BDBM3658 4-N-(3-bromophenyl)-7-N-[2-(dimethylamino)ethyl]-7-N-methylpyrido[4,3-d]pyrimidine-4,7-diamine::4-[(3-Bromophenyl)amino]-7-[N-[2-(dimethylamino)-ethyl]-N-methylamino]pyrido[4,3-d]pyrimidine::pyrido[4,3-d]pyrimidine deriv. 3p

SMILES: CN(C)CCN(C)c1cc2ncnc(Nc3cccc(Br)c3)c2cn1

InChI Key: InChIKey=SXQLAYKKOJLZRB-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 = 3658   

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
Epidermal growth factor receptor (Homo sapiens (Human))	BDBM3658 (4-N-(3-bromophenyl)-7-N-[2-(dimethylamino)ethyl]-7...) Show SMILES CN(C)CCN(C)c1cc2ncnc(Nc3cccc(Br)c3)c2cn1 Show InChI InChI=1S/C18H21BrN6/c1-24(2)7-8-25(3)17-10-16-15(11-20-17)18(22-12-21-16)23-14-6-4-5-13(19)9-14/h4-6,9-12H,7-8H2,1-3H3,(H,21,22,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	40	n/a	n/a	n/a	n/a	7.4	25
University of Auckland					Assay Description IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...				J Med Chem 40: 3915-25 (1997) Article DOI: 10.1021/jm970366v BindingDB Entry DOI: 10.7270/Q2NS0S2V
					More data for this Ligand-Target Pair