Compile Data Set for Download or QSAR

Found 76 hits of ic50 data for polymerid = 50002559   

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
Prostacyclin synthase (Homo sapiens (Human))	BDBM50022222 (2-Imidazol-1-ylmethyl-3-methyl-benzofuran-5-carbox...) Show SMILES Cc1c(Cn2ccnc2)oc2ccc(cc12)C(O)=O Show InChI InChI=1S/C14H12N2O3/c1-9-11-6-10(14(17)18)2-3-12(11)19-13(9)7-16-5-4-15-8-16/h2-6,8H,7H2,1H3,(H,17,18)	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
TBA Curated by ChEMBL					Assay Description Inhibition of porcine aorta prostacyclin PGI-2 synthetase				J Med Chem 29: 1643-50 (1986) BindingDB Entry DOI: 10.7270/Q2C8289W
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036377 ((Z)-6-{2-[1-(4-Fluoro-phenoxy)-1-methyl-ethyl]-4-p...) Show SMILES CC(C)(Oc1ccc(F)cc1)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C24H28FNO5/c1-24(2,31-20-12-10-19(25)11-13-20)23-29-16-18(7-4-3-5-9-21(27)28)22(30-23)17-8-6-14-26-15-17/h3-4,6,8,10-15,18,22-23H,5,7,9,16H2,1-2H3,(H,27,28)/b4-3-	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	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036359 ((Z)-6-{2-[2-(4-Fluoro-phenyl)-1,1-dimethyl-ethyl]-...) Show SMILES CC(C)(Cc1ccc(F)cc1)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C25H30FNO4/c1-25(2,15-18-10-12-21(26)13-11-18)24-30-17-20(7-4-3-5-9-22(28)29)23(31-24)19-8-6-14-27-16-19/h3-4,6,8,10-14,16,20,23-24H,5,7,9,15,17H2,1-2H3,(H,28,29)/b4-3-	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	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036344 ((Z)-6-{2-[1-(2-Methanesulfonyl-phenoxy)-1-methyl-e...) Show SMILES CC(C)(Oc1ccccc1S(C)(=O)=O)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C25H31NO7S/c1-25(2,33-20-12-7-8-13-21(20)34(3,29)30)24-31-17-19(10-5-4-6-14-22(27)28)23(32-24)18-11-9-15-26-16-18/h4-5,7-9,11-13,15-16,19,23-24H,6,10,14,17H2,1-3H3,(H,27,28)/b5-4-	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	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036376 ((Z)-6-[2-(2,4-Dichloro-phenyl)-4-pyridin-3-yl-[1,3...) Show SMILES OC(=O)CC\C=C/CC1COC(OC1c1cccnc1)c1ccc(Cl)cc1Cl Show InChI InChI=1S/C21H21Cl2NO4/c22-16-8-9-17(18(23)11-16)21-27-13-15(5-2-1-3-7-19(25)26)20(28-21)14-6-4-10-24-12-14/h1-2,4,6,8-12,15,20-21H,3,5,7,13H2,(H,25,26)/b2-1-	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	2.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036351 ((Z)-6-{2-[1-(2-Cyano-phenoxy)-1-methyl-ethyl]-4-py...) Show SMILES CC(C)(Oc1ccccc1C#N)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C25H28N2O5/c1-25(2,32-21-12-7-6-9-18(21)15-26)24-30-17-20(10-4-3-5-13-22(28)29)23(31-24)19-11-8-14-27-16-19/h3-4,6-9,11-12,14,16,20,23-24H,5,10,13,17H2,1-2H3,(H,28,29)/b4-3-	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	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036362 ((Z)-6-{2-[1-(4-Bromo-phenoxy)-1-methyl-ethyl]-4-py...) Show SMILES CC(C)(Oc1ccc(Br)cc1)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C24H28BrNO5/c1-24(2,31-20-12-10-19(25)11-13-20)23-29-16-18(7-4-3-5-9-21(27)28)22(30-23)17-8-6-14-26-15-17/h3-4,6,8,10-15,18,22-23H,5,7,9,16H2,1-2H3,(H,27,28)/b4-3-	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	4.