Compile Data Set for Download or QSAR

Found 44 hits with Last Name = 'venkateswarlu' and Initial = 'a'   

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
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM11639 (4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyraz...) Show SMILES Cc1ccc(cc1)-c1cc(nn1-c1ccc(cc1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C17H14F3N3O2S/c1-11-2-4-12(5-3-11)15-10-16(17(18,19)20)22-23(15)13-6-8-14(9-7-13)26(21,24)25/h2-10H,1H3,(H2,21,24,25)	PDB MMDB NCI pathway 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	DrugBank PDB PubMed	n/a	n/a	36	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair				3D Structure (crystal)
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138441 (2-(hydroxymethyl)-4-(5-(4-(methylthio)phenyl)-3-(t...) Show SMILES CSc1ccc(cc1)-c1cc(nn1-c1ccc(c(CO)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C18H16F3N3O3S2/c1-28-14-5-2-11(3-6-14)15-9-17(18(19,20)21)23-24(15)13-4-7-16(29(22,26)27)12(8-13)10-25/h2-9,25H,10H2,1H3,(H2,22,26,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	235	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138454 (2-Hydroxymethyl-4-[5-(4-methoxy-phenyl)-3-trifluor...) Show SMILES COc1ccc(cc1)-c1cc(nn1-c1ccc(c(CO)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C18H16F3N3O4S/c1-28-14-5-2-11(3-6-14)15-9-17(18(19,20)21)23-24(15)13-4-7-16(29(22,26)27)12(8-13)10-25/h2-9,25H,10H2,1H3,(H2,22,26,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	365	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50452007 (CHEMBL2112872) Show SMILES CCC(=O)OCc1cc(ccc1S(N)(=O)=O)-n1nc(cc1-c1ccc(C)cc1)C(F)(F)F Show InChI InChI=1S/C21H20F3N3O4S/c1-3-20(28)31-12-15-10-16(8-9-18(15)32(25,29)30)27-17(11-19(26-27)21(22,23)24)14-6-4-13(2)5-7-14/h4-11H,3,12H2,1-2H3,(H2,25,29,30)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	570	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138444 (4-(5-(4-bromophenyl)-3-(trifluoromethyl)-1H-pyrazo...) Show SMILES NS(=O)(=O)c1ccc(cc1CO)-n1nc(cc1-c1ccc(Br)cc1)C(F)(F)F Show InChI InChI=1S/C17H13BrF3N3O3S/c18-12-3-1-10(2-4-12)14-8-16(17(19,20)21)23-24(14)13-5-6-15(28(22,26)27)11(7-13)9-25/h1-8,25H,9H2,(H2,22,26,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	592	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138447 (4-[5-(4-Chloro-phenyl)-3-trifluoromethyl-pyrazol-1...) Show SMILES NS(=O)(=O)c1ccc(cc1CO)-n1nc(cc1-c1ccc(Cl)cc1)C(F)(F)F Show InChI InChI=1S/C17H13ClF3N3O3S/c18-12-3-1-10(2-4-12)14-8-16(17(19,20)21)23-24(14)13-5-6-15(28(22,26)27)11(7-13)9-25/h1-8,25H,9H2,(H2,22,26,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	712	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138458 (2-Hydroxymethyl-4-(5-m-tolyl-3-trifluoromethyl-pyr...) Show SMILES Cc1cccc(c1)-c1cc(nn1-c1ccc(c(CO)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C18H16F3N3O3S/c1-11-3-2-4-12(7-11)15-9-17(18(19,20)21)23-24(15)14-5-6-16(28(22,26)27)13(8-14)10-25/h2-9,25H,10H2,1H3,(H2,22,26,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	