Compile Data Set for Download or QSAR

Found 135 hits Enz. Inhib. hit(s) with all data for entry = 50033363   

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))	BDBM50056999 (CHEMBL56367 | nimesulide) Show SMILES CS(=O)(=O)Nc1ccc(cc1Oc1ccccc1)[N+]([O-])=O Show InChI InChI=1S/C13H12N2O5S/c1-21(18,19)14-12-8-7-10(15(16)17)9-13(12)20-11-5-3-2-4-6-11/h2-9,14H,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	DrugBank Article PubMed	n/a	n/a	23	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of purified COX2 assessed as formation of oxidized TMPD during reduction og PGG2 to PGH2 preincubated for 15 mins by chromogenic assay				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343920 (4-(4-(2-(Pyrrolidin-1-yl)ethoxy)phenoxy)aniline | ...) Show SMILES Nc1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C18H22N2O2/c19-15-3-5-17(6-4-15)22-18-9-7-16(8-10-18)21-14-13-20-11-1-2-12-20/h3-10H,1-2,11-14,19H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	29	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50085245 (1-[2-(4-Phenoxy-phenoxy)-ethyl]-pyrrolidine | CHEM...) Show SMILES C(CN1CCCC1)Oc1ccc(Oc2ccccc2)cc1 Show InChI InChI=1S/C18H21NO2/c1-2-6-17(7-3-1)21-18-10-8-16(9-11-18)20-15-14-19-12-4-5-13-19/h1-3,6-11H,4-5,12-15H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	30	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343916 (1-(2-(4-(4-Chlorophenoxy)phenoxy)ethyl)pyrrolidine...) Show SMILES Clc1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C18H20ClNO2/c19-15-3-5-17(6-4-15)22-18-9-7-16(8-10-18)21-14-13-20-11-1-2-12-20/h3-10H,1-2,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	40	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343915 (1-(2-(4-(4-Fluorophenoxy)phenoxy)ethyl)pyrrolidine...) Show SMILES Fc1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C18H20FNO2/c19-15-3-5-17(6-4-15)22-18-9-7-16(8-10-18)21-14-13-20-11-1-2-12-20/h3-10H,1-2,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	80	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343918 (2-(4-(2-(Pyrrolidin-1-yl)ethoxy)phenoxy)aniline | ...) Show SMILES Nc1ccccc1Oc1ccc(OCCN2CCCC2)cc1 Show InChI InChI=1S/C18H22N2O2/c19-17-5-1-2-6-18(17)22-16-9-7-15(8-10-16)21-14-13-20-11-3-4-12-20/h1-2,5-10H,3-4,11-14,19H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	110	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343917 (1-(2-(4-(4-Bromophenoxy)phenoxy)ethyl)pyrrolidine ...) Show SMILES Brc1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C18H20BrNO2/c19-15-3-5-17(6-4-15)22-18-9-7-16(8-10-18)21-14-13-20-11-1-2-12-20/h3-10H,1-2,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	110	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343904 (2-(4-(2-(Pyrrolidin-1-yl)ethoxy)phenoxy)pyridine |...) Show SMILES C(CN1CCCC1)Oc1ccc(Oc2ccccn2)cc1 Show InChI InChI=1S/C17H20N2O2/c1-2-10-18-17(5-1)21-16-8-6-15(7-9-16)20-14-13-19-11-3-4-12-19/h1-2,5-10H,3-4,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	180	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343912 (1-(2-(4-(2-(Trifluoromethyl)phenoxy)phenoxy)ethyl)...) Show SMILES FC(F)(F)c1ccccc1Oc1ccc(OCCN2CCCC2)cc1 Show InChI InChI=1S/C19H20F3NO2/c20-19(21,22)17-5-1-2-6-18(17)25-16-9-7-15(8-10-16)24-14-13-23-11-3-4-12-23/h1-2,5-10H,3-4,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	