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036370 ((Z)-6-{2-[1-(4-Cyano-phenoxy)-1-methyl-ethyl]-4-py...) Show SMILES CC(C)(Oc1ccc(cc1)C#N)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C25H28N2O5/c1-25(2,32-21-12-10-18(15-26)11-13-21)24-30-17-20(7-4-3-5-9-22(28)29)23(31-24)19-8-6-14-27-16-19/h3-4,6,8,10-14,16,20,23-24H,5,7,9,17H2,1-2H3,(H,28,29)/b4-3-	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	4.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036362 ((Z)-6-{2-[1-(4-Bromo-phenoxy)-1-methyl-ethyl]-4-py...) Show SMILES CC(C)(Oc1ccc(Br)cc1)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C24H28BrNO5/c1-24(2,31-20-12-10-19(25)11-13-20)23-29-16-18(7-4-3-5-9-21(27)28)22(30-23)17-8-6-14-26-15-17/h3-4,6,8,10-15,18,22-23H,5,7,9,16H2,1-2H3,(H,27,28)/b4-3-	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	4.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036387 ((Z)-6-{2-[1-(4-Acetyl-2-nitro-phenoxy)-1-methyl-et...) Show SMILES CC(=O)c1ccc(OC(C)(C)C2OCC(C\C=C/CCC(O)=O)C(O2)c2cccnc2)c(c1)[N+]([O-])=O Show InChI InChI=1S/C26H30N2O8/c1-17(29)18-11-12-22(21(14-18)28(32)33)36-26(2,3)25-34-16-20(8-5-4-6-10-23(30)31)24(35-25)19-9-7-13-27-15-19/h4-5,7,9,11-15,20,24-25H,6,8,10,16H2,1-3H3,(H,30,31)/b5-4-	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	4.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036345 ((Z)-6-{2-[1-Methyl-1-(4-methylsulfanyl-2-nitro-phe...) Show SMILES CSc1ccc(OC(C)(C)C2OCC(C\C=C/CCC(O)=O)C(O2)c2cccnc2)c(c1)[N+]([O-])=O Show InChI InChI=1S/C25H30N2O7S/c1-25(2,34-21-12-11-19(35-3)14-20(21)27(30)31)24-32-16-18(8-5-4-6-10-22(28)29)23(33-24)17-9-7-13-26-15-17/h4-5,7,9,11-15,18,23-24H,6,8,10,16H2,1-3H3,(H,28,29)/b5-4-	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	5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036356 ((Z)-6-{2-[2-(2-Cyano-4-fluoro-phenyl)-1,1-dimethyl...) Show SMILES CC(C)(Cc1ccc(F)cc1C#N)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C26H29FN2O4/c1-26(2,14-18-10-11-22(27)13-21(18)15-28)25-32-17-20(7-4-3-5-9-23(30)31)24(33-25)19-8-6-12-29-16-19/h3-4,6,8,10-13,16,20,24-25H,5,7,9,14,17H2,1-2H3,(H,30,31)/b4-3-	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	7.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036372 ((Z)-6-{2-[1-(2-Bromo-phenoxy)-1-methyl-ethyl]-4-py...) Show SMILES CC(C)(Oc1ccccc1Br)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C24H28BrNO5/c1-24(2,31-20-12-7-6-11-19(20)25)23-29-16-18(9-4-3-5-13-21(27)28)22(30-23)17-10-8-14-26-15-17/h3-4,6-8,10-12,14-15,18,22-23H,5,9,13,16H2,1-2H3,(H,27,28)/b4-3-	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	7.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036386 ((Z)-6-{2-[1-(4-Methanesulfonyl-phenoxy)-1-methyl-e...) Show SMILES CC(C)(Oc1ccc(cc1)S(C)(=O)=O)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C25H31NO7S/c1-25(2,33-20-11-13-21(14-12-20)34(3,29)30)24-31-17-19(8-5-4-6-10-22(27)28)23(32-24)18-9-7-15-26-16-18/h4-5,7,9,11-16,19,23-24H,6,8,10,17H2,1-3H3,(H,27,28)/b5-4-	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	8.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036354 ((Z)-6-{2-[1-(4-Fluoro-2-nitro-phenoxy)-1-methyl-et...) Show SMILES CC(C)(Oc1ccc(F)cc1[N+]([O-])=O)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C24H27FN2O7/c1-24(2,34-20-11-10-18(25)13-19(20)27(30)31)23-32-15-17(7-4-3-5-9-21(28)29)22(33-23)16-8-6-12-26-14-16/h3-4,6,8,10-14,17,22-23H,5,7,9,15H2,1-2H3,(H,28,29)/b4-3-	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	9.