Compile Data Set for Download or QSAR

Found 29 hits with Last Name = 'ferrándiz' and Initial = 'ml'   

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
Polyunsaturated fatty acid 5-lipoxygenase (Homo sapiens (Human))	BDBM50250926 (1-ethyl-6-((3-fluoro-5-(4-methoxytetrahydro-2H-pyr...) Show SMILES CCn1c2ccc(COc3cc(F)cc(c3)C3(CCOCC3)OC)cc2ccc1=O Show InChI InChI=1S/C24H26FNO4/c1-3-26-22-6-4-17(12-18(22)5-7-23(26)27)16-30-21-14-19(13-20(25)15-21)24(28-2)8-10-29-11-9-24/h4-7,12-15H,3,8-11,16H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	n/a	n/a
Universidad de Valencia Curated by ChEMBL					Assay Description Inhibitory concentration required against 5-lipoxygenase activity in intact cells of human neutrophils				Bioorg Med Chem Lett 8: 1169-74 (1999) BindingDB Entry DOI: 10.7270/Q20865S1
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Homo sapiens (Human))	BDBM50250926 (1-ethyl-6-((3-fluoro-5-(4-methoxytetrahydro-2H-pyr...) Show SMILES CCn1c2ccc(COc3cc(F)cc(c3)C3(CCOCC3)OC)cc2ccc1=O Show InChI InChI=1S/C24H26FNO4/c1-3-26-22-6-4-17(12-18(22)5-7-23(26)27)16-30-21-14-19(13-20(25)15-21)24(28-2)8-10-29-11-9-24/h4-7,12-15H,3,8-11,16H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	90	n/a	n/a	n/a	n/a	n/a	n/a
Universidad de Valencia Curated by ChEMBL					Assay Description Inhibitory concentration required against 5-lipoxygenase activity in cytosolic fractions of human neutrophils				Bioorg Med Chem Lett 8: 1169-74 (1999) BindingDB Entry DOI: 10.7270/Q20865S1
					More data for this Ligand-Target Pair
Phospholipase A2, membrane associated (Homo sapiens (Human))	BDBM50259952 (CHEMBL480874 | cacospongionolide E) Show SMILES C[C@H]1CC[C@]2(C)[C@H](CCC=C2C)[C@@]1(C)CCC1=CC[C@@H](OC1)C1=CC(=O)O[C@H]1O |r,c:9,t:18,25| Show InChI InChI=1S/C25H36O4/c1-16-6-5-7-21-24(16,3)12-10-17(2)25(21,4)13-11-18-8-9-20(28-15-18)19-14-22(26)29-23(19)27/h6,8,14,17,20-21,23,27H,5,7,9-13,15H2,1-4H3/t17-,20+,21-,23+,24-,25-/m0/s1	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	1.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of human synovial group2 sPLA2 by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Phospholipase A2 (Apis mellifera)	BDBM50259951 (CHEMBL480681 | cacospongionolide) Show SMILES C[C@H]1CC[C@@]23C[C@]2(C)CCC[C@@H]3[C@@]1(C)CCC1=CC[C@@H](OC1)C1=CC(=O)O[C@H]1O |r,t:19,26| Show InChI InChI=1S/C25H36O4/c1-16-8-12-25-15-23(25,2)10-4-5-20(25)24(16,3)11-9-17-6-7-19(28-14-17)18-13-21(26)29-22(18)27/h6,13,16,19-20,22,27H,4-5,7-12,14-15H2,1-3H3/t16-,19+,20+,22+,23-,24-,25-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of bee venom group3 sPLA2 by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Phospholipase A2 (Apis mellifera)	BDBM50259951 (CHEMBL480681 | cacospongionolide) Show SMILES C[C@H]1CC[C@@]23C[C@]2(C)CCC[C@@H]3[C@@]1(C)CCC1=CC[C@@H](OC1)C1=CC(=O)O[C@H]1O |r,t:19,26| Show InChI