728	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138452 (2-Hydroxymethyl-4-(5-p-tolyl-3-trifluoromethyl-pyr...) Show SMILES Cc1ccc(cc1)-c1cc(nn1-c1ccc(c(CO)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C18H16F3N3O3S/c1-11-2-4-12(5-3-11)15-9-17(18(19,20)21)23-24(15)14-6-7-16(28(22,26)27)13(8-14)10-25/h2-9,25H,10H2,1H3,(H2,22,26,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	760	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138460 (4-[5-(4-Ethoxy-phenyl)-3-trifluoromethyl-pyrazol-1...) Show SMILES CCOc1ccc(cc1)-c1cc(nn1-c1ccc(c(CO)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C19H18F3N3O4S/c1-2-29-15-6-3-12(4-7-15)16-10-18(19(20,21)22)24-25(16)14-5-8-17(30(23,27)28)13(9-14)11-26/h3-10,26H,2,11H2,1H3,(H2,23,27,28)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	901	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138445 (4-[5-(4-Ethyl-phenyl)-3-trifluoromethyl-pyrazol-1-...) Show SMILES CCc1ccc(cc1)-c1cc(nn1-c1ccc(c(CO)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C19H18F3N3O3S/c1-2-12-3-5-13(6-4-12)16-10-18(19(20,21)22)24-25(16)15-7-8-17(29(23,27)28)14(9-15)11-26/h3-10,26H,2,11H2,1H3,(H2,23,27,28)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.38E+3	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138459 (4-[5-(3-Chloro-phenyl)-3-trifluoromethyl-pyrazol-1...) Show SMILES NS(=O)(=O)c1ccc(cc1CO)-n1nc(cc1-c1cccc(Cl)c1)C(F)(F)F Show InChI InChI=1S/C17H13ClF3N3O3S/c18-12-3-1-2-10(6-12)14-8-16(17(19,20)21)23-24(14)13-4-5-15(28(22,26)27)11(7-13)9-25/h1-8,25H,9H2,(H2,22,26,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.95E+3	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138442 (4-[5-(4-Fluoro-phenyl)-3-trifluoromethyl-pyrazol-1...) Show SMILES NS(=O)(=O)c1ccc(cc1CO)-n1nc(cc1-c1ccc(F)cc1)C(F)(F)F Show InChI InChI=1S/C17H13F4N3O3S/c18-12-3-1-10(2-4-12)14-8-16(17(19,20)21)23-24(14)13-5-6-15(28(22,26)27)11(7-13)9-25/h1-8,25H,9H2,(H2,22,26,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.99E+3	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138455 (CHEMBL344540 | N-{5-[5-(4-Methoxy-phenyl)-3-triflu...) Show SMILES COc1ccc(cc1)-c1cc(nn1-c1ccc(c(CNC(C)=O)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C20H19F3N4O4S/c1-12(28)25-11-14-9-15(5-8-18(14)32(24,29)30)27-17(10-19(26-27)20(21,22)23)13-3-6-16(31-2)7-4-13/h3-10H,11H2,1-2H3,(H,25,28)(H2,24,29,30)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138446 (CHEMBL358122 | {2-Methanesulfonyl-5-[5-(4-methoxy-...) Show SMILES COc1ccc(cc1)-c1cc(nn1-c1ccc(c(CO)c1)S(C)(=O)=O)C(F)(F)F Show InChI InChI=1S/C19H17F3N2O4S/c1-28-15-6-3-12(4-7-15)16-10-18(19(20,21)22)23-24(16)14-5-8-17(29(2,26)27)13(9-14)11-25/h3-10,25H,11H2,1-2H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138461 (4-[5-(2-Fluoro-phenyl)-3-trifluoromethyl-pyrazol-1...) Show