Design, synthesis, and structure-activity relationship studies of thiophene-3-carboxamide derivatives as dual inhibitors of the c-Jun N-terminal kinase.
Bioorg Med Chem, 2011/4/15;19(8):2582-8.
De SK[1], Barile E, Chen V, Stebbins JL, Cellitti JF, Machleidt T, Carlson CB, Yang L, Dahl R, Pellecchia M
Affiliations
PMID: 21458276DOI: 10.1016/j.bmc.2011.03.017
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Abstract
We report comprehensive structure-activity relationship studies on a novel series of c-Jun N-terminal kinase (JNK) inhibitors. Intriguingly, the compounds have a dual inhibitory activity by functioning as both ATP and JIP mimetics, possibly by binding to both the ATP binding site and to the docking site of the kinase. Several of such novel compounds display potent JNK inhibitory profiles both in vitro and in cell.
MeSH terms
Adenosine Triphosphate; Binding Sites; Cell Line; Drug Design; Humans; JNK Mitogen-Activated Protein Kinases; Molecular Mimicry; Protein Binding; Protein Kinase Inhibitors; Structure-Activity Relationship; Thiophenes
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