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036363 ((Z)-6-[2-(3,4-Dichloro-phenyl)-4-pyridin-3-yl-[1,3...) Show SMILES OC(=O)CC\C=C/CC1COC(OC1c1cccnc1)c1ccc(Cl)c(Cl)c1 Show InChI InChI=1S/C21H21Cl2NO4/c22-17-9-8-14(11-18(17)23)21-27-13-16(5-2-1-3-7-19(25)26)20(28-21)15-6-4-10-24-12-15/h1-2,4,6,8-12,16,20-21H,3,5,7,13H2,(H,25,26)/b2-1-	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	9.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036361 ((Z)-6-{2-[1-(2-Cyano-4-methyl-phenoxy)-1-methyl-et...) Show SMILES Cc1ccc(OC(C)(C)C2OCC(C\C=C/CCC(O)=O)C(O2)c2cccnc2)c(c1)C#N Show InChI InChI=1S/C26H30N2O5/c1-18-11-12-22(21(14-18)15-27)33-26(2,3)25-31-17-20(8-5-4-6-10-23(29)30)24(32-25)19-9-7-13-28-16-19/h4-5,7,9,11-14,16,20,24-25H,6,8,10,17H2,1-3H3,(H,29,30)/b5-4-	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	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036361 ((Z)-6-{2-[1-(2-Cyano-4-methyl-phenoxy)-1-methyl-et...) Show SMILES Cc1ccc(OC(C)(C)C2OCC(C\C=C/CCC(O)=O)C(O2)c2cccnc2)c(c1)C#N Show InChI InChI=1S/C26H30N2O5/c1-18-11-12-22(21(14-18)15-27)33-26(2,3)25-31-17-20(8-5-4-6-10-23(29)30)24(32-25)19-9-7-13-28-16-19/h4-5,7,9,11-14,16,20,24-25H,6,8,10,17H2,1-3H3,(H,29,30)/b5-4-	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	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036368 ((Z)-6-[2-(1,1-Dimethyl-2-phenyl-ethyl)-4-pyridin-3...) Show SMILES CC(C)(Cc1ccccc1)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C25H31NO4/c1-25(2,16-19-10-5-3-6-11-19)24-29-18-21(12-7-4-8-14-22(27)28)23(30-24)20-13-9-15-26-17-20/h3-7,9-11,13,15,17,21,23-24H,8,12,14,16,18H2,1-2H3,(H,27,28)/b7-4-	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	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036374 ((Z)-6-[2-(4-Nitro-phenyl)-4-pyridin-3-yl-[1,3]diox...) Show SMILES OC(=O)CC\C=C/CC1COC(OC1c1cccnc1)c1ccc(cc1)[N+]([O-])=O Show InChI InChI=1S/C21H22N2O6/c24-19(25)7-3-1-2-5-17-14-28-21(15-8-10-18(11-9-15)23(26)27)29-20(17)16-6-4-12-22-13-16/h1-2,4,6,8-13,17,20-21H,3,5,7,14H2,(H,24,25)/b2-1-	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	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036380 ((Z)-6-{2-[2-(2-Cyano-phenyl)-1,1-dimethyl-ethyl]-4...) Show SMILES CC(C)(Cc1ccccc1C#N)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C26H30N2O4/c1-26(2,15-19-9-6-7-10-20(19)16-27)25-31-18-22(11-4-3-5-13-23(29)30)24(32-25)21-12-8-14-28-17-21/h3-4,6-10,12,14,17,22,24-25H,5,11,13,15,18H2,1-2H3,(H,29,30)/b4-3-	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	1.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036346 ((Z)-6-{2-[1-(4-Methoxy-2-nitro-phenoxy)-1-methyl-e...) Show SMILES COc1ccc(OC(C)(C)C2OCC(C\C=C/CCC(O)=O)C(O2)c2cccnc2)c(c1)[N+]([O-])=O Show InChI InChI=1S/C25H30N2O8/c1-25(2,35-21-12-11-19(32-3)14-20(21)27(30)31)24-33-16-18(8-5-4-6-10-22(28)29)23(34-24)17-9-7-13-26-15-17/h4-5,7,9,11-15,18,23-24H,6,8,10,16H2,1-3H3,(H,28,29)/b5-4-	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	2.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036382 ((Z)-6-[2-(1-Methyl-1-p-tolyloxy-ethyl)-4-pyridin-3...) Show SMILES Cc1ccc(OC(C)(C)C2OCC(C\C=C/CCC(O)=O)C(O2)c2cccnc2)cc1 Show InChI InChI=1S/C25H31NO5/c1-18-11-13-21(14-12-18)31-25(2,3)24-29-17-20(8-5-4-6-10-22(27)28)23(30-24)19-9-7-15-26-16-19/h4-5,7,9,11-16,20,23-24H,6,8,10,17H2,1-3H3,(H,27,28)/b5-4-	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	2.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036360 ((Z)-6-{2-[1-Methyl-1-(4-methylsulfanyl-phenoxy)-et...) Show SMILES CSc1ccc(OC(C)(C)C2OCC(C\C=C/CCC(O)=O)C(O2)c2cccnc2)cc1 Show InChI InChI=1S/C25H31NO5S/c1-25(2,31-20-11-13-21(32-3)14-12-20)24-29-17-19(8-5-4-6-10-22(27)28)23(30-24)18-9-7-15-26-16-18/h4-5,7,9,11-16,19,23-24H,6,8,10,17H2,1-3H3,(H,27,28)/b5-4-	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	3.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036365 ((Z)-6-{2-[1-Methyl-1-(4-methyl-2-nitro-phenoxy)-et...) Show SMILES Cc1ccc(OC(C)(C)C2OCC(C\C=C/CCC(O)=O)C(O2)c2cccnc2)c(c1)[N+]([O-])=O Show InChI InChI=1S/C25H30N2O7/c1-17-11-12-21(20(14-17)27(30)31)34-25(2,3)24-32-16-19(8-5-4-6-10-22(28)29)23(33-24)18-9-7-13-26-15-18/h4-5,7,9,11-15,19,23-24H,6,8,10,16H2,1-3H3,(H,28,29)/b5-4-	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	3.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036365 ((Z)-6-{2-[1-Methyl-1-(4-methyl-2-nitro-phenoxy)-et...) Show SMILES Cc1ccc(OC(C)(C)C2OCC(C\C=C/CCC(O)=O)C(O2)c2cccnc2)c(c1)[N+]([O-])=O Show InChI InChI=1S/C25H30N2O7/c1-17-11-12-21(20(14-17)27(30)31)34-25(2,3)24-32-16-19(8-5-4-6-10-22(28)29)23(33-24)18-9-7-13-26-15-18/h4-5,7,9,11-15,19,23-24H,6,8,10,16H2,1-3H3,(H,28,29)/b5-4-	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	3.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036355 ((Z)-6-{2-[1-(2-Cyano-4-fluoro-phenoxy)-1-methyl-et...) Show SMILES CC(C)(Oc1ccc(F)cc1C#N)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C25H27FN2O5/c1-25(2,33-21-11-10-20(26)13-19(21)14-27)24-31-16-18(7-4-3-5-9-22(29)30)23(32-24)17-8-6-12-28-15-17/h3-4,6,8,10-13,15,18,23-24H,5,7,9,16H2,1-2H3,(H,29,30)/b4-3-	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	3.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036349 ((Z)-6-{2-[1-(3-Fluoro-phenoxy)-1-methyl-ethyl]-4-p...) Show SMILES CC(C)(Oc1cccc(F)c1)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C24H28FNO5/c1-24(2,31-20-11-6-10-19(25)14-20)23-29-16-18(8-4-3-5-12-21(27)28)22(30-23)17-9-7-13-26-15-17/h3-4,6-7,9-11,13-15,18,22-23H,5,8,12,16H2,1-2H3,(H,27,28)/b4-3-	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	4.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036369 ((Z)-6-{2-[1-(2-Methoxy-phenoxy)-1-methyl-ethyl]-4-...) Show SMILES COc1ccccc1OC(C)(C)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C25H31NO6/c1-25(2,32-21-13-8-7-12-20(21)29-3)24-30-17-19(10-5-4-6-14-22(27)28)23(31-24)18-11-9-15-26-16-18/h4-5,7-9,11-13,15-16,19,23-24H,6,10,14,17H2,1-3H3,(H,27,28)/b5-4-	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	5.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036373 ((Z)-6-{2-[1-(2-Cyano-6-methyl-phenoxy)-1-methyl-et...) Show SMILES Cc1cccc(C#N)c1OC(C)(C)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C26H30N2O5/c1-18-9-7-11-19(15-27)23(18)33-26(2,3)25-31-17-21(10-5-4-6-13-22(29)30)24(32-25)20-12-8-14-28-16-20/h4-5,7-9,11-12,14,16,21,24-25H,6,10,13,17H2,1-3H3,(H,29,30)/b5-4-	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	6.