BDBM3678 7-N-[3-(1H-imidazol-1-yl)propyl]-4-N-(3-methylphenyl)pyrido[4,3-d]pyrimidine-4,7-diamine::7-[[3-(Imidazol-1-yl)propyl]amino]-4-[(3-methylphenyl)amino]pyrido[4,3-d]pyrimidine::pyrido[4,3-d]pyrimidine deriv. 4y

SMILES: Cc1cccc(Nc2ncnc3cc(NCCCn4ccnc4)ncc23)c1

InChI Key: InChIKey=OKJBKEUQKDDCKF-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 = 3678   

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))	BDBM3678 (7-N-[3-(1H-imidazol-1-yl)propyl]-4-N-(3-methylphen...) Show SMILES Cc1cccc(Nc2ncnc3cc(NCCCn4ccnc4)ncc23)c1 Show InChI InChI=1S/C20H21N7/c1-15-4-2-5-16(10-15)26-20-17-12-23-19(11-18(17)24-13-25-20)22-6-3-8-27-9-7-21-14-27/h2,4-5,7,9-14H,3,6,8H2,1H3,(H,22,23)(H,24,25,26)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.5	n/a	n/a	n/a	n/a	n/a	n/a
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