL1088356 | N-((S)-6-Amino-1-((S)-1-amino-3-(3...) Show SMILES Cc1ccc(C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc2cccc(Cl)c2)C(N)=O)c(c1O)[N+]([O-])=O |r| Show InChI InChI=1S/C23H28ClN5O6/c1-13-8-9-16(19(20(13)30)29(34)35)22(32)27-17(7-2-3-10-25)23(33)28-18(21(26)31)12-14-5-4-6-15(24)11-14/h4-6,8-9,11,17-18,30H,2-3,7,10,12,25H2,1H3,(H2,26,31)(H,27,32)(H,28,33)/t17-,18-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.10E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Isochorismate synthase EntC (Escherichia coli (strain K12))	BDBM50317149 (2-(3-(3-((R)-3-((S)-1-Amino-3-(3-chlorophenyl)-1-o...) Show SMILES Cc1ccc(C(=O)N[C@@H](CSCCCNC(=O)c2cccc(OCC(O)=O)c2)C(=O)N[C@@H](Cc2cccc(Cl)c2)C(N)=O)c(c1O)[N+]([O-])=O |r| Show InChI InChI=1S/C32H34ClN5O10S/c1-18-9-10-23(27(28(18)41)38(46)47)31(44)37-25(32(45)36-24(29(34)42)14-19-5-2-7-21(33)13-19)17-49-12-4-11-35-30(43)20-6-3-8-22(15-20)48-16-26(39)40/h2-3,5-10,13,15,24-25,41H,4,11-12,14,16-17H2,1H3,(H2,34,42)(H,35,43)(H,36,45)(H,37,44)(H,39,40)/t24-,25-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.50E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 IS expressed in Escherichia coli BL21(DE3) by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50317143 ((S)-2-(3-(5-(1-carbamoylcyclohexylamino)-4-(3,5-di...) Show SMILES NC(=O)C1(CCCCC1)NC(=O)[C@H](CCCNC(=O)c1cccc(OCC(O)=O)c1)NC(=O)c1cc(O)cc(O)c1 |r| Show InChI InChI=1S/C28H34N4O9/c29-27(40)28(9-2-1-3-10-28)32-26(39)22(31-25(38)18-12-19(33)15-20(34)13-18)8-5-11-30-24(37)17-6-4-7-21(14-17)41-16-23(35)36/h4,6-7,12-15,22,33-34H,1-3,5,8-11,16H2,(H2,29,40)(H,30,37)(H,31,38)(H,32,39)(H,35,36)/t22-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.60E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Isochorismate synthase EntC (Escherichia coli (strain K12))	BDBM50317144 (CHEMBL1094071 | {3-[(S)-4-(4-Carbamoyl-1,1-dioxo-h...) Show SMILES NC(=O)C1(CCS(=O)(=O)CC1)NC(=O)[C@H](CCCNC(=O)c1cccc(OCC(O)=O)c1)NC(=O)c1ccc(Oc2ccccc2)cc1 |r| Show InChI InChI=1S/C33H36N4O10S/c34-32(43)33(15-18-48(44,45)19-16-33)37-31(42)27(10-5-17-35-29(40)23-6-4-9-26(20-23)46-21-28(38)39)36-30(41)22-11-13-25(14-12-22)47-24-7-2-1-3-8-24/h1-4,6-9,11-14,20,27H,5,10,15-19,21H2,(H2,34,43)(H,35,40)(H,36,41)(H,37,42)(H,38,39)/t27-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.70E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 IS expressed in Escherichia coli BL21(DE3) by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Isochorismate synthase EntC (Escherichia coli (strain K12))	BDBM50317141 (2-(3-((4S)-5-(2-(6-(3-amino-3-oxopropyl)dibenzo[b,...) Show SMILES CC(C(=O)N[C@@H](CCCNC(=O)c1cccc(OCC(O)=O)c1)C(=O)NCCc1cccc2c3cccc(CCC(N)=O)c3oc12)c1ccc(cc1)[N+]([O-])=O |r| Show InChI InChI=1S/C40H41N5O10/c1-24(25-13-16-29(17-14-25)45(52)53)38(49)44-33(12-5-20-42-39(50)28-8-2-9-30(22-28)54-23-35(47)48)40(51)43-21-19-27-7-4-11-32-31-10-3-6-26(15-18-34(41)46)36(31)55-37(27)32/h2-4,6-11,13-14,16-17,22,24,33H,5,12,15,18-21,23H2,1H3,(H2,41,46)(H,42,50)(H,43,51)(H,44,49)(H,47,48)/t24?,33-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.90E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 IS expressed in Escherichia coli BL21(DE3) by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50317148 (CHEMBL1094717 | N-((S)-1-((S)-1-Amino-3-(3-chlorop...) Show SMILES C[C@H](NC(=O)c1ccc(C)c(O)c1[N+]([O-])=O)C(=O)N[C@@H](Cc1cccc(Cl)c1)C(N)=O |r| Show InChI InChI=1S/C20H21ClN4O6/c1-10-6-7-14(16(17(10)26)25(30)31)20(29)23-11(2)19(28)24-15(18(22)27)9-12-4-3-5-13(21)8-12/h3-8,11,15,26H,9H2,1-2H3,(H2,22,27)(H,23,29)(H,24,28)/t11-,15-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50200003 (3-(carboxymethoxy)benzoic acid | CHEMBL216545) Show SMILES OC(=O)COc1cccc(c1)C(O)=O Show InChI InChI=1S/C9H8O5/c10-8(11)5-14-7-3-1-2-6(4-7)9(12)13/h1-4H,5H2,(H,10,11)(H,12,13)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	2.10E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Isochorismate synthase EntC (Escherichia coli (strain K12))	BDBM50200013 (2-(3-(((S)-6-((S)-1-amino-3-(3-chlorophenyl)-1-oxo...) Show SMILES Cc1ccc(C(=O)N[C@@H](CCCCNC(=O)c2cccc(OCC(O)=O)c2)C(=O)N[C@@H](Cc2cccc(Cl)c2)C(N)=O)c(c1O)[N+]([O-])=O |r| Show InChI InChI=1S/C32H34ClN5O10/c1-18-11-12-23(27(28(18)41)38(46)47)31(44)36-24(32(45)37-25(29(34)42)15-19-6-4-8-21(33)14-19)10-2-3-13-35-30(43)20-7-5-9-22(16-20)48-17-26(39)40/h4-9,11-12,14,16,24-25,41H,2-3,10,13,15,17H2,1H3,(H2,34,42)(H,35,43)(H,36,44)(H,37,45)(H,39,40)/t24-,25-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.10E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 IS expressed in Escherichia coli BL21(DE3) by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50317141 (2-(3-((4S)-5-(2-(6-(3-amino-3-oxopropyl)dibenzo[b,...) Show SMILES CC(C(=O)N[C@@H](CCCNC(=O)c1cccc(OCC(O)=O)c1)C(=O)NCCc1cccc2c3cccc(CCC(N)=O)c3oc12)c1ccc(cc1)[N+]([O-])=O |r| Show InChI InChI=1S/C40H41N5O10/c1-24(25-13-16-29(17-14-25)45(52)53)38(49)44-33(12-5-20-42-39(50)28-8-2-9-30(22-28)54-23-35(47)48)40(51)43-21-19-27-7-4-11-32-31-10-3-6-26(15-18-34(41)46)36(31)55-37(27)32/h2-4,6-11,13-14,16-17,22,24,33H,5,12,15,18-21,23H2,1H3,(H2,41,46)(H,42,50)(H,43,51)(H,44,49)(H,47,48)/t24?,33-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.50E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Isochorismate synthase EntC (Escherichia coli (strain K12))	BDBM50317145 (2-(3-((S)-5-((S)-1-amino-3-(4-cyanophenyl)-1-oxopr...) Show SMILES Cc1ccc(C(=O)N[C@@H](CCCNC(=O)c2cccc(OCC(O)=O)c2)C(=O)N[C@@H](Cc2ccc(cc2)C#N)C(N)=O)c(c1O)[N+]([O-])=O |r| Show InChI InChI=1S/C32H32N6O10/c1-18-7-12-23(27(28(18)41)38(46)47)31(44)36-24(32(45)37-25(29(34)42)14-19-8-10-20(16-33)11-9-19)6-3-13-35-30(43)21-4-2-5-22(15-21)48-17-26(39)40/h2,4-5,7-12,15,24-25,41H,3,6,13-14,17H2,1H3,(H2,34,42)(H,35,43)(H,36,44)(H,37,45)(H,39,40)/t24-,25-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.60E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 IS expressed in Escherichia coli BL21(DE3) by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Serine racemase (Homo sapiens (Human))	BDBM50185232 ((S)-2-((S)-3-(1H-imidazol-4-yl)-2-(3-phenylpropana...) Show SMILES NC(=O)[C@H](CCc1ccccc1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CCc1ccccc1 Show InChI InChI=1S/C25H29N5O3/c26-24(32)21(13-11-18-7-3-1-4-8-18)30-25(33)22(15-20-16-27-17-28-20)29-23(31)14-12-19-9-5-2-6-10-19/h1-10,16-17,21-22H,11-15H2,(H2,26,32)(H,27,28)(H,29,31)(H,30,33)/t21-,22-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.20E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of human serine racemase				J Med Chem 49: 2388-97 (2006) Article DOI: 10.1021/jm050701c BindingDB Entry DOI: 10.7270/Q2V124C2
