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BDBM3597 (4Z)-4-[(3-bromophenyl)imino]-N,3-dimethyl-3H,4H-pyrido[4,3-d]pyrimidin-7-amine::N4-(3-bromophenyl)-3-methyl-7-(methylamino)-pyrido[4,3-d]pyrimidin-4(3H)-imine::Pyrido[4,3-d]pyrimidine 12

SMILES: CNc1cc2ncn(C)\c(=N/c3cccc(Br)c3)c2cn1

InChI Key: InChIKey=KGPJHDOZKFVFLW-HKWRFOASSA-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 = 3597   
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))
BDBM3597
PNG
((4Z)-4-[(3-bromophenyl)imino]-N,3-dimethyl-3H,4H-p...)
Show SMILES CNc1cc2ncn(C)\c(=N/c3cccc(Br)c3)c2cn1
Show InChI InChI=1S/C15H14BrN5/c1-17-14-7-13-12(8-18-14)15(21(2)9-19-13)20-11-5-3-4-10(16)6-11/h3-9H,1-2H3,(H,17,18)/b20-15-
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 3.10n/an/an/an/a7.422



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 39: 1823-35 (1996)


Article DOI: 10.1021/jm9508651
BindingDB Entry DOI: 10.7270/Q2X928GF
More data for this
Ligand-Target Pair