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BDBM3675 7-N-[4-(dimethylamino)butyl]-4-N-(3-methylphenyl)pyrido[4,3-d]pyrimidine-4,7-diamine::7-[[4-(Dimethylamino)butyl]amino]-4-[(3-methylphenyl)amino]pyrido[4,3-d]pyrimidine::pyrido[4,3-d]pyrimidine deriv. 4n

SMILES: CN(C)CCCCNc1cc2ncnc(Nc3cccc(C)c3)c2cn1

InChI Key: InChIKey=ANAQVLGHFOBDLP-UHFFFAOYSA-N

Data: 1 IC50

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   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 3675   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM3675
PNG
(7-N-[4-(dimethylamino)butyl]-4-N-(3-methylphenyl)p...)
Show SMILES CN(C)CCCCNc1cc2ncnc(Nc3cccc(C)c3)c2cn1
Show InChI InChI=1S/C20H26N6/c1-15-7-6-8-16(11-15)25-20-17-13-22-19(12-18(17)23-14-24-20)21-9-4-5-10-26(2)3/h6-8,11-14H,4-5,9-10H2,1-3H3,(H,21,22)(H,23,24,25)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 5.40n/an/an/an/an/an/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