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Compile Data Set for Download or QSAR

Found 1 hit Enz. Inhib. hit(s) with Target = 'Src' and Monomerid = 3923   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM3923
PNG
(4-[(1-phenyl-1H-1,3-benzodiazol-5-yl)oxy]butan-1-o...)
Show SMILES OCCCCOc1ccc2n(cnc2c1)-c1ccccc1
Show InChI InChI=1S/C17H18N2O2/c20-10-4-5-11-21-15-8-9-17-16(12-15)18-13-19(17)14-6-2-1-3-7-14/h1-3,6-9,12-13,20H,4-5,10-11H2
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 2.50E+4n/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 42: 2373-82 (1999)


Article DOI: 10.1021/jm980658b
BindingDB Entry DOI: 10.7270/Q2W957B2
More data for this
Ligand-Target Pair