Compile Data Set for Download or QSAR

Found 14 hits Enz. Inhib. hit(s) with Target = 'Group IID secretory phospholipase A2' AND taxid = 10090   

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
Group IID secretory phospholipase A2 (Mus musculus)	BDBM50263002 ((2-amino-2-oxoacetyl)-1-benzyl-2-ethyl-1H-6,7-benz...) Show SMILES CCc1c(C(=O)C(N)=O)c2c(OCC(O)=O)cc3ccccc3c2n1Cc1ccccc1 Show InChI InChI=1S/C25H22N2O5/c1-2-18-21(24(30)25(26)31)22-19(32-14-20(28)29)12-16-10-6-7-11-17(16)23(22)27(18)13-15-8-4-3-5-9-15/h3-12H,2,13-14H2,1H3,(H2,26,31)(H,28,29)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	320	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of mouse group2D phospholipase A2 fluorimetric assay				J Med Chem 51: 4708-14 (2008) Article DOI: 10.1021/jm800422v BindingDB Entry DOI: 10.7270/Q2571BSD
					More data for this Ligand-Target Pair
Group IID secretory phospholipase A2 (Mus musculus)	BDBM50055366 ((3-Aminooxalyl-1-benzyl-2-ethyl-1H-indol-4-yloxy)-...) Show SMILES CCc1c(C(=O)C(N)=O)c2c(OCC(O)=O)cccc2n1Cc1ccccc1 Show InChI InChI=1S/C21H20N2O5/c1-2-14-19(20(26)21(22)27)18-15(9-6-10-16(18)28-12-17(24)25)23(14)11-13-7-4-3-5-8-13/h3-10H,2,11-12H2,1H3,(H2,22,27)(H,24,25)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	430	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of mouse group2D phospholipase A2 fluorimetric assay				J Med Chem 51: 4708-14 (2008) Article DOI: 10.1021/jm800422v BindingDB Entry DOI: 10.7270/Q2571BSD
					More data for this Ligand-Target Pair
Group IID secretory phospholipase A2 (Mus musculus)	BDBM50263001 (2-(1-benzyl-2-isobutyl-1H-6,7-benzoindol-4-yloxy)-...) Show SMILES CC(C)Cc1c(C(=O)C(N)=O)c2c(OCC(=O)NS(=O)(=O)c3ccccc3)cc3ccccc3c2n1Cc1ccccc1 Show InChI InChI=1S/C33H31N3O6S/c1-21(2)17-26-29(32(38)33(34)39)30-27(42-20-28(37)35-43(40,41)24-14-7-4-8-15-24)18-23-13-9-10-16-25(23)31(30)36(26)19-22-11-5-3-6-12-22/h3-16,18,21H,17,19-20H2,1-2H3,(H2,34,39)(H,35,37)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	530	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of mouse group2D phospholipase A2 fluorimetric assay				J Med Chem 51: 4708-14 (2008) Article DOI: 10.1021/jm800422v BindingDB Entry DOI: 10.7270/Q2571BSD
					More data for this Ligand-Target Pair
Group IID secretory phospholipase A2 (Mus musculus)	BDBM50262804 (2-(3-(2-amino-2-oxoacetyl)-1-benzyl-2-isobutyl-1H-...) Show SMILES CC(C)Cc1c(C(=O)C(N)=O)c2c(OCC(O)=O)cc3ccccc3c2n1Cc1ccccc1 Show InChI InChI=1S/C27H26N2O5/c1-16(2)12-20-23(26(32)27(28)33)24-21(34-15-22(30)31)13-18-10-6-7-11-19(18)25(24)29(20)14-17-8-4-3-5-9-17/h3-11,13,16H,12,14-15H2,1-2H3,(H2,28,33)(H,30,31)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	640	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of mouse group2D phospholipase A2 fluorimetric assay				J Med Chem 51: 4708-14 (2008) Article DOI: 10.1021/jm800422v BindingDB Entry DOI: 10.7270/Q2571BSD
					More data for this Ligand-Target Pair