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036350 (2-{1-[5-((Z)-5-Carboxy-pent-2-enyl)-4-pyridin-3-yl...) Show SMILES COC(=O)c1ccccc1OC(C)(C)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C26H31NO7/c1-26(2,34-21-13-8-7-12-20(21)24(30)31-3)25-32-17-19(10-5-4-6-14-22(28)29)23(33-25)18-11-9-15-27-16-18/h4-5,7-9,11-13,15-16,19,23,25H,6,10,14,17H2,1-3H3,(H,28,29)/b5-4-	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	7.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50036371 ((Z)-6-[2-(1-Methyl-1-phenoxy-ethyl)-4-pyridin-3-yl...) Show SMILES CC(C)(Oc1ccccc1)C1OCC(C\C=C/CCC(O)=O)C(O1)c1cccnc1 Show InChI InChI=1S/C24H29NO5/c1-24(2,30-20-12-6-4-7-13-20)23-28-17-19(10-5-3-8-14-21(26)27)22(29-23)18-11-9-15-25-16-18/h3-7,9,11-13,15-16,19,22-23H,8,10,14,17H2,1-2H3,(H,26,27)/b5-3-	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	7.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
ZENECA Pharmaceuticals Curated by ChEMBL					Assay Description In vitro inhibition of Prostaglandin I2 synthase from human blood platelet microsomes				J Med Chem 38: 686-94 (1995) BindingDB Entry DOI: 10.7270/Q24Q7T2K
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM7962 (4-(2-Imidazol-1-yl-ethoxy)-benzoic acid; hydrochlo...) Show SMILES OC(=O)c1ccc(OCCn2ccnc2)cc1 Show InChI InChI=1S/C12H12N2O3/c15-12(16)10-1-3-11(4-2-10)17-8-7-14-6-5-13-9-14/h1-6,9H,7-8H2,(H,15,16)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of PGI-2 synthetase from porcine aorta				J Med Chem 29: 342-6 (1986) BindingDB Entry DOI: 10.7270/Q2W66JSZ
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50022119 (3-(5-Chloro-3-imidazol-1-ylmethyl-indol-1-yl)-prop...) Show SMILES OC(=O)CCn1cc(Cn2ccnc2)c2cc(Cl)ccc12 Show InChI InChI=1S/C15H14ClN3O2/c16-12-1-2-14-13(7-12)11(8-18-6-4-17-10-18)9-19(14)5-3-15(20)21/h1-2,4,6-7,9-10H,3,5,8H2,(H,20,21)	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	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of PGI-2 synthetase from porcine aorta				J Med Chem 29: 342-6 (1986) BindingDB Entry DOI: 10.7270/Q2W66JSZ
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50022122 (3-(3-Imidazol-1-ylmethyl-5-methoxy-indol-1-yl)-pro...) Show SMILES COc1ccc2n(CCC(O)=O)cc(Cn3ccnc3)c2c1 Show InChI InChI=1S/C16H17N3O3/c1-22-13-2-3-15-14(8-13)12(9-18-7-5-17-11-18)10-19(15)6-4-16(20)21/h2-3,5,7-8,10-11H,4,6,9H2,1H3,(H,20,21)	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	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of PGI-2 synthetase from porcine aorta				J Med Chem 29: 342-6 (1986) BindingDB Entry DOI: 10.7270/Q2W66JSZ
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50000317 (3-(3-Imidazol-1-ylmethyl-2-methyl-indol-1-yl)-prop...) Show SMILES Cc1c(Cn2ccnc2)c2ccccc2n1CCC(O)=O Show InChI InChI=1S/C16H17N3O2/c1-12-14(10-18-9-7-17-11-18)13-4-2-3-5-15(13)19(12)8-6-16(20)21/h2-5,7,9,11H,6,8,10H2,1H3,(H,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of PGI-2 synthetase from porcine aorta				J Med Chem 29: 342-6 (1986) BindingDB Entry DOI: 10.7270/Q2W66JSZ
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50022124 (3-(3-Imidazol-1-ylmethyl-indol-1-yl)-propionic aci...) Show SMILES OC(=O)CCn1cc(Cn2ccnc2)c2ccccc12 Show InChI InChI=1S/C15H15N3O2/c19-15(20)5-7-18-10-12(9-17-8-6-16-11-17)13-3-1-2-4-14(13)18/h1-4,6,8,10-11H,5,7,9H2,(H,19,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of PGI-2 synthetase from porcine aorta				J Med Chem 29: 342-6 (1986) BindingDB Entry DOI: 10.7270/Q2W66JSZ