					More data for this Ligand-Target Pair
Isochorismate synthase EntC (Escherichia coli (strain K12))	BDBM50317147 (2-(3-(-(S)-5-((S)-1-Amino-3-(3-chlorophenyl)-1-oxo...) Show SMILES Cc1ccc(C(=O)N[C@@H](CCCNC(=O)c2cccc(OCC(O)=O)c2)C(=O)N[C@@H](Cc2cccc(Cl)c2)C(N)=O)c(c1O)[N+]([O-])=O |r| Show InChI InChI=1S/C31H32ClN5O10/c1-17-10-11-22(26(27(17)40)37(45)46)30(43)35-23(31(44)36-24(28(33)41)14-18-5-2-7-20(32)13-18)9-4-12-34-29(42)19-6-3-8-21(15-19)47-16-25(38)39/h2-3,5-8,10-11,13,15,23-24,40H,4,9,12,14,16H2,1H3,(H2,33,41)(H,34,42)(H,35,43)(H,36,44)(H,38,39)/t23-,24-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.60E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 IS expressed in Escherichia coli BL21(DE3) by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50317143 ((S)-2-(3-(5-(1-carbamoylcyclohexylamino)-4-(3,5-di...) Show SMILES NC(=O)C1(CCCCC1)NC(=O)[C@H](CCCNC(=O)c1cccc(OCC(O)=O)c1)NC(=O)c1cc(O)cc(O)c1 |r| Show InChI InChI=1S/C28H34N4O9/c29-27(40)28(9-2-1-3-10-28)32-26(39)22(31-25(38)18-12-19(33)15-20(34)13-18)8-5-11-30-24(37)17-6-4-7-21(14-17)41-16-23(35)36/h4,6-7,12-15,22,33-34H,1-3,5,8-11,16H2,(H2,29,40)(H,30,37)(H,31,38)(H,32,39)(H,35,36)/t22-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.89E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Isochorismate synthase EntC (Escherichia coli (strain K12))	BDBM50317146 ((S)-2-(3-(4-(3-benzoylpicolinamido)-5-(1-carbamoyl...) Show SMILES NC(=O)C1(CCCCC1)NC(=O)[C@H](CCCNC(=O)c1cccc(OCC(O)=O)c1)NC(=O)c1ncccc1C(=O)c1ccccc1 |r| Show InChI InChI=1S/C34H37N5O8/c35-33(46)34(16-5-2-6-17-34)39-31(44)26(15-9-19-37-30(43)23-12-7-13-24(20-23)47-21-27(40)41)38-32(45)28-25(14-8-18-36-28)29(42)22-10-3-1-4-11-22/h1,3-4,7-8,10-14,18,20,26H,2,5-6,9,15-17,19,21H2,(H2,35,46)(H,37,43)(H,38,45)(H,39,44)(H,40,41)/t26-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.30E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 IS expressed in Escherichia coli BL21(DE3) by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50317146 ((S)-2-(3-(4-(3-benzoylpicolinamido)-5-(1-carbamoyl...) Show SMILES NC(=O)C1(CCCCC1)NC(=O)[C@H](CCCNC(=O)c1cccc(OCC(O)=O)c1)NC(=O)c1ncccc1C(=O)c1ccccc1 |r| Show InChI InChI=1S/C34H37N5O8/c35-33(46)34(16-5-2-6-17-34)39-31(44)26(15-9-19-37-30(43)23-12-7-13-24(20-23)47-21-27(40)41)38-32(45)28-25(14-8-18-36-28)29(42)22-10-3-1-4-11-22/h1,3-4,7-8,10-14,18,20,26H,2,5-6,9,15-17,19,21H2,(H2,35,46)(H,37,43)(H,38,45)(H,39,44)(H,40,41)/t26-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.90E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Isochorismate synthase EntC (Escherichia coli (strain K12))	BDBM50317148 (CHEMBL1094717 | N-((S)-1-((S)-1-Amino-3-(3-chlorop...) Show SMILES C[C@H](NC(=O)c1ccc(C)c(O)c1[N+]([O-])=O)C(=O)N[C@@H](Cc1cccc(Cl)c1)C(N)=O |r| Show InChI InChI=1S/C20H21ClN4O6/c1-10-6-7-14(16(17(10)26)25(30)31)20(29)23-11(2)19(28)24-15(18(22)27)9-12-4-3-5-13(21)8-12/h3-8,11,15,26H,9H2,1-2H3,(H2,22,27)(H,23,29)(H,24,28)/t11-,15-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 