

Publisher: John Wiley & Sons Inc
E-ISSN: 1860-7187|10|12|2116-2116
ISSN: 1860-7179
Source: CHEMMEDCHEM, Vol.10, Iss.12, 2015-12, pp. : 2116-2116
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Abstract
The back cover picture shows our modular approach in reassembling previously described building blocks of inhibitors for the mitogen‐activated protein kinase kinase (MEK). We have combined our recently identified C6‐phenoxy side chains with cores derived from two MEK inhibitors that are currently in clinical development. This modular approach has allowed us to synthesize and characterize two novel series of highly potent allosteric MEK inhibitors. We report their pharmacokinetic properties and in vivo efficacy data for one advanced preclinical candidate. Inspection of effects of these new inhibitors on MEK phosphorylation allowed us to further unravel structural intricacies of MEK–Raf feedback interactions. More details can be found in the Full Paper by Ingo V. Hartung, Marion Hitchcock et al. on page 2004 in Issue 12, 2015 (DOI: 10.1002/cmdc.201500442).
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