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50022126 ((3-Imidazol-1-ylmethyl-indol-1-yl)-acetic acid | C...) Show SMILES OC(=O)Cn1cc(Cn2ccnc2)c2ccccc12 Show InChI InChI=1S/C14H13N3O2/c18-14(19)9-17-8-11(7-16-6-5-15-10-16)12-3-1-2-4-13(12)17/h1-6,8,10H,7,9H2,(H,18,19)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of PGI-2 synthetase from porcine aorta				J Med Chem 29: 342-6 (1986) BindingDB Entry DOI: 10.7270/Q2W66JSZ
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50022121 (3-Imidazol-1-ylmethyl-2-isopropyl-1H-indole | 3-Im...) Show SMILES CC(C)c1[nH]c2ccccc2c1Cn1ccnc1 Show InChI InChI=1S/C15H17N3/c1-11(2)15-13(9-18-8-7-16-10-18)12-5-3-4-6-14(12)17-15/h3-8,10-11,17H,9H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of PGI-2 synthetase from porcine aorta				J Med Chem 29: 342-6 (1986) BindingDB Entry DOI: 10.7270/Q2W66JSZ
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50022125 (3-(5-Dimethylamino-3-imidazol-1-ylmethyl-indol-1-y...) Show SMILES CN(C)c1ccc2n(CCC(O)=O)cc(Cn3ccnc3)c2c1 Show InChI InChI=1S/C17H20N4O2/c1-19(2)14-3-4-16-15(9-14)13(10-20-8-6-18-12-20)11-21(16)7-5-17(22)23/h3-4,6,8-9,11-12H,5,7,10H2,1-2H3,(H,22,23)	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	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of PGI-2 synthetase from porcine aorta				J Med Chem 29: 342-6 (1986) BindingDB Entry DOI: 10.7270/Q2W66JSZ
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50022131 (3-(3-Imidazol-1-ylmethyl-6-trifluoromethyl-indol-1...) Show SMILES OC(=O)CCn1cc(Cn2ccnc2)c2ccc(cc12)C(F)(F)F Show InChI InChI=1S/C16H14F3N3O2/c17-16(18,19)12-1-2-13-11(8-21-6-4-20-10-21)9-22(14(13)7-12)5-3-15(23)24/h1-2,4,6-7,9-10H,3,5,8H2,(H,23,24)	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	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of PGI-2 synthetase from porcine aorta				J Med Chem 29: 342-6 (1986) BindingDB Entry DOI: 10.7270/Q2W66JSZ
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50022127 (3-(3-Imidazol-1-ylmethyl-5-methyl-indol-1-yl)-prop...) Show SMILES Cc1ccc2n(CCC(O)=O)cc(Cn3ccnc3)c2c1 Show InChI InChI=1S/C16H17N3O2/c1-12-2-3-15-14(8-12)13(9-18-7-5-17-11-18)10-19(15)6-4-16(20)21/h2-3,5,7-8,10-11H,4,6,9H2,1H3,(H,20,21)	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	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of PGI-2 synthetase from porcine aorta				J Med Chem 29: 342-6 (1986) BindingDB Entry DOI: 10.7270/Q2W66JSZ
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50022118 (3-(3-Imidazol-1-ylmethyl-2-isopropyl-indol-1-yl)-p...) Show SMILES CC(C)c1c(Cn2ccnc2)c2ccccc2n1CCC(O)=O Show InChI InChI=1S/C18H21N3O2/c1-13(2)18-15(11-20-10-8-19-12-20)14-5-3-4-6-16(14)21(18)9-7-17(22)23/h3-6,8,10,12-13H,7,9,11H2,1-2H3,(H,22,23)	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	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of PGI-2 synthetase from porcine aorta				J Med Chem 29: 342-6 (1986) BindingDB Entry DOI: 10.7270/Q2W66JSZ
