null

SMILES: CN1CN(CC(=O)OC(C)(C)C)C(=O)N(CC(=O)OC(C)(C)C)[C@@H](Cc2ccccc2)C1=O

InChI Key: InChIKey=ZHQPYUNBQDKSPL-SFHVURJKSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50200326   

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
Group 10 secretory phospholipase A2 (Homo sapiens (Human))	BDBM50200326 (((S)-7-benzyl-3-tert-butoxycarbonylmethyl-5-methyl...) Show SMILES CN1CN(CC(=O)OC(C)(C)C)C(=O)N(CC(=O)OC(C)(C)C)[C@@H](Cc2ccccc2)C1=O Show InChI InChI=1S/C24H35N3O6/c1-23(2,3)32-19(28)14-26-16-25(7)21(30)18(13-17-11-9-8-10-12-17)27(22(26)31)15-20(29)33-24(4,5)6/h8-12,18H,13-16H2,1-7H3/t18-/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
Phospholipase A2 group V (Homo sapiens (Human))	BDBM50200326 (((S)-7-benzyl-3-tert-butoxycarbonylmethyl-5-methyl...) Show SMILES CN1CN(CC(=O)OC(C)(C)C)C(=O)N(CC(=O)OC(C)(C)C)[C@@H](Cc2ccccc2)C1=O Show InChI InChI=1S/C24H35N3O6/c1-23(2,3)32-19(28)14-26-16-25(7)21(30)18(13-17-11-9-8-10-12-17)27(22(26)31)15-20(29)33-24(4,5)6/h8-12,18H,13-16H2,1-7H3/t18-/m0/s1	KEGG UniProtKB/SwissProt antibodypedia 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 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