InChI=1S/C25H36O4/c1-16-8-12-25-15-23(25,2)10-4-5-20(25)24(16,3)11-9-17-6-7-19(28-14-17)18-13-21(26)29-22(18)27/h6,13,16,19-20,22,27H,4-5,7-12,14-15H2,1-3H3/t16-,19+,20+,22+,23-,24-,25-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of bee venom group3 sPLA2 by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Phospholipase A2, membrane associated (Homo sapiens (Human))	BDBM50259951 (CHEMBL480681 | cacospongionolide) Show SMILES C[C@H]1CC[C@@]23C[C@]2(C)CCC[C@@H]3[C@@]1(C)CCC1=CC[C@@H](OC1)C1=CC(=O)O[C@H]1O |r,t:19,26| Show InChI InChI=1S/C25H36O4/c1-16-8-12-25-15-23(25,2)10-4-5-20(25)24(16,3)11-9-17-6-7-19(28-14-17)18-13-21(26)29-22(18)27/h6,13,16,19-20,22,27H,4-5,7-12,14-15H2,1-3H3/t16-,19+,20+,22+,23-,24-,25-/m0/s1	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	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of human synovial group2 sPLA2 by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50029593 (CHEMBL7162 | N-(2-(cyclohexyloxy)-4-nitrophenyl)me...) Show SMILES CS(=O)(=O)Nc1ccc(cc1OC1CCCCC1)[N+]([O-])=O Show InChI InChI=1S/C13H18N2O5S/c1-21(18,19)14-12-8-7-10(15(16)17)9-13(12)20-11-5-3-2-4-6-11/h7-9,11,14H,2-6H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PDB PubMed	n/a	n/a	3.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universidad de Valencia Curated by ChEMBL					Assay Description Inhibitory concentration required against COX-2 activity in intact human monocytes				Bioorg Med Chem Lett 8: 1169-74 (1999) BindingDB Entry DOI: 10.7270/Q20865S1
					More data for this Ligand-Target Pair				3D Structure (crystal)
Polyunsaturated fatty acid 5-lipoxygenase (Homo sapiens (Human))	BDBM50070261 ((E)-3-(2-Chloro-quinolin-3-yl)-1-(2,4-dimethyl-fur...) Show SMILES Cc1coc(C)c1C(=O)C=Cc1cc2ccccc2nc1Cl |w:10.11| Show InChI InChI=1S/C18H14ClNO2/c1-11-10-22-12(2)17(11)16(21)8-7-14-9-13-5-3-4-6-15(13)20-18(14)19/h3-10H,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universidad de Valencia Curated by ChEMBL					Assay Description Inhibitory concentration required against 5-lipoxygenase activity in cytosolic fractions of human neutrophils				Bioorg Med Chem Lett 8: 1169-74 (1999) BindingDB Entry DOI: 10.7270/Q20865S1
					More data for this Ligand-Target Pair
Acidic phospholipase A2 2 (Naja naja)	BDBM50259951 (CHEMBL480681 | cacospongionolide) Show SMILES C[C@H]1CC[C@@]23C[C@]2(C)CCC[C@@H]3[C@@]1(C)CCC1=CC[C@@H](OC1)C1=CC(=O)O[C@H]1O |r,t:19,26| Show InChI InChI=1S/C25H36O4/c1-16-8-12-25-15-23(25,2)10-4-5-20(25)24(16,3)11-9-17-6-7-19(28-14-17)18-13-21(26)29-22(18)27/h6,13,16,19-20,22,27H,4-5,7-12,14-15H2,1-3H3/t16-,19+,20+,22+,23-,24-,25-/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of Naja naja venom group1 sPLA2 at 10 uM by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Phospholipase A2, membrane associated (Homo sapiens (Human))	BDBM50250399 (5-Hydroxy-4-{(R)-6-hydroxy-5-[(E)-4-methyl-6-(2,6,...) Show SMILES C\C(CCC1=C(C)CCCC1(C)C)=C/CCC1=CC[C@@H](O[C@H]1O)C1=CC(=O)O[C@H]1O |r,c:4,t:17,25| Show