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BDBM50112952 4-(2,6-Dimethyl-phenyl)-imidazo[1,5-a]quinoxaline::4-(2,6-dimethylphenyl)imidazo[1,5-a]quinoxaline::CHEMBL30250

SMILES: Cc1cccc(C)c1-c1nc2ccccc2n2cncc12

InChI Key: InChIKey=ZPRRIUIBOLATFJ-UHFFFAOYSA-N

Data: 2 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 2 hits for monomerid = 50112952   
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
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50112952
PNG
(4-(2,6-Dimethyl-phenyl)-imidazo[1,5-a]quinoxaline ...)
Show SMILES Cc1cccc(C)c1-c1nc2ccccc2n2cncc12 |(10.14,-7.28,;11.48,-6.52,;12.82,-7.3,;14.17,-6.53,;14.17,-4.97,;12.84,-4.19,;12.84,-2.66,;11.49,-4.97,;10.16,-4.18,;8.81,-4.95,;7.49,-4.18,;6.16,-4.95,;4.83,-4.18,;4.83,-2.64,;6.16,-1.87,;7.49,-2.64,;8.81,-1.87,;9.14,-.37,;10.67,-.22,;11.31,-1.61,;10.16,-2.64,)|
Show InChI InChI=1S/C18H15N3/c1-12-6-5-7-13(2)17(12)18-16-10-19-11-21(16)15-9-4-3-8-14(15)20-18/h3-11H,1-2H3
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents

Article
PubMed
n/an/a>1.25E+4n/an/an/an/an/an/a



University of Zurich

Curated by ChEMBL


Assay Description
Inhibition of Lck


J Med Chem 51: 1179-88 (2008)


Article DOI: 10.1021/jm070654j
BindingDB Entry DOI: 10.7270/Q29Z95RD
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50112952
PNG
(4-(2,6-Dimethyl-phenyl)-imidazo[1,5-a]quinoxaline ...)
Show SMILES Cc1cccc(C)c1-c1nc2ccccc2n2cncc12 |(10.14,-7.28,;11.48,-6.52,;12.82,-7.3,;14.17,-6.53,;14.17,-4.97,;12.84,-4.19,;12.84,-2.66,;11.49,-4.97,;10.16,-4.18,;8.81,-4.95,;7.49,-4.18,;6.16,-4.95,;4.83,-4.18,;4.83,-2.64,;6.16,-1.87,;7.49,-2.64,;8.81,-1.87,;9.14,-.37,;10.67,-.22,;11.31,-1.61,;10.16,-2.64,)|
Show InChI InChI=1S/C18H15N3/c1-12-6-5-7-13(2)17(12)18-16-10-19-11-21(16)15-9-4-3-8-14(15)20-18/h3-11H,1-2H3
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents

PubMed
n/an/a>1.25E+4n/an/an/an/an/an/a



Bristol Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL


Assay Description
Inhibitory activity against recombinant p56 Lck tyrosine kinase expressed as a His-tagged protein in insect cells using a baculovirus expression syst...


Bioorg Med Chem Lett 12: 1361-4 (2002)


BindingDB Entry DOI: 10.7270/Q2R78DJ1
More data for this
Ligand-Target Pair