BDBM50216593 3-chloro-N-((1R,2S)-2-(4-(2-((dimethylamino)methyl)-1H-imidazol-1-yl)benzamido)cyclopentyl)-1H-indole-6-carboxamide::CHEMBL234172

SMILES: CN(C)Cc1nccn1-c1ccc(cc1)C(=O)N[C@H]1CCC[C@H]1NC(=O)c1ccc2c(Cl)c[nH]c2c1

InChI Key: InChIKey=NRUWCJQSBJZAAA-XZOQPEGZSA-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 = 50216593   

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))	BDBM50216593 (3-chloro-N-((1R,2S)-2-(4-(2-((dimethylamino)methyl...) Show SMILES CN(C)Cc1nccn1-c1ccc(cc1)C(=O)N[C@H]1CCC[C@H]1NC(=O)c1ccc2c(Cl)c[nH]c2c1 Show InChI InChI=1S/C27H29ClN6O2/c1-33(2)16-25-29-12-13-34(25)19-9-6-17(7-10-19)26(35)31-22-4-3-5-23(22)32-27(36)18-8-11-20-21(28)15-30-24(20)14-18/h6-15,22-23,30H,3-5,16H2,1-2H3,(H,31,35)(H,32,36)/t22-,23+/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	7.10	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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