InChI InChI=1S/C25H36O5/c1-16(10-12-20-17(2)8-6-14-25(20,3)4)7-5-9-18-11-13-21(29-23(18)27)19-15-22(26)30-24(19)28/h7,11,15,21,23-24,27-28H,5-6,8-10,12-14H2,1-4H3/b16-7+/t21-,23-,24-/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of human synovial group2 sPLA2 by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Homo sapiens (Human))	BDBM50070263 ((E)-3-(2-Chloro-quinolin-3-yl)-1-(4-fluoro-phenyl)...) Show SMILES Fc1ccc(cc1)C(=O)\C=C\c1cc2ccccc2nc1Cl Show InChI InChI=1S/C18H11ClFNO/c19-18-14(11-13-3-1-2-4-16(13)21-18)7-10-17(22)12-5-8-15(20)9-6-12/h1-11H/b10-7+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universidad de Valencia Curated by ChEMBL					Assay Description Inhibitory concentration required against 5-lipoxygenase activity in cytosolic fractions of human neutrophils				Bioorg Med Chem Lett 8: 1169-74 (1999) BindingDB Entry DOI: 10.7270/Q20865S1
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Homo sapiens (Human))	BDBM50070260 ((E)-1-(3,4-Dichloro-phenyl)-3-furan-2-yl-propenone...) Show SMILES Clc1ccc(cc1Cl)C(=O)\C=C\c1ccco1 Show InChI InChI=1S/C13H8Cl2O2/c14-11-5-3-9(8-12(11)15)13(16)6-4-10-2-1-7-17-10/h1-8H/b6-4+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	4.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universidad de Valencia Curated by ChEMBL					Assay Description Inhibitory concentration required against 5-lipoxygenase activity in cytosolic fractions of human neutrophils				Bioorg Med Chem Lett 8: 1169-74 (1999) BindingDB Entry DOI: 10.7270/Q20865S1
					More data for this Ligand-Target Pair
Phospholipase A2, membrane associated (Homo sapiens (Human))	BDBM50377908 (CACOSPONGIONOLIDE B) Show SMILES C[C@@H]1CC[C@@]2(C)[C@@H](CCCC2=C)[C@]1(C)CCC1=CCC(OC1)C1=CC(=O)OC1O |t:18,25| Show InChI InChI=1S/C25H36O4/c1-16-6-5-7-21-24(16,3)12-10-17(2)25(21,4)13-11-18-8-9-20(28-15-18)19-14-22(26)29-23(19)27/h8,14,17,20-21,23,27H,1,5-7,9-13,15H2,2-4H3/t17-,20?,21-,23?,24-,25-/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of human synovial group2 sPLA2 by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Homo sapiens (Human))	BDBM50070259 ((E)-1-(4-Bromo-phenyl)-3-(2,3-dimethoxy-phenyl)-pr...) Show SMILES COc1cccc(\C=C\C(=O)c2ccc(Br)cc2)c1OC Show InChI InChI=1S/C17H15BrO3/c1-20-16-5-3-4-13(17(16)21-2)8-11-15(19)12-6-9-14(18)10-7-12/h3-11H,1-2H3/b11-8+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	6.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universidad de Valencia Curated by ChEMBL					Assay Description Inhibitory concentration required against 5-lipoxygenase activity in cytosolic fractions of human neutrophils				Bioorg Med Chem Lett 8: 1169-74 (1999) BindingDB Entry DOI: 10.7270/Q20865S1
					More data for this Ligand-Target Pair