Group IID secretory phospholipase A2 (Mus musculus)	BDBM50262842 (Benzenesulfonyl-2-(3-(2-amino-2-oxoacetyl)-1-benzy...) Show SMILES CCc1c(C(=O)C(N)=O)c2c(OCC(=O)NS(=O)(=O)c3ccccc3)cccc2n1Cc1ccccc1 Show InChI InChI=1S/C27H25N3O6S/c1-2-20-25(26(32)27(28)33)24-21(30(20)16-18-10-5-3-6-11-18)14-9-15-22(24)36-17-23(31)29-37(34,35)19-12-7-4-8-13-19/h3-15H,2,16-17H2,1H3,(H2,28,33)(H,29,31)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	890	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of mouse group2D phospholipase A2 fluorimetric assay				J Med Chem 51: 4708-14 (2008) Article DOI: 10.1021/jm800422v BindingDB Entry DOI: 10.7270/Q2571BSD
					More data for this Ligand-Target Pair
Group IID secretory phospholipase A2 (Mus musculus)	BDBM50263000 (2-(1-benzyl-2-ethyl-1H-6,7-benzoindol-4-yloxy)-N-(...) Show SMILES CCc1c(C(=O)C(N)=O)c2c(OCC(=O)NS(=O)(=O)c3ccccc3)cc3ccccc3c2n1Cc1ccccc1 Show InChI InChI=1S/C31H27N3O6S/c1-2-24-27(30(36)31(32)37)28-25(40-19-26(35)33-41(38,39)22-14-7-4-8-15-22)17-21-13-9-10-16-23(21)29(28)34(24)18-20-11-5-3-6-12-20/h3-17H,2,18-19H2,1H3,(H2,32,37)(H,33,35)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of mouse group2D phospholipase A2 fluorimetric assay				J Med Chem 51: 4708-14 (2008) Article DOI: 10.1021/jm800422v BindingDB Entry DOI: 10.7270/Q2571BSD
					More data for this Ligand-Target Pair
Group IID secretory phospholipase A2 (Mus musculus)	BDBM50262844 (2-(3-(2-amino-2-oxoacetyl)-1-benzyl-2-isobutyl-1H-...) Show SMILES CC(C)Cc1c(C(=O)C(N)=O)c2c(OCC(O)=O)cccc2n1Cc1ccccc1 Show InChI InChI=1S/C23H24N2O5/c1-14(2)11-17-21(22(28)23(24)29)20-16(9-6-10-18(20)30-13-19(26)27)25(17)12-15-7-4-3-5-8-15/h3-10,14H,11-13H2,1-2H3,(H2,24,29)(H,26,27)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of mouse group2D phospholipase A2 fluorimetric assay				J Med Chem 51: 4708-14 (2008) Article DOI: 10.1021/jm800422v BindingDB Entry DOI: 10.7270/Q2571BSD
					More data for this Ligand-Target Pair
Group IID secretory phospholipase A2 (Mus musculus)	BDBM50263003 (2-(2-ethyl-3-(o-phenylbenzyl)-8-(2-oxopropoxy)indo...) Show SMILES CCc1c(C(=O)C(N)=O)c2c(OC)cc3ccccc3c2n1Cc1ccccc1 Show InChI InChI=1S/C24H22N2O3/c1-3-18-20(23(27)24(25)28)21-19(29-2)13-16-11-7-8-12-17(16)22(21)26(18)14-15-9-5-4-6-10-15/h4-13H,3,14H2,1-2H3,(H2,25,28)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of mouse group2D phospholipase A2 fluorimetric assay				J Med Chem 51: 4708-14 (2008) Article DOI: 10.1021/jm800422v BindingDB Entry DOI: 10.7270/Q2571BSD
					More data for this Ligand-Target Pair
Group IID secretory phospholipase A2 (Mus musculus)	BDBM50262843 (Benzenesulfonyl-2-(3-(2-amino-2-oxoacetyl)-1-benzy...) Show SMILES CC(C)Cc1c(C(=O)C(N)=O)c2c(OCC(=O)NS(=O)(=O)c3ccccc3)cccc2n1Cc1ccccc1 Show InChI InChI=1S/C29H29N3O6S/c1-19(2)16-23-27(28(34)29(30)35)26-22(32(23)17-20-10-5-3-6-11-20)14-9-15-24(26)38-18-25(33)31-39(36,37)21-12-7-4-8-13-21/h3-15,19H,16-18H2,1-2H3,(H2,30,35)(H,31,33)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of mouse group2D phospholipase A2 fluorimetric assay				J Med Chem 51: 4708-14 (2008) Article DOI: 10.1021/jm800422v BindingDB Entry DOI: 10.7270/Q2571BSD
					More data for this Ligand-Target Pair
