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• W2112811927 endingPage "1494" @default.
• W2112811927 startingPage "1483" @default.
• W2112811927 abstract "Abstract Recent biological and computational advances in drug design have led to renewed interest in targeted covalent inhibition as an efficient and practical approach for the development of new drugs. As part of our continuing efforts in the exploration of the therapeutic potential of resorcylic acid lactones (RALs), we report herein the design, synthesis, and biological evaluation of conveniently accessible RAL enamide analogues as novel covalent inhibitors of MAP kinase interacting kinases (MNKs). In this study, we have successfully demonstrated that the covalent binding ability of RAL enamides can be tuned by attaching an electron‐withdrawing motif, such as an acyl group, to enhance its reactivity toward the cysteine residues at the MNK1/2 binding sites. We have also shown that 1 H NMR spectroscopy is a convenient and effective tool for screening the covalent binding activities of enamides using cysteamine as a mimic of the key cysteine residue in the enzyme, whereas mass spectrometric analysis confirms covalent modification of the kinases. Preliminary optimization of the initial hit led to the discovery of enamides with low micromolar activity in MNK assays. Cancer cell line assays have identified RAL enamides that inhibit the growth of cancer cells with similar potency to the natural product L‐783 ,277." @default.
• W2112811927 created "2016-06-24" @default.
• W2112811927 creator A5002384844 @default.
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• W2112811927 date "2013-08-08" @default.
• W2112811927 modified "2023-10-10" @default.
• W2112811927 title "Rational Design of Resorcylic Acid Lactone Analogues as Covalent MNK1/2 Kinase Inhibitors by Tuning the Reactivity of an Enamide Michael Acceptor" @default.
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• W2112811927 doi "https://doi.org/10.1002/cmdc.201300231" @default.
• W2112811927 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23929665" @default.
• W2112811927 hasPublicationYear "2013" @default.
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