BDBM50112947 (6,7-Dimethoxy-imidazo[1,5-a]quinoxalin-4-yl)-(2,6-dimethyl-phenyl)-amine::CHEMBL281035::N-(2,6-dimethylphenyl)-6,7-dimethoxyimidazo[1,5-a]quinoxalin-4-amine

SMILES: COc1ccc2c(nc(Nc3c(C)cccc3C)c3cncn23)c1OC

InChI Key: InChIKey=IPHIFOKYAREGSF-UHFFFAOYSA-N

Data: 3 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 3 hits for monomerid = 50112947   

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
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50112947 ((6,7-Dimethoxy-imidazo[1,5-a]quinoxalin-4-yl)-(2,6...) Show SMILES COc1ccc2c(nc(Nc3c(C)cccc3C)c3cncn23)c1OC Show InChI InChI=1S/C20H20N4O2/c1-12-6-5-7-13(2)17(12)22-20-15-10-21-11-24(15)14-8-9-16(25-3)19(26-4)18(14)23-20/h5-11H,1-4H3,(H,22,23)	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.40	n/a	n/a	n/a	n/a	n/a	n/a
Bristol Myers Squibb Pharmaceutical Research Institute Curated by ChEMBL					Assay Description Inhibitory activity against recombinant p56 Lck tyrosine kinase expressed as a His-tagged protein in insect cells using a baculovirus expression syst...				Bioorg Med Chem Lett 12: 1361-4 (2002) BindingDB Entry DOI: 10.7270/Q2R78DJ1
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50112947 ((6,7-Dimethoxy-imidazo[1,5-a]quinoxalin-4-yl)-(2,6...) Show SMILES COc1ccc2c(nc(Nc3c(C)cccc3C)c3cncn23)c1OC Show InChI InChI=1S/C20H20N4O2/c1-12-6-5-7-13(2)17(12)22-20-15-10-21-11-24(15)14-8-9-16(25-3)19(26-4)18(14)23-20/h5-11H,1-4H3,(H,22,23)	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.40	n/a	n/a	n/a	n/a	n/a	n/a
University of Zurich Curated by ChEMBL					Assay Description Inhibition of Lck				J Med Chem 51: 1179-88 (2008) Article DOI: 10.1021/jm070654j BindingDB Entry DOI: 10.7270/Q29Z95RD
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50112947 ((6,7-Dimethoxy-imidazo[1,5-a]quinoxalin-4-yl)-(2,6...) Show SMILES COc1ccc2c(nc(Nc3c(C)cccc3C)c3cncn23)c1OC Show InChI InChI=1S/C20H20N4O2/c1-12-6-5-7-13(2)17(12)22-20-15-10-21-11-24(15)14-8-9-16(25-3)19(26-4)18(14)23-20/h5-11H,1-4H3,(H,22,23)	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.40	n/a	n/a	n/a	n/a	n/a	n/a
Yale University Curated by ChEMBL					Assay Description Evaluated for inhibition of human p56 Lck tyrosine kinase				J Med Chem 47: 2534-49 (2004) Article DOI: 10.1021/jm0304358 BindingDB Entry DOI: 10.7270/Q2KH0P3P
					More data for this Ligand-Target Pair