Phospholipase A2 (Apis mellifera)	BDBM50250399 (5-Hydroxy-4-{(R)-6-hydroxy-5-[(E)-4-methyl-6-(2,6,...) Show SMILES C\C(CCC1=C(C)CCCC1(C)C)=C/CCC1=CC[C@@H](O[C@H]1O)C1=CC(=O)O[C@H]1O |r,c:4,t:17,25| Show InChI InChI=1S/C25H36O5/c1-16(10-12-20-17(2)8-6-14-25(20,3)4)7-5-9-18-11-13-21(29-23(18)27)19-15-22(26)30-24(19)28/h7,11,15,21,23-24,27-28H,5-6,8-10,12-14H2,1-4H3/b16-7+/t21-,23-,24-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of bee venom group3 sPLA2 by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Phospholipase A2, membrane associated (Rattus norvegicus)	BDBM50259952 (CHEMBL480874 | cacospongionolide E) Show SMILES C[C@H]1CC[C@]2(C)[C@H](CCC=C2C)[C@@]1(C)CCC1=CC[C@@H](OC1)C1=CC(=O)O[C@H]1O |r,c:9,t:18,25| Show InChI InChI=1S/C25H36O4/c1-16-6-5-7-21-24(16,3)12-10-17(2)25(21,4)13-11-18-8-9-20(28-15-18)19-14-22(26)29-23(19)27/h6,8,14,17,20-21,23,27H,5,7,9-13,15H2,1-4H3/t17-,20+,21-,23+,24-,25-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of rat air pouch group2 sPLA2 by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Acidic phospholipase A2 2 (Naja naja)	BDBM50250399 (5-Hydroxy-4-{(R)-6-hydroxy-5-[(E)-4-methyl-6-(2,6,...) Show SMILES C\C(CCC1=C(C)CCCC1(C)C)=C/CCC1=CC[C@@H](O[C@H]1O)C1=CC(=O)O[C@H]1O |r,c:4,t:17,25| Show InChI InChI=1S/C25H36O5/c1-16(10-12-20-17(2)8-6-14-25(20,3)4)7-5-9-18-11-13-21(29-23(18)27)19-15-22(26)30-24(19)28/h7,11,15,21,23-24,27-28H,5-6,8-10,12-14H2,1-4H3/b16-7+/t21-,23-,24-/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of Naja naja venom group1 sPLA2 at 10 uM by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Phospholipase A2, membrane associated (Rattus norvegicus)	BDBM50259951 (CHEMBL480681 | cacospongionolide) Show SMILES C[C@H]1CC[C@@]23C[C@]2(C)CCC[C@@H]3[C@@]1(C)CCC1=CC[C@@H](OC1)C1=CC(=O)O[C@H]1O |r,t:19,26| Show InChI InChI=1S/C25H36O4/c1-16-8-12-25-15-23(25,2)10-4-5-20(25)24(16,3)11-9-17-6-7-19(28-14-17)18-13-21(26)29-22(18)27/h6,13,16,19-20,22,27H,4-5,7-12,14-15H2,1-3H3/t16-,19+,20+,22+,23-,24-,25-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.18E+4	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of rat air pouch group2 sPLA2 at 10 uM by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Phospholipase A2 (Apis mellifera)	BDBM50377908 (CACOSPONGIONOLIDE B) Show SMILES C[C@@H]1CC[C@@]2(C)[C@@H](CCCC2=C)[C@]1(C)CCC1=CCC(OC1)C1=CC(=O)OC1O |t:18,25| Show InChI InChI=1S/C25H36O4/c1-16-6-5-7-21-24(16,3)12-10-17(2)25(21,4)13-11-18-8-9-20(28-15-18)19-14-22(26)29-23(19)27/h8,14,17,20-21,23,27H,1,5-7,9-13,15H2,2-4H3/t17-,20?,21-,23?,24-,25-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.54E+4	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of bee venom group3 sPLA2 at 10 uM by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Phospholipase A2, membrane associated (Rattus norvegicus)	BDBM50377908 (CACOSPONGIONOLIDE B) Show SMILES C[C@@H]1CC[C@@]2(C)[C@@H](CCCC2=C)[C@]1(C)CCC1=CCC(OC1)C1=CC(=O)OC1O |t:18,25| Show InChI InChI=1S/C25H36O4/c1-16-6-5-7-21-24(16,3)12-10-17(2)25(21,4)13-11-18-8-9-20(28-15-18)19-14-22(26)29-23(19)27/h8,14,17,20-21,23,27H,1,5-7,9-13,15H2,2-4H3/t17-,20?,21-,23?,24-,25-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.69E+4	