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BDBM13257 BMS-354825 2-Heteroarylamino-thiazole Analog 12b::CHEMBL189675::N-(2-Chloro-6-methylphenyl)-2-[(3-pyridinyl)amino]-1,3-thiazole-5-carboxamide::N-(2-chloro-6-methylphenyl)-2-(pyridin-3-ylamino)-1,3-thiazole-5-carboxamide

SMILES: Cc1cccc(Cl)c1NC(=O)c1cnc(Nc2cccnc2)s1

InChI Key: InChIKey=WCBCZRZYPOPLAQ-UHFFFAOYSA-N

Data: 1 IC50

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   Substructure
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 13257   
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))
BDBM13257
PNG
(BMS-354825 2-Heteroarylamino-thiazole Analog 12b |...)
Show SMILES Cc1cccc(Cl)c1NC(=O)c1cnc(Nc2cccnc2)s1
Show InChI InChI=1S/C16H13ClN4OS/c1-10-4-2-6-12(17)14(10)21-15(22)13-9-19-16(23-13)20-11-5-3-7-18-8-11/h2-9H,1H3,(H,19,20)(H,21,22)
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

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CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 6.70n/an/an/an/an/an/a



Bristol-Myers Squibb Company



Assay Description
IC50 is the inhibitor concentration, which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-33P] lab...


J Med Chem 49: 6819-32 (2006)


Article DOI: 10.1021/jm060727j
BindingDB Entry DOI: 10.7270/Q2QN6501
More data for this
Ligand-Target Pair