220	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343917 (1-(2-(4-(4-Bromophenoxy)phenoxy)ethyl)pyrrolidine ...) Show SMILES Brc1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C18H20BrNO2/c19-15-3-5-17(6-4-15)22-18-9-7-16(8-10-18)21-14-13-20-11-1-2-12-20/h3-10H,1-2,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	290	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343920 (4-(4-(2-(Pyrrolidin-1-yl)ethoxy)phenoxy)aniline | ...) Show SMILES Nc1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C18H22N2O2/c19-15-3-5-17(6-4-15)22-18-9-7-16(8-10-18)21-14-13-20-11-1-2-12-20/h3-10H,1-2,11-14,19H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	320	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343927 (1-(2-(4-(4-Nitrophenoxy)phenoxy)ethyl)pyrrolidine ...) Show SMILES [O-][N+](=O)c1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C18H20N2O4/c21-20(22)15-3-5-17(6-4-15)24-18-9-7-16(8-10-18)23-14-13-19-11-1-2-12-19/h3-10H,1-2,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	370	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343914 (1-(2-(4-(4-(Trifluoromethyl)phenoxy)phenoxy)ethyl)...) Show SMILES FC(F)(F)c1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C19H20F3NO2/c20-19(21,22)15-3-5-17(6-4-15)25-18-9-7-16(8-10-18)24-14-13-23-11-1-2-12-23/h3-10H,1-2,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	390	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343926 (1-(2-(4-(3-Nitrophenoxy)phenoxy)ethyl)pyrrolidine ...) Show SMILES [O-][N+](=O)c1cccc(Oc2ccc(OCCN3CCCC3)cc2)c1 Show InChI InChI=1S/C18H20N2O4/c21-20(22)15-4-3-5-18(14-15)24-17-8-6-16(7-9-17)23-13-12-19-10-1-2-11-19/h3-9,14H,1-2,10-13H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	470	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343913 (1-(2-(4-(3-(Trifluoromethyl)phenoxy)phenoxy)ethyl)...) Show SMILES FC(F)(F)c1cccc(Oc2ccc(OCCN3CCCC3)cc2)c1 Show InChI InChI=1S/C19H20F3NO2/c20-19(21,22)15-4-3-5-18(14-15)25-17-8-6-16(7-9-17)24-13-12-23-10-1-2-11-23/h3-9,14H,1-2,10-13H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	540	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343905 (4-(4-(2-(Pyrrolidin-1-yl)ethoxy)phenoxy)pyridine |...) Show SMILES C(CN1CCCC1)Oc1ccc(Oc2ccncc2)cc1 Show InChI InChI=1S/C17H20N2O2/c1-2-12-19(11-1)13-14-20-15-3-5-16(6-4-15)21-17-7-9-18-10-8-17/h3-10H,1-2,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	580	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343918 (2-(4-(2-(Pyrrolidin-1-yl)ethoxy)phenoxy)aniline | ...) Show SMILES Nc1ccccc1Oc1ccc(OCCN2CCCC2)cc1 Show InChI InChI=1S/C18H22N2O2/c19-17-5-1-2-6-18(17)22-16-9-7-15(8-10-16)21-14-13-20-11-3-4-12-20/h1-2,5-10H,3-4,11-14,19H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	630	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343905 (4-(4-(2-(Pyrrolidin-1-yl)ethoxy)phenoxy)pyridine |...) Show SMILES C(CN1CCCC1)Oc1ccc(Oc2ccncc2)cc1 Show InChI InChI=1S/C17H20N2O2/c1-2-12-19(11-1)13-14-20-15-3-5-16(6-4-15)21-17-7-9-18-10-8-17/h3-10H,1-2,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	670	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343925 (1-(2-(4-(2-Nitrophenoxy)-phenoxy)ethyl)pyrrolidine...) Show SMILES [O-][N+](=O)c1ccccc1Oc1ccc(OCCN2CCCC2)cc1 Show InChI InChI=1S/C18H20N2O4/c21-20(22)17-5-1-2-6-18(17)24-16-9-7-15(8-10-16)23-14-13-19-11-3-4-12-19/h1-2,5-10H,3-4,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	680	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343919 (3-(4-(2-(Pyrrolidin-1-yl)ethoxy)phenoxy)aniline | ...) Show SMILES Nc1cccc(Oc2ccc(OCCN3CCCC3)cc2)c1 Show InChI InChI=1S/C18H22N2O2/c19-15-4-3-5-18(14-15)22-17-8-6-16(7-9-17)21-13-12-20-10-1-2-11-20/h3-9,14H,1-2,10-13,19H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	690	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343927 (1-(2-(4-(4-Nitrophenoxy)phenoxy)ethyl)pyrrolidine ...) Show SMILES [O-][N+](=O)c1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C18H20N2O4/c21-20(22)15-3-5-17(6-4-15)24-18-9-7-16(8-10-18)23-14-13-19-11-1-2-12-19/h3-10H,1-2,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	690	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343916 (1-(2-(4-(4-Chlorophenoxy)phenoxy)ethyl)pyrrolidine...) Show SMILES Clc1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C18H20ClNO2/c19-15-3-5-17(6-4-15)22-18-9-7-16(8-10-18)21-14-13-20-11-1-2-12-20/h3-10H,1-2,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	730	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343912 (1-(2-(4-(2-(Trifluoromethyl)phenoxy)phenoxy)ethyl)...) Show SMILES FC(F)(F)c1ccccc1Oc1ccc(OCCN2CCCC2)cc1 Show InChI InChI=1S/C19H20F3NO2/c20-19(21,22)17-5-1-2-6-18(17)25-16-9-7-15(8-10-16)24-14-13-23-11-3-4-12-23/h1-2,5-10H,3-4,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	730	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343904 (2-(4-(2-(Pyrrolidin-1-yl)ethoxy)phenoxy)pyridine |...) Show SMILES C(CN1CCCC1)Oc1ccc(Oc2ccccn2)cc1 Show InChI InChI=1S/C17H20N2O2/c1-2-10-18-17(5-1)21-16-8-6-15(7-9-16)20-14-13-19-11-3-4-12-19/h1-2,5-10H,3-4,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	770	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50085245 (1-[2-(4-Phenoxy-phenoxy)-ethyl]-pyrrolidine | CHEM...) Show SMILES C(CN1CCCC1)Oc1ccc(Oc2ccccc2)cc1 Show InChI InChI=1S/C18H21NO2/c1-2-6-17(7-3-1)21-18-10-8-16(9-11-18)20-15-14-19-12-4-5-13-19/h1-3,6-11H,4-5,12-15H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	780	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343919 (3-(4-(2-(Pyrrolidin-1-yl)ethoxy)phenoxy)aniline | ...) Show SMILES Nc1cccc(Oc2ccc(OCCN3CCCC3)cc2)c1 Show InChI InChI=1S/C18H22N2O2/c19-15-4-3-5-18(14-15)22-17-8-6-16(7-9-17)21-13-12-20-10-1-2-11-20/h3-9,14H,1-2,10-13,19H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	970	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343915 (1-(2-(4-(4-Fluorophenoxy)phenoxy)ethyl)pyrrolidine...) Show SMILES Fc1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C18H20FNO2/c19-15-3-5-17(6-4-15)22-18-9-7-16(8-10-18)21-14-13-20-11-1-2-12-20/h3-10H,1-2,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	990	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343926 (1-(2-(4-(3-Nitrophenoxy)phenoxy)ethyl)pyrrolidine ...) Show SMILES [O-][N+](=O)c1cccc(Oc2ccc(OCCN3CCCC3)cc2)c1 Show InChI InChI=1S/C18H20N2O4/c21-20(22)15-4-3-5-18(14-15)24-17-8-6-16(7-9-17)23-13-12-19-10-1-2-11-19/h3-9,14H,1-2,10-13H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Homo sapiens (Human))	BDBM50343920 (4-(4-(2-(Pyrrolidin-1-yl)ethoxy)phenoxy)aniline | ...) Show SMILES Nc1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C18H22N2O2/c19-15-3-5-17(6-4-15)22-18-9-7-16(8-10-18)21-14-13-20-11-1-2-12-20/h3-10H,1-2,11-14,19H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of purified COX1 assessed as formation of oxidized TMPD during reduction og PGG2 to PGH2 preincubated for 15 mins by chromogenic assay				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343914 (1-(2-(4-(4-(Trifluoromethyl)phenoxy)phenoxy)ethyl)...) Show SMILES FC(F)(F)c1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C19H20F3NO2/c20-19(21,22)15-3-5-17(6-4-15)25-18-9-7-16(8-10-18)24-14-13-23-11-1-2-12-23/h3-10H,1-2,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343923 (CHEMBL1775110 | N-(4-(4-(2-(Pyrrolidin-1-yl)ethoxy...) Show SMILES CS(=O)(=O)Nc1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C19H24N2O4S/c1-26(22,23)20-16-4-6-18(7-5-16)25-19-10-8-17(9-11-19)24-15-14-21-12-2-3-13-21/h4-11,20H,2-3,12-15H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343911 (3-Nitro-2-(4-(2-(pyrrolidin-1-yl)ethoxy)phenoxy)py...) Show SMILES [O-][N+](=O)c1cccnc1Oc1ccc(OCCN2CCCC2)cc1 Show InChI InChI=1S/C17H19N3O4/c21-20(22)16-4-3-9-18-17(16)24-15-7-5-14(6-8-15)23-13-12-19-10-1-2-11-19/h3-9H,1-2,10-13H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343923 (CHEMBL1775110 | N-(4-(4-(2-(Pyrrolidin-1-yl)ethoxy...) Show SMILES CS(=O)(=O)Nc1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C19H24N2O4S/c1-26(22,23)20-16-4-6-18(7-5-16)25-19-10-8-17(9-11-19)24-15-14-21-12-2-3-13-21/h4-11,20H,2-3,12-15H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343910 (2-(4-(2-(Pyrrolidin-1-yl)ethoxy)phenoxy)pyrazine |...) Show SMILES C(CN1CCCC1)Oc1ccc(Oc2cnccn2)cc1 Show InChI InChI=1S/C16H19N3O2/c1-2-10-19(9-1)11-12-20-14-3-5-15(6-4-14)21-16-13-17-7-8-18-16/h3-8,13H,1-2,9-12H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50343912 (1-(2-(4-(2-(Trifluoromethyl)phenoxy)phenoxy)ethyl)...) Show SMILES FC(F)(F)c1ccccc1Oc1ccc(OCCN2CCCC2)cc1 Show InChI InChI=1S/C19H20F3NO2/c20-19(21,22)17-5-1-2-6-18(17)25-16-9-7-15(8-10-16)24-14-13-23-11-3-4-12-23/h1-2,5-10H,3-4,11-14H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of COX2 in human whole blood assessed as inhibition of LPS-induced PGE2 production after 24 hrs by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50343917 (1-(2-(4-(4-Bromophenoxy)phenoxy)ethyl)pyrrolidine ...) Show SMILES Brc1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C18H20BrNO2/c19-15-3-5-17(6-4-15)22-18-9-7-16(8-10-18)21-14-13-20-11-1-2-12-20/h3-10H,1-2,11-14H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of COX2 in human whole blood assessed as inhibition of LPS-induced PGE2 production after 24 hrs by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343925 (1-(2-(4-(2-Nitrophenoxy)-phenoxy)ethyl)pyrrolidine...) Show SMILES [O-][N+](=O)c1ccccc1Oc1ccc(OCCN2CCCC2)cc1 Show InChI InChI=1S/C18H20N2O4/c21-20(22)17-5-1-2-6-18(17)24-16-9-7-15(8-10-16)23-14-13-19-11-3-4-12-19/h1-2,5-10H,3-4,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50343925 (1-(2-(4-(2-Nitrophenoxy)-phenoxy)ethyl)pyrrolidine...) Show SMILES [O-][N+](=O)c1ccccc1Oc1ccc(OCCN2CCCC2)cc1 Show InChI InChI=1S/C18H20N2O4/c21-20(22)17-5-1-2-6-18(17)24-16-9-7-15(8-10-16)23-14-13-19-11-3-4-12-19/h1-2,5-10H,3-4,11-14H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of