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50022130 (3-(2-Cyclopropyl-3-imidazol-1-ylmethyl-indol-1-yl)...) Show SMILES OC(=O)CCn1c(C2CC2)c(Cn2ccnc2)c2ccccc12 Show InChI InChI=1S/C18H19N3O2/c22-17(23)7-9-21-16-4-2-1-3-14(16)15(18(21)13-5-6-13)11-20-10-8-19-12-20/h1-4,8,10,12-13H,5-7,9,11H2,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of PGI-2 synthetase from porcine aorta				J Med Chem 29: 342-6 (1986) BindingDB Entry DOI: 10.7270/Q2W66JSZ
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50022129 (3-(5-Bromo-3-imidazol-1-ylmethyl-indol-1-yl)-propi...) Show SMILES OC(=O)CCn1cc(Cn2ccnc2)c2cc(Br)ccc12 Show InChI InChI=1S/C15H14BrN3O2/c16-12-1-2-14-13(7-12)11(8-18-6-4-17-10-18)9-19(14)5-3-15(20)21/h1-2,4,6-7,9-10H,3,5,8H2,(H,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of PGI-2 synthetase from porcine aorta				J Med Chem 29: 342-6 (1986) BindingDB Entry DOI: 10.7270/Q2W66JSZ
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50022123 (3-(3-Imidazol-1-ylmethyl-2-methyl-indol-1-yl)-acry...) Show SMILES Cc1c(Cn2ccnc2)c2ccccc2n1\C=C\C(O)=O Show InChI InChI=1S/C16H15N3O2/c1-12-14(10-18-9-7-17-11-18)13-4-2-3-5-15(13)19(12)8-6-16(20)21/h2-9,11H,10H2,1H3,(H,20,21)/b8-6+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of PGI-2 synthetase from porcine aorta				J Med Chem 29: 342-6 (1986) BindingDB Entry DOI: 10.7270/Q2W66JSZ
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50022223 (3-Chloro-2-imidazol-1-ylmethyl-benzofuran-5-carbox...) Show SMILES OC(=O)c1ccc2oc(Cn3ccnc3)c(Cl)c2c1 Show InChI InChI=1S/C13H9ClN2O3/c14-12-9-5-8(13(17)18)1-2-10(9)19-11(12)6-16-4-3-15-7-16/h1-5,7H,6H2,(H,17,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of porcine aorta prostacyclin PGI-2 synthetase				J Med Chem 29: 1643-50 (1986) BindingDB Entry DOI: 10.7270/Q2C8289W
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50022219 (2-Imidazol-1-ylmethyl-3-methyl-benzo[b]thiophene-6...) Show SMILES Cc1c(Cn2ccnc2)sc2cc(ccc12)C(O)=O Show InChI InChI=1S/C14H12N2O2S/c1-9-11-3-2-10(14(17)18)6-12(11)19-13(9)7-16-5-4-15-8-16/h2-6,8H,7H2,1H3,(H,17,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of porcine aorta prostacyclin PGI-2 synthetase				J Med Chem 29: 1643-50 (1986) BindingDB Entry DOI: 10.7270/Q2C8289W
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50022217 (2-Imidazol-1-ylmethyl-benzo[b]thiophene-5-carboxyl...) Show SMILES OC(=O)c1ccc2sc(Cn3ccnc3)cc2c1 Show InChI InChI=1S/C13H10N2O2S/c16-13(17)9-1-2-12-10(5-9)6-11(18-12)7-15-4-3-14-8-15/h1-6,8H,7H2,(H,16,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase 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
TBA Curated by ChEMBL					Assay Description Inhibition of porcine aorta prostacyclin PGI-2 synthetase				J Med Chem 29: 1643-50 (1986) BindingDB Entry DOI: 10.7270/Q2C8289W
					More data for this Ligand-Target Pair
Prostacyclin synthase (Homo sapiens (Human))	BDBM50022227 (3-Chloro-2-imidazol-1-ylmethyl-benzo[b]thiophene-6...) Show SMILES OC(=O)c1ccc2c(Cl)c(Cn3ccnc3)sc2c1 Show InChI InChI=1S/C13H9ClN2O2S/c14-12-9-2-1-8(13(17)18)5-10(9)19-11(12)6-16-4-3-15-7-16/h1-5,7H,6H2,(H,17,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of porcine aorta prostacyclin PGI-2 synthetase				J Med Chem 29: 1643-50 (1986) BindingDB Entry DOI: 10.7270/Q2C8289W
					More data for this Ligand-Target Pair

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