SMILES NS(=O)(=O)c1ccc(cc1CO)-n1nc(cc1-c1ccccc1F)C(F)(F)F Show InChI InChI=1S/C17H13F4N3O3S/c18-13-4-2-1-3-12(13)14-8-16(17(19,20)21)23-24(14)11-5-6-15(28(22,26)27)10(7-11)9-25/h1-8,25H,9H2,(H2,22,26,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138456 (2-Hydroxymethyl-4-(5-phenyl-3-trifluoromethyl-pyra...) Show SMILES NS(=O)(=O)c1ccc(cc1CO)-n1nc(cc1-c1ccccc1)C(F)(F)F Show InChI InChI=1S/C17H14F3N3O3S/c18-17(19,20)16-9-14(11-4-2-1-3-5-11)23(22-16)13-6-7-15(27(21,25)26)12(8-13)10-24/h1-9,24H,10H2,(H2,21,25,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.45E+3	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138448 (CHEMBL149781 | N-[2-Sulfamoyl-5-(5-p-tolyl-3-trifl...) Show SMILES CC(=O)NCc1cc(ccc1S(N)(=O)=O)-n1nc(cc1-c1ccc(C)cc1)C(F)(F)F Show InChI InChI=1S/C20H19F3N4O3S/c1-12-3-5-14(6-4-12)17-10-19(20(21,22)23)26-27(17)16-7-8-18(31(24,29)30)15(9-16)11-25-13(2)28/h3-10H,11H2,1-2H3,(H,25,28)(H2,24,29,30)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	4.62E+3	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138449 (CHEMBL146465 | N-{5-[5-(4-Chloro-phenyl)-3-trifluo...) Show SMILES CC(=O)NCc1cc(ccc1S(N)(=O)=O)-n1nc(cc1-c1ccc(Cl)cc1)C(F)(F)F Show InChI InChI=1S/C19H16ClF3N4O3S/c1-11(28)25-10-13-8-15(6-7-17(13)31(24,29)30)27-16(9-18(26-27)19(21,22)23)12-2-4-14(20)5-3-12/h2-9H,10H2,1H3,(H,25,28)(H2,24,29,30)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138443 (4-[5-(2-Chloro-phenyl)-3-trifluoromethyl-pyrazol-1...) Show SMILES NS(=O)(=O)c1ccc(cc1CO)-n1nc(cc1-c1ccccc1Cl)C(F)(F)F Show InChI InChI=1S/C17H13ClF3N3O3S/c18-13-4-2-1-3-12(13)14-8-16(17(19,20)21)23-24(14)11-5-6-15(28(22,26)27)10(7-11)9-25/h1-8,25H,9H2,(H2,22,26,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	6.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138448 (CHEMBL149781 | N-[2-Sulfamoyl-5-(5-p-tolyl-3-trifl...) Show SMILES CC(=O)NCc1cc(ccc1S(N)(=O)=O)-n1nc(cc1-c1ccc(C)cc1)C(F)(F)F Show InChI InChI=1S/C20H19F3N4O3S/c1-12-3-5-14(6-4-12)17-10-19(20(21,22)23)26-27(17)16-7-8-18(31(24,29)30)15(9-16)11-25-13(2)28/h3-10H,11H2,1-2H3,(H,25,28)(H2,24,29,30)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	6.85E+3	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138451 (4-[5-(3-Fluoro-phenyl)-3-trifluoromethyl-pyrazol-1...) Show SMILES NS(=O)(=O)c1ccc(cc1CO)-n1nc(cc1-c1cccc(F)c1)C(F)(F)F Show InChI InChI=1S/C17H13F4N3O3S/c18-12-3-1-2-10(6-12)14-8-16(17(19,20)21)23-24(14)13-4-5-15(28(22,26)27)11(7-13)9-25/h1-8,25H,9H2,(H2,22,26,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	7.05E+3	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM11639 (4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyraz...) Show SMILES Cc1ccc(cc1)-c1cc(nn1-c1ccc(cc1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C17H14F3N3O2S/c1-11-2-4-12(5-3-11)15-10-16(17(18,19)20)22-23(15)13-6-8-14(9-7-13)26(21,24)25/h2-10H,1H3,(H2,21,24,25)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	