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

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 = 13228   

Target/Host (Institution)	Ligand	Target/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	pH	Temp °C
Tyrosine-protein kinase LCK (Mus musculus)	BDBM13228 (2-[[(tert-Butyloxy)carbonyl]-amino]-4-methyl-N-(2-...) Show SMILES COc1cccc(C)c1NC(=O)c1sc(NC(=O)OC(C)(C)C)nc1C Show InChI InChI=1S/C18H23N3O4S/c1-10-8-7-9-12(24-6)13(10)20-15(22)14-11(2)19-16(26-14)21-17(23)25-18(3,4)5/h7-9H,1-6H3,(H,20,22)(H,19,21,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	2.43E+4	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Pharmaceutical Research Institute Curated by ChEMBL					Assay Description In vitro inhibition of murine Lck kinase.				Bioorg Med Chem Lett 13: 4007-10 (2003) BindingDB Entry DOI: 10.7270/Q2CC103J
					More data for this Ligand-Target Pair
Lck (Mus musculus)	BDBM13228 (2-[[(tert-Butyloxy)carbonyl]-amino]-4-methyl-N-(2-...) Show SMILES COc1cccc(C)c1NC(=O)c1sc(NC(=O)OC(C)(C)C)nc1C Show InChI InChI=1S/C18H23N3O4S/c1-10-8-7-9-12(24-6)13(10)20-15(22)14-11(2)19-16(26-14)21-17(23)25-18(3,4)5/h7-9H,1-6H3,(H,20,22)(H,19,21,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.43E+4	n/a	n/a	n/a	n/a	7.0	22
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