purified COX2 assessed as formation of oxidized TMPD during reduction og PGG2 to PGH2 preincubated for 15 mins by chromogenic assay				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50343925 (1-(2-(4-(2-Nitrophenoxy)-phenoxy)ethyl)pyrrolidine...) Show SMILES [O-][N+](=O)c1ccccc1Oc1ccc(OCCN2CCCC2)cc1 Show InChI InChI=1S/C18H20N2O4/c21-20(22)17-5-1-2-6-18(17)24-16-9-7-15(8-10-16)23-14-13-19-11-3-4-12-19/h1-2,5-10H,3-4,11-14H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of COX2 in human whole blood assessed as inhibition of LPS-induced PGE2 production after 24 hrs by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50056999 (CHEMBL56367 | nimesulide) Show SMILES CS(=O)(=O)Nc1ccc(cc1Oc1ccccc1)[N+]([O-])=O Show InChI InChI=1S/C13H12N2O5S/c1-21(18,19)14-12-8-7-10(15(16)17)9-13(12)20-11-5-3-2-4-6-11/h2-9,14H,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	DrugBank Article PubMed	n/a	n/a	8.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of COX2 in human whole blood assessed as inhibition of LPS-induced PGE2 production after 24 hrs by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50343926 (1-(2-(4-(3-Nitrophenoxy)phenoxy)ethyl)pyrrolidine ...) Show SMILES [O-][N+](=O)c1cccc(Oc2ccc(OCCN3CCCC3)cc2)c1 Show InChI InChI=1S/C18H20N2O4/c21-20(22)15-4-3-5-18(14-15)24-17-8-6-16(7-9-17)23-13-12-19-10-1-2-11-19/h3-9,14H,1-2,10-13H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of COX2 in human whole blood assessed as inhibition of LPS-induced PGE2 production after 24 hrs by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Homo sapiens (Human))	BDBM50343927 (1-(2-(4-(4-Nitrophenoxy)phenoxy)ethyl)pyrrolidine ...) Show SMILES [O-][N+](=O)c1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C18H20N2O4/c21-20(22)15-3-5-17(6-4-15)24-18-9-7-16(8-10-18)23-14-13-19-11-1-2-12-19/h3-10H,1-2,11-14H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.04E+4	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of purified COX1 assessed as formation of oxidized TMPD during reduction og PGG2 to PGH2 preincubated for 15 mins by chromogenic assay				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50343916 (1-(2-(4-(4-Chlorophenoxy)phenoxy)ethyl)pyrrolidine...) Show SMILES Clc1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C18H20ClNO2/c19-15-3-5-17(6-4-15)22-18-9-7-16(8-10-18)21-14-13-20-11-1-2-12-20/h3-10H,1-2,11-14H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of COX2 in human whole blood assessed as inhibition of LPS-induced PGE2 production after 24 hrs by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Homo sapiens (Human))	BDBM50056999 (CHEMBL56367 | nimesulide) Show SMILES CS(=O)(=O)Nc1ccc(cc1Oc1ccccc1)[N+]([O-])=O Show InChI InChI=1S/C13H12N2O5S/c1-21(18,19)14-12-8-7-10(15(16)17)9-13(12)20-11-5-3-2-4-6-11/h2-9,14H,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	3.22E+4	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of purified COX1 assessed as formation of oxidized TMPD during reduction og PGG2 to PGH2 preincubated for 15 mins by chromogenic assay				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair				3D Structure (crystal)