1.07E+4	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138453 (2-Hydroxymethyl-4-[5-(2-methoxy-phenyl)-3-trifluor...) Show SMILES COc1ccccc1-c1cc(nn1-c1ccc(c(CO)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C18H16F3N3O4S/c1-28-15-5-3-2-4-13(15)14-9-17(18(19,20)21)23-24(14)12-6-7-16(29(22,26)27)11(8-12)10-25/h2-9,25H,10H2,1H3,(H2,22,26,27)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	2.86E+4	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50452007 (CHEMBL2112872) Show SMILES CCC(=O)OCc1cc(ccc1S(N)(=O)=O)-n1nc(cc1-c1ccc(C)cc1)C(F)(F)F Show InChI InChI=1S/C21H20F3N3O4S/c1-3-20(28)31-12-15-10-16(8-9-18(15)32(25,29)30)27-17(11-19(26-27)21(22,23)24)14-6-4-13(2)5-7-14/h4-11H,3,12H2,1-2H3,(H2,25,29,30)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.46E+4	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50138457 (4-[5-(4-Ethylsulfanyl-phenyl)-3-trifluoromethyl-py...) Show SMILES CCSc1ccc(cc1)-c1cc(nn1-c1ccc(c(CO)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C19H18F3N3O3S2/c1-2-29-15-6-3-12(4-7-15)16-10-18(19(20,21)22)24-25(16)14-5-8-17(30(23,27)28)13(9-14)11-26/h3-10,26H,2,11H2,1H3,(H2,23,27,28)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	5.12E+4	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against human Prostaglandin G/H synthase 2 expressed in sf-9 cells infected with baculovirus				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138441 (2-(hydroxymethyl)-4-(5-(4-(methylthio)phenyl)-3-(t...) Show SMILES CSc1ccc(cc1)-c1cc(nn1-c1ccc(c(CO)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C18H16F3N3O3S2/c1-28-14-5-2-11(3-6-14)15-9-17(18(19,20)21)23-24(15)13-4-7-16(29(22,26)27)12(8-13)10-25/h2-9,25H,10H2,1H3,(H2,22,26,27)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	5.97E+4	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138454 (2-Hydroxymethyl-4-[5-(4-methoxy-phenyl)-3-trifluor...) Show SMILES COc1ccc(cc1)-c1cc(nn1-c1ccc(c(CO)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C18H16F3N3O4S/c1-28-14-5-2-11(3-6-14)15-9-17(18(19,20)21)23-24(15)13-4-7-16(29(22,26)27)12(8-13)10-25/h2-9,25H,10H2,1H3,(H2,22,26,27)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	6.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138455 (CHEMBL344540 | N-{5-[5-(4-Methoxy-phenyl)-3-triflu...) Show SMILES COc1ccc(cc1)-c1cc(nn1-c1ccc(c(CNC(C)=O)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C20H19F3N4O4S/c1-12(28)25-11-14-9-15(5-8-18(14)32(24,29)30)27-17(10-19(26-27)20(21,22)23)13-3-6-16(31-2)7-4-13/h3-10H,11H2,1-2H3,(H,25,28)(H2,24,29,30)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138449 (CHEMBL146465 | N-{5-[5-(4-Chloro-phenyl)-3-trifluo...) Show SMILES CC(=O)NCc1cc(ccc1S(N)(=O)=O)-n1nc(cc1-c1ccc(Cl)cc1)C(F)(F)F Show InChI InChI=1S/C19H16ClF3N4O3S/c1-11(28)25-10-13-8-15(6-7-17(13)31(24,29)30)27-16(9-18(26-27)19(21,22)23)12-2-4-14(20)5-3-12/h2-9H,10H2,1H3,(H,25,28)(H2,24,29,30)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138460 (4-[5-(4-Ethoxy-phenyl)-3-trifluoromethyl-pyrazol-1...) Show SMILES CCOc1ccc(cc1)-c1cc(nn1-c1ccc(c(CO)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C19H18F3N3O4S/c1-2-29-15-6-3-12(4-7-15)16-10-18(19(20,21)22)24-25(16)14-5-8-17(30(23,27)28)13(9-14)11-26/h3-10,26H,2,11H2,1H3,(H2,23,27,28)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.35E+5	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138444 (4-(5-(4-bromophenyl)-3-(trifluoromethyl)-1H-pyrazo...) Show SMILES NS(=O)(=O)c1ccc(cc1CO)-n1nc(cc1-c1ccc(Br)cc1)C(F)(F)F Show InChI InChI=1S/C17H13BrF3N3O3S/c18-12-3-1-10(2-4-12)14-8-16(17(19,20)21)23-24(14)13-5-6-15(28(22,26)27)11(7-13)9-25/h1-8,25H,9H2,(H2,22,26,27)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.30E+5	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138452 (2-Hydroxymethyl-4-(5-p-tolyl-3-trifluoromethyl-pyr...) Show SMILES Cc1ccc(cc1)-c1cc(nn1-c1ccc(c(CO)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C18H16F3N3O3S/c1-11-2-4-12(5-3-11)15-9-17(18(19,20)21)23-24(15)14-6-7-16(28(22,26)27)13(8-14)10-25/h2-9,25H,10H2,1H3,(H2,22,26,27)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	2.78E+5	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138457 (4-[5-(4-Ethylsulfanyl-phenyl)-3-trifluoromethyl-py...) Show SMILES CCSc1ccc(cc1)-c1cc(nn1-c1ccc(c(CO)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C19H18F3N3O3S2/c1-2-29-15-6-3-12(4-7-15)16-10-18(19(20,21)22)24-25(16)14-5-8-17(30(23,27)28)13(9-14)11-26/h3-10,26H,2,11H2,1H3,(H2,23,27,28)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138446 (CHEMBL358122 | {2-Methanesulfonyl-5-[5-(4-methoxy-...) Show SMILES COc1ccc(cc1)-c1cc(nn1-c1ccc(c(CO)c1)S(C)(=O)=O)C(F)(F)F Show InChI InChI=1S/C19H17F3N2O4S/c1-28-15-6-3-12(4-7-15)16-10-18(19(20,21)22)23-24(16)14-5-8-17(29(2,26)27)13(9-14)11-25/h3-10,25H,11H2,1-2H3	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138458 (2-Hydroxymethyl-4-(5-m-tolyl-3-trifluoromethyl-pyr...) Show SMILES Cc1cccc(c1)-c1cc(nn1-c1ccc(c(CO)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C18H16F3N3O3S/c1-11-3-2-4-12(7-11)15-9-17(18(19,20)21)23-24(15)14-5-6-16(28(22,26)27)13(8-14)10-25/h2-9,25H,10H2,1H3,(H2,22,26,27)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.27E+5	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138447 (4-[5-(4-Chloro-phenyl)-3-trifluoromethyl-pyrazol-1...) Show SMILES NS(=O)(=O)c1ccc(cc1CO)-n1nc(cc1-c1ccc(Cl)cc1)C(F)(F)F Show InChI InChI=1S/C17H13ClF3N3O3S/c18-12-3-1-10(2-4-12)14-8-16(17(19,20)21)23-24(14)13-5-6-15(28(22,26)27)11(7-13)9-25/h1-8,25H,9H2,(H2,22,26,27)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.36E+5	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138459 (4-[5-(3-Chloro-phenyl)-3-trifluoromethyl-pyrazol-1...) Show SMILES NS(=O)(=O)c1ccc(cc1CO)-n1nc(cc1-c1cccc(Cl)c1)C(F)(F)F Show InChI