BDBM50196874 CHEMBL3907638

SMILES: Cl.COc1ccc(C(=O)CC(C)C)c(OC[C@@H](O)CNC(C)(C)C)c1

InChI Key: InChIKey=JDRJOKWNZIOFIT-UQKRIMTDSA-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 = 50196874   

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
Neuronal proto-oncogene tyrosine-protein kinase Src (Mus musculus (Mouse))	BDBM50196874 (CHEMBL3907638) Show SMILES Cl.COc1ccc(C(=O)CC(C)C)c(OC[C@@H](O)CNC(C)(C)C)c1 |r| Show InChI InChI=1S/C19H31NO4.ClH/c1-13(2)9-17(22)16-8-7-15(23-6)10-18(16)24-12-14(21)11-20-19(3,4)5;/h7-8,10,13-14,20-21H,9,11-12H2,1-6H3;1H/t14-;/m0./s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.38E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Medical Sciences and Peking Union Medical College Curated by ChEMBL					Assay Description Inhibition of Src in mouse BV2 cells assessed as suppression of LPS-induced NO release preincubated for 1 hr followed by LPS addition measured after ...				J Med Chem 59: 9062-9079 (2016) Article DOI: 10.1021/acs.jmedchem.6b00976 BindingDB Entry DOI: 10.7270/Q2B56MP4
					More data for this Ligand-Target Pair