BDBM50055368 (3-Aminooxalyl-2-methyl-1-naphthalen-1-ylmethyl-1H-indol-4-yloxy)-acetic acid::CHEMBL357804

SMILES: Cc1c(C(=O)C(N)=O)c2c(OCC(O)=O)cccc2n1Cc1cccc2ccccc12

InChI Key: InChIKey=OCZWKLXXLNWSDH-UHFFFAOYSA-N

Data: 3 IC50

PDB links: 1 PDB ID matches this monomer.

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50055368   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Phospholipase A2, membrane associated (Homo sapiens (Human))	BDBM50055368 ((3-Aminooxalyl-2-methyl-1-naphthalen-1-ylmethyl-1H...) Show SMILES Cc1c(C(=O)C(N)=O)c2c(OCC(O)=O)cccc2n1Cc1cccc2ccccc12 Show InChI InChI=1S/C24H20N2O5/c1-14-21(23(29)24(25)30)22-18(10-5-11-19(22)31-13-20(27)28)26(14)12-16-8-4-7-15-6-2-3-9-17(15)16/h2-11H,12-13H2,1H3,(H2,25,30)(H,27,28)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Inhibition of human nonpancreatic secretory Phospholipase A2 through DOC/PC assay				J Med Chem 39: 5159-75 (1997) Article DOI: 10.1021/jm960487f BindingDB Entry DOI: 10.7270/Q22B8X54
					More data for this Ligand-Target Pair
Phospholipase A2 (Homo sapiens (Human))	BDBM50055368 ((3-Aminooxalyl-2-methyl-1-naphthalen-1-ylmethyl-1H...) Show SMILES Cc1c(C(=O)C(N)=O)c2c(OCC(O)=O)cccc2n1Cc1cccc2ccccc12 Show InChI InChI=1S/C24H20N2O5/c1-14-21(23(29)24(25)30)22-18(10-5-11-19(22)31-13-20(27)28)26(14)12-16-8-4-7-15-6-2-3-9-17(15)16/h2-11H,12-13H2,1H3,(H2,25,30)(H,27,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Compound was tested for inhibition of human secretory pancreatic Phospholipase A2				J Med Chem 39: 5159-75 (1997) Article DOI: 10.1021/jm960487f BindingDB Entry DOI: 10.7270/Q22B8X54
					More data for this Ligand-Target Pair
Phospholipase A2, membrane associated (Homo sapiens (Human))	BDBM50055368 ((3-Aminooxalyl-2-methyl-1-naphthalen-1-ylmethyl-1H...) Show SMILES Cc1c(C(=O)C(N)=O)c2c(OCC(O)=O)cccc2n1Cc1cccc2ccccc12 Show InChI InChI=1S/C24H20N2O5/c1-14-21(23(29)24(25)30)22-18(10-5-11-19(22)31-13-20(27)28)26(14)12-16-8-4-7-15-6-2-3-9-17(15)16/h2-11H,12-13H2,1H3,(H2,25,30)(H,27,28)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	9	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Inhibition of human nonpancreatic secretory Phospholipase A2 through chromogenic assay				J Med Chem 39: 5159-75 (1997) Article DOI: 10.1021/jm960487f BindingDB Entry DOI: 10.7270/Q22B8X54
					More data for this Ligand-Target Pair