InChI=1S/C17H13ClF3N3O3S/c18-12-3-1-2-10(6-12)14-8-16(17(19,20)21)23-24(14)13-4-5-15(28(22,26)27)11(7-13)9-25/h1-8,25H,9H2,(H2,22,26,27)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	4.65E+5	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138442 (4-[5-(4-Fluoro-phenyl)-3-trifluoromethyl-pyrazol-1...) Show SMILES NS(=O)(=O)c1ccc(cc1CO)-n1nc(cc1-c1ccc(F)cc1)C(F)(F)F Show InChI InChI=1S/C17H13F4N3O3S/c18-12-3-1-10(2-4-12)14-8-16(17(19,20)21)23-24(14)13-5-6-15(28(22,26)27)11(7-13)9-25/h1-8,25H,9H2,(H2,22,26,27)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138461 (4-[5-(2-Fluoro-phenyl)-3-trifluoromethyl-pyrazol-1...) Show SMILES NS(=O)(=O)c1ccc(cc1CO)-n1nc(cc1-c1ccccc1F)C(F)(F)F Show InChI InChI=1S/C17H13F4N3O3S/c18-13-4-2-1-3-12(13)14-8-16(17(19,20)21)23-24(14)11-5-6-15(28(22,26)27)10(7-11)9-25/h1-8,25H,9H2,(H2,22,26,27)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138445 (4-[5-(4-Ethyl-phenyl)-3-trifluoromethyl-pyrazol-1-...) Show SMILES CCc1ccc(cc1)-c1cc(nn1-c1ccc(c(CO)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C19H18F3N3O3S/c1-2-12-3-5-13(6-4-12)16-10-18(19(20,21)22)24-25(16)15-7-8-17(29(23,27)28)14(9-15)11-26/h3-10,26H,2,11H2,1H3,(H2,23,27,28)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138443 (4-[5-(2-Chloro-phenyl)-3-trifluoromethyl-pyrazol-1...) Show SMILES NS(=O)(=O)c1ccc(cc1CO)-n1nc(cc1-c1ccccc1Cl)C(F)(F)F Show InChI InChI=1S/C17H13ClF3N3O3S/c18-13-4-2-1-3-12(13)14-8-16(17(19,20)21)23-24(14)11-5-6-15(28(22,26)27)10(7-11)9-25/h1-8,25H,9H2,(H2,22,26,27)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.12E+5	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138451 (4-[5-(3-Fluoro-phenyl)-3-trifluoromethyl-pyrazol-1...) Show SMILES NS(=O)(=O)c1ccc(cc1CO)-n1nc(cc1-c1cccc(F)c1)C(F)(F)F Show InChI InChI=1S/C17H13F4N3O3S/c18-12-3-1-2-10(6-12)14-8-16(17(19,20)21)23-24(14)13-4-5-15(28(22,26)27)11(7-13)9-25/h1-8,25H,9H2,(H2,22,26,27)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138456 (2-Hydroxymethyl-4-(5-phenyl-3-trifluoromethyl-pyra...) Show SMILES NS(=O)(=O)c1ccc(cc1CO)-n1nc(cc1-c1ccccc1)C(F)(F)F Show InChI InChI=1S/C17H14F3N3O3S/c18-17(19,20)16-9-14(11-4-2-1-3-5-11)23(22-16)13-6-7-15(27(21,25)26)12(8-13)10-24/h1-9,24H,10H2,(H2,21,25,26)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.09E+6	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Ovis aries (Sheep))	BDBM50138453 (2-Hydroxymethyl-4-[5-(2-methoxy-phenyl)-3-trifluor...) Show SMILES COc1ccccc1-c1cc(nn1-c1ccc(c(CO)c1)S(N)(=O)=O)C(F)(F)F Show InChI InChI=1S/C18H16F3N3O4S/c1-28-15-5-3-2-4-13(15)14-9-17(18(19,20)21)23-24(14)12-6-7-16(29(22,26)27)11(8-12)10-25/h2-9,25H,10H2,1H3,(H2,22,26,27)	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.15E+6	n/a	n/a	n/a	n/a	n/a	n/a
Discovery Research-Dr. Reddy's Laboratories Ltd Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1 from ram seminal vesicles				Bioorg Med Chem Lett 14: 499-504 (2003) BindingDB Entry DOI: 10.7270/Q280522Q
					More data for this Ligand-Target Pair