BDBM50216621 CHEMBL232529::N-[(1S,2R)-2-[(3-chlorobenzene)amido]cyclopentyl]-4-(2-oxo-1,2-dihydropyridin-1-yl)benzamide

SMILES: Clc1cccc(c1)C(=O)N[C@@H]1CCC[C@@H]1NC(=O)c1ccc(cc1)-n1ccccc1=O

InChI Key: InChIKey=FRNBTMSUUBMYTQ-LEWJYISDSA-N

Data: 1 KI

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 1 hit for monomerid = 50216621   

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
Coagulation factor X (Homo sapiens (Human))	BDBM50216621 (CHEMBL232529 | N-[(1S,2R)-2-[(3-chlorobenzene)amid...) Show SMILES Clc1cccc(c1)C(=O)N[C@@H]1CCC[C@@H]1NC(=O)c1ccc(cc1)-n1ccccc1=O Show InChI InChI=1S/C24H22ClN3O3/c25-18-6-3-5-17(15-18)24(31)27-21-8-4-7-20(21)26-23(30)16-10-12-19(13-11-16)28-14-2-1-9-22(28)29/h1-3,5-6,9-15,20-21H,4,7-8H2,(H,26,30)(H,27,31)/t20-,21+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	1.19E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Company Curated by ChEMBL					Assay Description Inhibition of human factor 10a				Bioorg Med Chem Lett 17: 4419-27 (2007) Article DOI: 10.1016/j.bmcl.2007.06.029 BindingDB Entry DOI: 10.7270/Q2416XVV
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