null

SMILES: O=C(Nc1ccccc1C#N)c1cnn2ccccc12

InChI Key: InChIKey=SJTYXICMAFQVBM-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50311292   

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))	BDBM50311292 (CHEMBL1077512 | N-(2-cyanophenyl)pyrazolo[1,5-a]py...) Show SMILES O=C(Nc1ccccc1C#N)c1cnn2ccccc12 Show InChI InChI=1S/C15H10N4O/c16-9-11-5-1-2-6-13(11)18-15(20)12-10-17-19-8-4-3-7-14(12)19/h1-8,10H,(H,18,20)	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	2.00E+4	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