IS expressed in Escherichia coli BL21(DE3) by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50200003 (3-(carboxymethoxy)benzoic acid | CHEMBL216545) Show SMILES OC(=O)COc1cccc(c1)C(O)=O Show InChI InChI=1S/C9H8O5/c10-8(11)5-14-7-3-1-2-6(4-7)9(12)13/h1-4H,5H2,(H,10,11)(H,12,13)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	5.50E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50317144 (CHEMBL1094071 | {3-[(S)-4-(4-Carbamoyl-1,1-dioxo-h...) Show SMILES NC(=O)C1(CCS(=O)(=O)CC1)NC(=O)[C@H](CCCNC(=O)c1cccc(OCC(O)=O)c1)NC(=O)c1ccc(Oc2ccccc2)cc1 |r| Show InChI InChI=1S/C33H36N4O10S/c34-32(43)33(15-18-48(44,45)19-16-33)37-31(42)27(10-5-17-35-29(40)23-6-4-9-26(20-23)46-21-28(38)39)36-30(41)22-11-13-25(14-12-22)47-24-7-2-1-3-8-24/h1-4,6-9,11-14,20,27H,5,10,15-19,21H2,(H2,34,43)(H,35,40)(H,36,41)(H,37,42)(H,38,39)/t27-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.70E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Serine racemase (Homo sapiens (Human))	BDBM50185231 ((2S,3R)-2-((S)-3-(1H-imidazol-4-yl)-2-(3-phenylpro...) Show SMILES CCC(C)[C@H](NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CCc1ccccc1)C(N)=O Show InChI InChI=1S/C21H29N5O3/c1-3-14(2)19(20(22)28)26-21(29)17(11-16-12-23-13-24-16)25-18(27)10-9-15-7-5-4-6-8-15/h4-8,12-14,17,19H,3,9-11H2,1-2H3,(H2,22,28)(H,23,24)(H,25,27)(H,26,29)/t14?,17-,19-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.10E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of human serine racemase				J Med Chem 49: 2388-97 (2006) Article DOI: 10.1021/jm050701c BindingDB Entry DOI: 10.7270/Q2V124C2
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50200006 (2-(3-carbamoylphenoxy)acetic acid | CHEMBL216601 |...) Show SMILES NC(=O)c1cccc(OCC(O)=O)c1 Show InChI InChI=1S/C9H9NO4/c10-9(13)6-2-1-3-7(4-6)14-5-8(11)12/h1-4H,5H2,(H2,10,13)(H,11,12)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents	Article PubMed	7.60E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Aminodeoxychorismate lyase (Escherichia coli (strain K12))	BDBM50200013 (2-(3-(((S)-6-((S)-1-amino-3-(3-chlorophenyl)-1-oxo...) Show SMILES Cc1ccc(C(=O)N[C@@H](CCCCNC(=O)c2cccc(OCC(O)=O)c2)C(=O)N[C@@H](Cc2cccc(Cl)c2)C(N)=O)c(c1O)[N+]([O-])=O |r| Show InChI InChI=1S/C32H34ClN5O10/c1-18-11-12-23(27(28(18)41)38(46)47)31(44)36-24(32(45)37-25(29(34)42)15-19-6-4-8-21(33)14-19)10-2-3-13-35-30(43)20-7-5-9-22(16-20)48-17-26(39)40/h4-9,11-12,14,16,24-25,41H,2-3,10,13,15,17H2,1H3,(H2,34,42)(H,35,43)(H,36,44)(H,37,45)(H,39,40)/t24-,25-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.70E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 ADCS by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Isochorismate synthase EntC (Escherichia coli (strain K12))	BDBM50317150 (CHEMBL1088356 | N-((S)-6-Amino-1-((S)-1-amino-3-(3...) Show SMILES Cc1ccc(C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc2cccc(Cl)c2)C(N)=O)c(c1O)[N+]([O-])=O |r| Show InChI InChI=1S/C23H28ClN5O6/c1-13-8-9-16(19(20(13)30)29(34)35)22(32)27-17(7-2-3-10-25)23(33)28-18(21(26)31)12-14-5-4-6-15(24)11-14/h4-6,8-9,11,17-18,30H,2-3,7,10,12,25H2,1H3,(H2,26,31)(H,27,32)(H,28,33)/t17-,18-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.90E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 