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of rat air pouch group2 sPLA2 at 10 uM by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Phospholipase A2, membrane associated (Rattus norvegicus)	BDBM50250399 (5-Hydroxy-4-{(R)-6-hydroxy-5-[(E)-4-methyl-6-(2,6,...) Show SMILES C\C(CCC1=C(C)CCCC1(C)C)=C/CCC1=CC[C@@H](O[C@H]1O)C1=CC(=O)O[C@H]1O |r,c:4,t:17,25| Show InChI InChI=1S/C25H36O5/c1-16(10-12-20-17(2)8-6-14-25(20,3)4)7-5-9-18-11-13-21(29-23(18)27)19-15-22(26)30-24(19)28/h7,11,15,21,23-24,27-28H,5-6,8-10,12-14H2,1-4H3/b16-7+/t21-,23-,24-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.84E+4	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of rat air pouch group2 sPLA2 at 10 uM by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Phospholipase A2 (Apis mellifera)	BDBM50250399 (5-Hydroxy-4-{(R)-6-hydroxy-5-[(E)-4-methyl-6-(2,6,...) Show SMILES C\C(CCC1=C(C)CCCC1(C)C)=C/CCC1=CC[C@@H](O[C@H]1O)C1=CC(=O)O[C@H]1O |r,c:4,t:17,25| Show InChI InChI=1S/C25H36O5/c1-16(10-12-20-17(2)8-6-14-25(20,3)4)7-5-9-18-11-13-21(29-23(18)27)19-15-22(26)30-24(19)28/h7,11,15,21,23-24,27-28H,5-6,8-10,12-14H2,1-4H3/b16-7+/t21-,23-,24-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.25E+4	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of bee venom group3 sPLA2 at 10 uM by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Phospholipase A2, membrane associated (Rattus norvegicus)	BDBM50259952 (CHEMBL480874 | cacospongionolide E) Show SMILES C[C@H]1CC[C@]2(C)[C@H](CCC=C2C)[C@@]1(C)CCC1=CC[C@@H](OC1)C1=CC(=O)O[C@H]1O |r,c:9,t:18,25| Show InChI InChI=1S/C25H36O4/c1-16-6-5-7-21-24(16,3)12-10-17(2)25(21,4)13-11-18-8-9-20(28-15-18)19-14-22(26)29-23(19)27/h6,8,14,17,20-21,23,27H,5,7,9-13,15H2,1-4H3/t17-,20+,21-,23+,24-,25-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.51E+4	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of rat air pouch group2 sPLA2 at 10 uM by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Phospholipase A2, membrane associated (Homo sapiens (Human))	BDBM50377908 (CACOSPONGIONOLIDE B) Show SMILES C[C@@H]1CC[C@@]2(C)[C@@H](CCCC2=C)[C@]1(C)CCC1=CCC(OC1)C1=CC(=O)OC1O |t:18,25| Show InChI InChI=1S/C25H36O4/c1-16-6-5-7-21-24(16,3)12-10-17(2)25(21,4)13-11-18-8-9-20(28-15-18)19-14-22(26)29-23(19)27/h8,14,17,20-21,23,27H,1,5-7,9-13,15H2,2-4H3/t17-,20?,21-,23?,24-,25-/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.67E+4	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of human synovial group2 sPLA2 at 10 uM by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Phospholipase A2, membrane associated (Homo sapiens (Human))	BDBM50259951 (CHEMBL480681 | cacospongionolide) Show SMILES C[C@H]1CC[C@@]23C[C@]2(C)CCC[C@@H]3[C@@]1(C)CCC1=CC[C@@H](OC1)C1=CC(=O)O[C@H]1O |r,t:19,26| Show InChI