Leukotriene A-4 hydrolase (Homo sapiens (Human))	BDBM50343911 (3-Nitro-2-(4-(2-(pyrrolidin-1-yl)ethoxy)phenoxy)py...) Show SMILES [O-][N+](=O)c1cccnc1Oc1ccc(OCCN2CCCC2)cc1 Show InChI InChI=1S/C17H19N3O4/c21-20(22)16-4-3-9-18-17(16)24-15-7-5-14(6-8-15)23-13-12-19-10-1-2-11-19/h3-9H,1-2,10-13H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of human LTA4 hydrolase activity assessed as LTB4 production after 15 mins by ELISA				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50343904 (2-(4-(2-(Pyrrolidin-1-yl)ethoxy)phenoxy)pyridine |...) Show SMILES C(CN1CCCC1)Oc1ccc(Oc2ccccn2)cc1 Show InChI InChI=1S/C17H20N2O2/c1-2-10-18-17(5-1)21-16-8-6-15(7-9-16)20-14-13-19-11-3-4-12-19/h1-2,5-10H,3-4,11-14H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.44E+4	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of purified COX2 assessed as formation of oxidized TMPD during reduction og PGG2 to PGH2 preincubated for 15 mins by chromogenic assay				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50343927 (1-(2-(4-(4-Nitrophenoxy)phenoxy)ethyl)pyrrolidine ...) Show SMILES [O-][N+](=O)c1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C18H20N2O4/c21-20(22)15-3-5-17(6-4-15)24-18-9-7-16(8-10-18)23-14-13-19-11-1-2-12-19/h3-10H,1-2,11-14H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.53E+4	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of purified COX2 assessed as formation of oxidized TMPD during reduction og PGG2 to PGH2 preincubated for 15 mins by chromogenic assay				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50343920 (4-(4-(2-(Pyrrolidin-1-yl)ethoxy)phenoxy)aniline | ...) Show SMILES Nc1ccc(Oc2ccc(OCCN3CCCC3)cc2)cc1 Show InChI InChI=1S/C18H22N2O2/c19-15-3-5-17(6-4-15)22-18-9-7-16(8-10-18)21-14-13-20-11-1-2-12-20/h3-10H,1-2,11-14,19H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.63E+4	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of purified COX2 assessed as formation of oxidized TMPD during reduction og PGG2 to PGH2 preincubated for 15 mins by chromogenic assay				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50343912 (1-(2-(4-(2-(Trifluoromethyl)phenoxy)phenoxy)ethyl)...) Show SMILES FC(F)(F)c1ccccc1Oc1ccc(OCCN2CCCC2)cc1 Show InChI InChI=1S/C19H20F3NO2/c20-19(21,22)17-5-1-2-6-18(17)25-16-9-7-15(8-10-16)24-14-13-23-11-3-4-12-23/h1-2,5-10H,3-4,11-14H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.14E+4	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of purified COX2 assessed as formation of oxidized TMPD during reduction og PGG2 to PGH2 preincubated for 15 mins by chromogenic assay				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Homo sapiens (Human))	BDBM50343925 (1-(2-(4-(2-Nitrophenoxy)-phenoxy)ethyl)pyrrolidine...) Show SMILES [O-][N+](=O)c1ccccc1Oc1ccc(OCCN2CCCC2)cc1 Show InChI InChI=1S/C18H20N2O4/c21-20(22)17-5-1-2-6-18(17)24-16-9-7-15(8-10-16)23-14-13-19-11-3-4-12-19/h1-2,5-10H,3-4,11-14H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Peking University Curated by ChEMBL					Assay Description Inhibition of purified COX1 assessed as formation of oxidized TMPD during reduction og PGG2 to PGH2 preincubated for 15 mins by chromogenic assay				J Med Chem 54: 3650-60 (2011) Article DOI: 10.1021/jm200063s BindingDB Entry DOI: 10.7270/Q24M94WS
					More data for this Ligand-Target Pair

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