IS expressed in Escherichia coli BL21(DE3) by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Aminodeoxychorismate lyase (Escherichia coli (strain K12))	BDBM50317147 (2-(3-(-(S)-5-((S)-1-Amino-3-(3-chlorophenyl)-1-oxo...) Show SMILES Cc1ccc(C(=O)N[C@@H](CCCNC(=O)c2cccc(OCC(O)=O)c2)C(=O)N[C@@H](Cc2cccc(Cl)c2)C(N)=O)c(c1O)[N+]([O-])=O |r| Show InChI InChI=1S/C31H32ClN5O10/c1-17-10-11-22(26(27(17)40)37(45)46)30(43)35-23(31(44)36-24(28(33)41)14-18-5-2-7-20(32)13-18)9-4-12-34-29(42)19-6-3-8-21(15-19)47-16-25(38)39/h2-3,5-8,10-11,13,15,23-24,40H,4,9,12,14,16H2,1H3,(H2,33,41)(H,34,42)(H,35,43)(H,36,44)(H,38,39)/t23-,24-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 ADCS by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50317144 (CHEMBL1094071 | {3-[(S)-4-(4-Carbamoyl-1,1-dioxo-h...) Show SMILES NC(=O)C1(CCS(=O)(=O)CC1)NC(=O)[C@H](CCCNC(=O)c1cccc(OCC(O)=O)c1)NC(=O)c1ccc(Oc2ccccc2)cc1 |r| Show InChI InChI=1S/C33H36N4O10S/c34-32(43)33(15-18-48(44,45)19-16-33)37-31(42)27(10-5-17-35-29(40)23-6-4-9-26(20-23)46-21-28(38)39)36-30(41)22-11-13-25(14-12-22)47-24-7-2-1-3-8-24/h1-4,6-9,11-14,20,27H,5,10,15-19,21H2,(H2,34,43)(H,35,40)(H,36,41)(H,37,42)(H,38,39)/t27-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.02E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50317146 ((S)-2-(3-(4-(3-benzoylpicolinamido)-5-(1-carbamoyl...) Show SMILES NC(=O)C1(CCCCC1)NC(=O)[C@H](CCCNC(=O)c1cccc(OCC(O)=O)c1)NC(=O)c1ncccc1C(=O)c1ccccc1 |r| Show InChI InChI=1S/C34H37N5O8/c35-33(46)34(16-5-2-6-17-34)39-31(44)26(15-9-19-37-30(43)23-12-7-13-24(20-23)47-21-27(40)41)38-32(45)28-25(14-8-18-36-28)29(42)22-10-3-1-4-11-22/h1,3-4,7-8,10-14,18,20,26H,2,5-6,9,15-17,19,21H2,(H2,35,46)(H,37,43)(H,38,45)(H,39,44)(H,40,41)/t26-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.08E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Isochorismate synthase EntC (Escherichia coli (strain K12))	BDBM50317143 ((S)-2-(3-(5-(1-carbamoylcyclohexylamino)-4-(3,5-di...) Show SMILES NC(=O)C1(CCCCC1)NC(=O)[C@H](CCCNC(=O)c1cccc(OCC(O)=O)c1)NC(=O)c1cc(O)cc(O)c1 |r| Show InChI InChI=1S/C28H34N4O9/c29-27(40)28(9-2-1-3-10-28)32-26(39)22(31-25(38)18-12-19(33)15-20(34)13-18)8-5-11-30-24(37)17-6-4-7-21(14-17)41-16-23(35)36/h4,6-7,12-15,22,33-34H,1-3,5,8-11,16H2,(H2,29,40)(H,30,37)(H,31,38)(H,32,39)(H,35,36)/t22-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.20E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 IS expressed in Escherichia coli BL21(DE3) by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Isochorismate synthase EntC (Escherichia coli (strain K12))	BDBM50200003 (3-(carboxymethoxy)benzoic acid | CHEMBL216545) Show SMILES OC(=O)COc1cccc(c1)C(O)=O Show InChI InChI=1S/C9H8O5/c10-8(11)5-14-7-3-1-2-6(4-7)9(12)13/h1-4H,5H2,(H,10,11)(H,12,13)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	1.30E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 IS expressed in Escherichia coli BL21(DE3) by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Aminodeoxychorismate lyase (Escherichia coli (strain K12))	BDBM50317149 (2-(3-(3-((R)-3-((S)-1-Amino-3-(3-chlorophenyl)-1-o...) Show SMILES Cc1ccc(C(=O)N[C@@H](CSCCCNC(=O)c2cccc(OCC(O)=O)c2)C(=O)N[C@@H](Cc2cccc(Cl)c2)C(N)=O)c(c1O)[N+]([O-])=O |r| Show InChI InChI=1S/C32H34ClN5O10S/c1-18-9-10-23(27(28(18)41)38(46)47)31(44)37-25(32(45)36-24(29(34)42)14-19-5-2-7-21(33)13-19)17-49-12-4-11-35-30(43)20-6-3-8-22(15-20)48-16-26(39)40/h2-3,5-10,13,15,24-25,41H,4,11-12,14,16-17H2,1H3,(H2,34,42)(H,35,43)(H,36,45)(H,37,44)(H,39,40)/t24-,25-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.50E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 ADCS by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Anthranilate synthase component 1 (Salmonella typhimurium)	BDBM50200006 (2-(3-carbamoylphenoxy)acetic acid | CHEMBL216601 |...) Show SMILES NC(=O)c1cccc(OCC(O)=O)c1 Show InChI InChI=1S/C9H9NO4/c10-9(13)6-2-1-3-7(4-6)14-5-8(11)12/h1-4H,5H2,(H2,10,13)(H,11,12)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents	Article PubMed	2.60E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Salmonella typhimurium anthranilate synthase trpE:trpD expressed in Escherichia coli BL21(DE3) coexpressing stop codon in trpD gene for...				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Isochorismate synthase EntC (Escherichia coli (strain K12))	BDBM50200006 (2-(3-carbamoylphenoxy)acetic acid | CHEMBL216601 |...) Show SMILES NC(=O)c1cccc(OCC(O)=O)c1 Show InChI InChI=1S/C9H9NO4/c10-9(13)6-2-1-3-7(4-6)14-5-8(11)12/h1-4H,5H2,(H2,10,13)(H,11,12)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents	Article PubMed	2.60E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 IS expressed in Escherichia coli BL21(DE3) by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Aminodeoxychorismate lyase (Escherichia coli (strain K12))	BDBM50317150 (CHEMBL1088356 | N-((S)-6-Amino-1-((S)-1-amino-3-(3...) Show SMILES Cc1ccc(C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc2cccc(Cl)c2)C(N)=O)c(c1O)[N+]([O-])=O |r| Show InChI InChI=1S/C23H28ClN5O6/c1-13-8-9-16(19(20(13)30)29(34)35)22(32)27-17(7-2-3-10-25)23(33)28-18(21(26)31)12-14-5-4-6-15(24)11-14/h4-6,8-9,11,17-18,30H,2-3,7,10,12,25H2,1H3,(H2,26,31)(H,27,32)(H,28,33)/t17-,18-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.70E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 ADCS by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Aminodeoxychorismate lyase (Escherichia coli (strain K12))	BDBM50317148 (CHEMBL1094717 | N-((S)-1-((S)-1-Amino-3-(3-chlorop...) Show SMILES C[C@H](NC(=O)c1ccc(C)c(O)c1[N+]([O-])=O)C(=O)N[C@@H](Cc1cccc(Cl)c1)C(N)=O |r| Show InChI InChI=1S/C20H21ClN4O6/c1-10-6-7-14(16(17(10)26)25(30)31)20(29)23-11(2)19(28)24-15(18(22)27)9-12-4-3-5-13(21)8-12/h3-8,11,15,26H,9H2,1-2H3,(H2,22,27)(H,23,29)(H,24,28)/t11-,15-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.80E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Inhibition of Escherichia coli K12 ADCS by spectrophotometry				J Med Chem 53: 3718-29 (2010) Article DOI: 10.1021/jm100158v BindingDB Entry DOI: 10.7270/Q25T3KN4
					More data for this Ligand-Target Pair
Urokinase-type plasminogen activator (Homo sapiens (Human))	BDBM50088982 (CHEMBL160253 | CHEMBL367004 | N-[1-(1-Carbamimidoy...) Show SMILES C[C@H](NC(=O)[C@@H](CO)NS(=O)(=O)CCc1ccccc1)C(=O)N[C@H]1CCCN(C1O)C(N)=N Show InChI InChI=1S/C20H32N6O6S/c1-13(17(28)24-15-8-5-10-26(19(15)30)20(21)22)23-18(29)16(12-27)25-33(31,32)11-9-14-6-3-2-4-7-14/h2-4,6-7,13,15-16,19,25,27,30H,5,8-12H2,1H3,(H3,21,22)(H,23,29)(H,24,28)/t13-,15-,16+,19?/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.10	n/a	n/a	n/a	n/a	n/a	n/a
