BDBM50195889 3-(pyridin-3-yl)-7-(3,4,5-trimethoxyphenyl)thieno[3,2-c]pyridin-4-amine::CHEMBL394384

SMILES: COc1cc(cc(OC)c1OC)-c1cnc(N)c2c(csc12)-c1cccnc1

InChI Key: InChIKey=UQHIIMRCULEXNT-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 = 50195889   

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 4 (Homo sapiens (Human))	BDBM50195889 (3-(pyridin-3-yl)-7-(3,4,5-trimethoxyphenyl)thieno[...) Show SMILES COc1cc(cc(OC)c1OC)-c1cnc(N)c2c(csc12)-c1cccnc1 Show InChI InChI=1S/C21H19N3O3S/c1-25-16-7-13(8-17(26-2)19(16)27-3)14-10-24-21(22)18-15(11-28-20(14)18)12-5-4-6-23-9-12/h4-11H,1-3H3,(H2,22,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline K.K. Curated by ChEMBL					Assay Description Inhibition of human EphB4 by scintillation proximity method				Bioorg Med Chem Lett 17: 250-4 (2006) Article DOI: 10.1016/j.bmcl.2006.09.050 BindingDB Entry DOI: 10.7270/Q2SB45D5
					More data for this Ligand-Target Pair