null

SMILES: CC(C)[C@@H]1NC(=O)N(CC(=O)OC(C)(C)C)CN(C)C1=O

InChI Key: InChIKey=FKJRHILIMLIDKO-NSHDSACASA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50200325   

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 group V (Homo sapiens (Human))	BDBM50200325 ((S)-tert-butyl 2-(6-isopropyl-1-methyl-4,7-dioxo-1...) Show SMILES CC(C)[C@@H]1NC(=O)N(CC(=O)OC(C)(C)C)CN(C)C1=O Show InChI InChI=1S/C14H25N3O4/c1-9(2)11-12(19)16(6)8-17(13(20)15-11)7-10(18)21-14(3,4)5/h9,11H,7-8H2,1-6H3,(H,15,20)/t11-/m0/s1	KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
CNRS UMR 7175 Curated by ChEMBL					Assay Description Inhibition of human group 5 sPLA2				J Med Chem 49: 6768-78 (2006) Article DOI: 10.1021/jm0606589 BindingDB Entry DOI: 10.7270/Q2WH2PND
					More data for this Ligand-Target Pair
Group 10 secretory phospholipase A2 (Homo sapiens (Human))	BDBM50200325 ((S)-tert-butyl 2-(6-isopropyl-1-methyl-4,7-dioxo-1...) Show SMILES CC(C)[C@@H]1NC(=O)N(CC(=O)OC(C)(C)C)CN(C)C1=O Show InChI InChI=1S/C14H25N3O4/c1-9(2)11-12(19)16(6)8-17(13(20)15-11)7-10(18)21-14(3,4)5/h9,11H,7-8H2,1-6H3,(H,15,20)/t11-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
CNRS UMR 7175 Curated by ChEMBL					Assay Description Inhibition of human group 10 sPLA2				J Med Chem 49: 6768-78 (2006) Article DOI: 10.1021/jm0606589 BindingDB Entry DOI: 10.7270/Q2WH2PND
					More data for this Ligand-Target Pair