BDBM50185658 CHEMBL3822690

SMILES: COc1cc(\C=C/C(=O)OCCc2ccc(OC)c(OC)c2)cc(OC)c1O

InChI Key: InChIKey=MNCNATMJPXYRTH-VURMDHGXSA-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 = 50185658   

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
Hepatocyte growth factor receptor (Homo sapiens (Human))	BDBM50185658 (CHEMBL3822690) Show SMILES COc1cc(\C=C/C(=O)OCCc2ccc(OC)c(OC)c2)cc(OC)c1O Show InChI InChI=1S/C21H24O7/c1-24-16-7-5-14(11-17(16)25-2)9-10-28-20(22)8-6-15-12-18(26-3)21(23)19(13-15)27-4/h5-8,11-13,23H,9-10H2,1-4H3/b8-6-	PDB MMDB KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Louisiana at Monroe Curated by ChEMBL					Assay Description Inhibition of recombinant human N-terminal His-tagged cytoplasmic c-MET kinase domain (956 to 1390 residues) phosphorylation expressed in baculovirus...				Eur J Med Chem 118: 299-315 (2016) BindingDB Entry DOI: 10.7270/Q2GT5Q35
					More data for this Ligand-Target Pair