Corvas International, Inc. Curated by ChEMBL					Assay Description The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50				Bioorg Med Chem Lett 10: 983-7 (2000) BindingDB Entry DOI: 10.7270/Q2765DKB
					More data for this Ligand-Target Pair
Urokinase-type plasminogen activator (Homo sapiens (Human))	BDBM50088978 (CHEMBL176515 | N-[1-(1-Carbamimidoyl-2-hydroxy-pip...) Show SMILES C[C@H](NC(=O)[C@@H](CO)NS(=O)(=O)Cc1ccccc1)C(=O)N[C@H]1CCCN(C1O)C(N)=N Show InChI InChI=1S/C19H30N6O6S/c1-12(16(27)23-14-8-5-9-25(18(14)29)19(20)21)22-17(28)15(10-26)24-32(30,31)11-13-6-3-2-4-7-13/h2-4,6-7,12,14-15,18,24,26,29H,5,8-11H2,1H3,(H3,20,21)(H,22,28)(H,23,27)/t12-,14-,15+,18?/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.10	n/a	n/a	n/a	n/a	n/a	n/a
Corvas International, Inc. Curated by ChEMBL					Assay Description The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50				Bioorg Med Chem Lett 10: 983-7 (2000) BindingDB Entry DOI: 10.7270/Q2765DKB
					More data for this Ligand-Target Pair
Urokinase-type plasminogen activator (Homo sapiens (Human))	BDBM50088984 (2-Benzenesulfonylamino-N-[1-(1-carbamimidoyl-2-hyd...) Show SMILES C[C@H](NC(=O)[C@@H](CO)NS(=O)(=O)c1ccccc1)C(=O)N[C@H]1CCCN(C1O)C(N)=N Show InChI InChI=1S/C18H28N6O6S/c1-11(15(26)22-13-8-5-9-24(17(13)28)18(19)20)21-16(27)14(10-25)23-31(29,30)12-6-3-2-4-7-12/h2-4,6-7,11,13-14,17,23,25,28H,5,8-10H2,1H3,(H3,19,20)(H,21,27)(H,22,26)/t11-,13-,14+,17?/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Corvas International, Inc. Curated by ChEMBL					Assay Description The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50				Bioorg Med Chem Lett 10: 983-7 (2000) BindingDB Entry DOI: 10.7270/Q2765DKB
					More data for this Ligand-Target Pair
Urokinase-type plasminogen activator (Homo sapiens (Human))	BDBM50088979 (CHEMBL366666 | {(R)-2-[2-((S)-1-Carbamimidoyl-2-hy...) Show SMILES NC(=N)N1CCC[C@H](NC(=O)C2CCN2C(=O)[C@@H](CO)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C21H30N6O6/c22-20(23)27-9-4-7-14(18(27)30)24-17(29)16-8-10-26(16)19(31)15(11-28)25-21(32)33-12-13-5-2-1-3-6-13/h1-3,5-6,14-16,18,28,30H,4,7-12H2,(H3,22,23)(H,24,29)(H,25,32)/t14-,15+,16?,18?/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	11	n/a	n/a	n/a	n/a	n/a	n/a
Corvas International, Inc. Curated by ChEMBL					Assay Description The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50				Bioorg Med Chem Lett 10: 983-7 (2000) BindingDB Entry DOI: 10.7270/Q2765DKB
					More data for this Ligand-Target Pair
Urokinase-type plasminogen activator (Homo sapiens (Human))	BDBM50088985 (CHEMBL369042 | {2-[2-(1-Carbamimidoyl-2-hydroxy-pi...) Show SMILES NC(=N)N1CCCC(NC(=O)[C@H]2CCCN2C(=O)C(CO)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C22H32N6O6/c23-21(24)28-11-4-8-15(19(28)31)25-18(30)17-9-5-10-27(17)20(32)16(12-29)26-22(33)34-13-14-6-2-1-3-7-14/h1-3,6-7,15-17,19,29,31H,4-5,8-13H2,(H3,23,24)(H,25,30)(H,26,33)/t15?,16?,17-,19?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	12	n/a	n/a	n/a	n/a	n/a	n/a