Group IID secretory phospholipase A2 (Mus musculus)	BDBM50263053 (2-(3-Biphenyl-2-ylmethyl-2-ethyl-8-methoxy-indoliz...) Show SMILES CCc1c(Cc2ccccc2-c2ccccc2)n2cccc(OC)c2c1C(=O)C(N)=O Show InChI InChI=1S/C26H24N2O3/c1-3-19-21(16-18-12-7-8-13-20(18)17-10-5-4-6-11-17)28-15-9-14-22(31-2)24(28)23(19)25(29)26(27)30/h4-15H,3,16H2,1-2H3,(H2,27,30)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of mouse group2D phospholipase A2 fluorimetric assay				J Med Chem 51: 4708-14 (2008) Article DOI: 10.1021/jm800422v BindingDB Entry DOI: 10.7270/Q2571BSD
					More data for this Ligand-Target Pair
Group IID secretory phospholipase A2 (Mus musculus)	BDBM50263052 (2-[3-Biphenyl-2-ylmethyl-2-ethyl-8-(2-oxo-propoxy)...) Show SMILES CCc1c(Cc2ccccc2-c2ccccc2)n2cccc(OCC(C)=O)c2c1C(=O)C(N)=O Show InChI InChI=1S/C28H26N2O4/c1-3-21-23(16-20-12-7-8-13-22(20)19-10-5-4-6-11-19)30-15-9-14-24(34-17-18(2)31)26(30)25(21)27(32)28(29)33/h4-15H,3,16-17H2,1-2H3,(H2,29,33)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of mouse group2D phospholipase A2 fluorimetric assay				J Med Chem 51: 4708-14 (2008) Article DOI: 10.1021/jm800422v BindingDB Entry DOI: 10.7270/Q2571BSD
					More data for this Ligand-Target Pair
Group IID secretory phospholipase A2 (Mus musculus)	BDBM50263051 (2-(1-(2-amino-2-oxoacetyl)-2-(isobutyl)-3-(ophenyl...) Show SMILES CC(C)Cc1c(Cc2ccccc2-c2ccccc2)n2cccc(OCC(O)=O)c2c1C(=O)C(N)=O Show InChI InChI=1S/C29H28N2O5/c1-18(2)15-22-23(16-20-11-6-7-12-21(20)19-9-4-3-5-10-19)31-14-8-13-24(36-17-25(32)33)27(31)26(22)28(34)29(30)35/h3-14,18H,15-17H2,1-2H3,(H2,30,35)(H,32,33)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of mouse group2D phospholipase A2 fluorimetric assay				J Med Chem 51: 4708-14 (2008) Article DOI: 10.1021/jm800422v BindingDB Entry DOI: 10.7270/Q2571BSD
					More data for this Ligand-Target Pair
Group IID secretory phospholipase A2 (Mus musculus)	BDBM50053137 ((1-Aminooxalyl-3-biphenyl-2-ylmethyl-2-ethyl-indol...) Show SMILES CCc1c(Cc2ccccc2-c2ccccc2)n2cccc(OCC(O)=O)c2c1C(=O)C(N)=O Show InChI InChI=1S/C27H24N2O5/c1-2-19-21(15-18-11-6-7-12-20(18)17-9-4-3-5-10-17)29-14-8-13-22(34-16-23(30)31)25(29)24(19)26(32)27(28)33/h3-14H,2,15-16H2,1H3,(H2,28,33)(H,30,31)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of mouse group2D phospholipase A2 fluorimetric assay				J Med Chem 51: 4708-14 (2008) Article DOI: 10.1021/jm800422v BindingDB Entry DOI: 10.7270/Q2571BSD
					More data for this Ligand-Target Pair
Group IID secretory phospholipase A2 (Mus musculus)	BDBM50055391 (2-(3-(2-amino-2-oxoacetyl)-1-benzyl-2-ethyl-1H-ind...) Show SMILES CCc1c(C(=O)C(N)=O)c2c(OC(C)C(O)=O)cccc2n1Cc1ccccc1 Show InChI InChI=1S/C22H22N2O5/c1-3-15-19(20(25)21(23)26)18-16(24(15)12-14-8-5-4-6-9-14)10-7-11-17(18)29-13(2)22(27)28/h4-11,13H,3,12H2,1-2H3,(H2,23,26)(H,27,28)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Washington Curated by ChEMBL					Assay Description Inhibition of mouse group2D phospholipase A2 fluorimetric assay				J Med Chem 51: 4708-14 (2008) Article DOI: 10.1021/jm800422v BindingDB Entry DOI: 10.7270/Q2571BSD
					More data for this Ligand-Target Pair