InChI=1S/C25H36O4/c1-16-8-12-25-15-23(25,2)10-4-5-20(25)24(16,3)11-9-17-6-7-19(28-14-17)18-13-21(26)29-22(18)27/h6,13,16,19-20,22,27H,4-5,7-12,14-15H2,1-3H3/t16-,19+,20+,22+,23-,24-,25-/m0/s1	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	9.07E+4	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of human synovial group2 sPLA2 at 10 uM by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Phospholipase A2, membrane associated (Homo sapiens (Human))	BDBM50250399 (5-Hydroxy-4-{(R)-6-hydroxy-5-[(E)-4-methyl-6-(2,6,...) Show SMILES C\C(CCC1=C(C)CCCC1(C)C)=C/CCC1=CC[C@@H](O[C@H]1O)C1=CC(=O)O[C@H]1O |r,c:4,t:17,25| Show InChI InChI=1S/C25H36O5/c1-16(10-12-20-17(2)8-6-14-25(20,3)4)7-5-9-18-11-13-21(29-23(18)27)19-15-22(26)30-24(19)28/h7,11,15,21,23-24,27-28H,5-6,8-10,12-14H2,1-4H3/b16-7+/t21-,23-,24-/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.32E+4	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of human synovial group2 sPLA2 at 10 uM by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Phospholipase A2 (Apis mellifera)	BDBM50259952 (CHEMBL480874 | cacospongionolide E) Show SMILES C[C@H]1CC[C@]2(C)[C@H](CCC=C2C)[C@@]1(C)CCC1=CC[C@@H](OC1)C1=CC(=O)O[C@H]1O |r,c:9,t:18,25| Show InChI InChI=1S/C25H36O4/c1-16-6-5-7-21-24(16,3)12-10-17(2)25(21,4)13-11-18-8-9-20(28-15-18)19-14-22(26)29-23(19)27/h6,8,14,17,20-21,23,27H,5,7,9-13,15H2,1-4H3/t17-,20+,21-,23+,24-,25-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.48E+4	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of bee venom group3 sPLA2 at 10 uM by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Phospholipase A2 (Apis mellifera)	BDBM50259952 (CHEMBL480874 | cacospongionolide E) Show SMILES C[C@H]1CC[C@]2(C)[C@H](CCC=C2C)[C@@]1(C)CCC1=CC[C@@H](OC1)C1=CC(=O)O[C@H]1O |r,c:9,t:18,25| Show InChI InChI=1S/C25H36O4/c1-16-6-5-7-21-24(16,3)12-10-17(2)25(21,4)13-11-18-8-9-20(28-15-18)19-14-22(26)29-23(19)27/h6,8,14,17,20-21,23,27H,5,7,9-13,15H2,1-4H3/t17-,20+,21-,23+,24-,25-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.48E+4	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of bee venom group3 sPLA2 at 10 uM by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair
Phospholipase A2, membrane associated (Homo sapiens (Human))	BDBM50259952 (CHEMBL480874 | cacospongionolide E) Show SMILES C[C@H]1CC[C@]2(C)[C@H](CCC=C2C)[C@@]1(C)CCC1=CC[C@@H](OC1)C1=CC(=O)O[C@H]1O |r,c:9,t:18,25| Show InChI InChI=1S/C25H36O4/c1-16-6-5-7-21-24(16,3)12-10-17(2)25(21,4)13-11-18-8-9-20(28-15-18)19-14-22(26)29-23(19)27/h6,8,14,17,20-21,23,27H,5,7,9-13,15H2,1-4H3/t17-,20+,21-,23+,24-,25-/m0/s1	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	9.67E+4	n/a	n/a	n/a	n/a	n/a	n/a
Istituto per la Chimica di Molecole di Interesse Biologico CNR Curated by ChEMBL					Assay Description Inhibition of human synovial group2 sPLA2 at 10 uM by liquid scintillation counting				J Nat Prod 61: 931-5 (1998) Article DOI: 10.1021/np980122t BindingDB Entry DOI: 10.7270/Q2BK1D8H
					More data for this Ligand-Target Pair