Corvas International, Inc. Curated by ChEMBL					Assay Description The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50				Bioorg Med Chem Lett 10: 983-7 (2000) BindingDB Entry DOI: 10.7270/Q2765DKB
					More data for this Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform (Mus musculus (Mouse))	BDBM217352 (GS-9820) Show SMILES C[C@H](Nc1ncnc2[nH]cnc12)c1nc2ccc(F)cc2c(=O)n1-c1ccccc1 |r| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase MCE KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	12.7	n/a	n/a	n/a	n/a	n/a	n/a
Western University					Assay Description Biochemical in vitro lipid kinase assays were performed by the SelectScreen® biochemical kinase assay service (Invitrogen Ltd.). A stock solution of ...				J Biol Chem 288: 35346-57 (2013) Article DOI: 10.1074/jbc.M113.507525 BindingDB Entry DOI: 10.7270/Q28051F7
					More data for this Ligand-Target Pair
Urokinase-type plasminogen activator (Homo sapiens (Human))	BDBM50088977 (CHEMBL177557 | {1-[1-(1-Carbamimidoyl-2-hydroxy-pi...) Show SMILES C[C@H](NC(=O)[C@@H](CO)NC(=O)OCc1ccccc1)C(=O)N[C@H]1CCCN(C1O)C(N)=N Show InChI InChI=1S/C20H30N6O6/c1-12(16(28)24-14-8-5-9-26(18(14)30)19(21)22)23-17(29)15(10-27)25-20(31)32-11-13-6-3-2-4-7-13/h2-4,6-7,12,14-15,18,27,30H,5,8-11H2,1H3,(H3,21,22)(H,23,29)(H,24,28)(H,25,31)/t12-,14-,15+,18?/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	19	n/a	n/a	n/a	n/a	n/a	n/a
Corvas International, Inc. Curated by ChEMBL					Assay Description The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50				Bioorg Med Chem Lett 10: 983-7 (2000) BindingDB Entry DOI: 10.7270/Q2765DKB
					More data for this Ligand-Target Pair
Urokinase-type plasminogen activator (Homo sapiens (Human))	BDBM50088987 (CHEMBL174813 | {1-[1-(1-Carbamimidoyl-2-hydroxy-pi...) Show SMILES CC(C)COC(=O)N[C@H](CO)C(=O)N[C@@H](C)C(=O)N[C@H]1CCCN(C1O)C(N)=N Show InChI InChI=1S/C17H32N6O6/c1-9(2)8-29-17(28)22-12(7-24)14(26)20-10(3)13(25)21-11-5-4-6-23(15(11)27)16(18)19/h9-12,15,24,27H,4-8H2,1-3H3,(H3,18,19)(H,20,26)(H,21,25)(H,22,28)/t10-,11-,12+,15?/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem	PubMed	n/a	n/a	23	n/a	n/a	n/a	n/a	n/a	n/a
Corvas International, Inc. Curated by ChEMBL					Assay Description The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50				Bioorg Med Chem Lett 10: 983-7 (2000) BindingDB Entry DOI: 10.7270/Q2765DKB
					More data for this Ligand-Target Pair
Urokinase-type plasminogen activator (Homo sapiens (Human))	BDBM50088986 (CHEMBL433809 | {2-[2-(1-Carbamimidoyl-2-hydroxy-pi...) Show SMILES NC(=N)N1CCC[C@@H](NC(=O)[C@H]2CCCCN2C(=O)[C@@H](CO)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C23H34N6O6/c24-22(25)29-12-6-9-16(20(29)32)26-19(31)18-10-4-5-11-28(18)21(33)17(13-30)27-23(34)35-14-15-7-2-1-3-8-15/h1-3,7-8,16-18,20,30,32H,4-6,9-14H2,(H3,24,25)(H,26,31)(H,27,34)/t16-,17-,18-,20?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	101	n/a	n/a	n/a	n/a	n/a	n/a
Corvas International, Inc. Curated by ChEMBL					Assay Description The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50				Bioorg Med Chem Lett 10: 983-7 (2000) BindingDB Entry DOI: 10.7270/Q2765DKB
					More data for this Ligand-Target Pair

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