BDBM50311302 CHEMBL1078107::N-(2-chlorophenyl)-5-phenylpyrazolo[1,5-a]pyridine-3-carboxamide

SMILES: Clc1ccccc1NC(=O)c1cnn2ccc(cc12)-c1ccccc1

InChI Key: InChIKey=UHIOXDRSXMCQPL-UHFFFAOYSA-N

Data: 1 IC50

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 = 50311302   

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
Ephrin type-B receptor 3 (Homo sapiens (Human))	BDBM50311302 (CHEMBL1078107 | N-(2-chlorophenyl)-5-phenylpyrazol...) Show SMILES Clc1ccccc1NC(=O)c1cnn2ccc(cc12)-c1ccccc1 Show InChI InChI=1S/C20H14ClN3O/c21-17-8-4-5-9-18(17)23-20(25)16-13-22-24-11-10-15(12-19(16)24)14-6-2-1-3-7-14/h1-13H,(H,23,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	66	n/a	n/a	n/a	n/a	n/a	n/a
Harvard Medical School Curated by ChEMBL					Assay Description Inhibition of human recombinant EphB3 kinase-mediated BTK-peptide phosphorylation assessed as 33P incorporation after 30 mins by scintillation counti...				Bioorg Med Chem Lett 19: 6122-6 (2009) Article DOI: 10.1016/j.bmcl.2009.09.010 BindingDB Entry DOI: 10.7270/Q2T43T66
					More data for this Ligand-Target Pair