BDBM13228 2-[[(tert-Butyloxy)carbonyl]-amino]-4-methyl-N-(2-methoxy-6-methylphenyl)-1,3-thiazole-5-carboxamide::BMS-354825 tert-Butoxycarbamate Analog 5i::CHEMBL132399::tert-butyl N-{5-[(2-methoxy-6-methylphenyl)carbamoyl]-4-methyl-1,3-thiazol-2-yl}carbamate

SMILES COc1cccc(C)c1NC(=O)c1sc(NC(=O)OC(C)(C)C)nc1C

InChI Key InChIKey=FUWPWSPNEHBSEJ-UHFFFAOYSA-N

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 13228   

TargetProto-oncogene tyrosine-protein kinase LCK(Mus musculus)
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM13228(2-[[(tert-Butyloxy)carbonyl]-amino]-4-methyl-N-(2-...)
Affinity DataIC50:  2.43E+4nMAssay Description:In vitro inhibition of murine Lck kinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase LCK(Mus musculus)
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM13228(2-[[(tert-Butyloxy)carbonyl]-amino]-4-methyl-N-(2-...)
Affinity DataIC50:  2.43E+4nMpH: 7.0 T: 2°CAssay Description:IC50 is the inhibitor concentration, which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-33P] lab...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed