Bioorganic & Medicinal Chemistry Letters 2007-05-15

Novel bis(indolyl)maleimide pyridinophanes that are potent, selective inhibitors of glycogen synthase kinase-3.

Han-Cheng Zhang, Llorente V R Boñaga, Hong Ye, Claudia K Derian, Bruce P Damiano, Bruce E Maryanoff

文献索引：Bioorg. Med. Chem. Lett. 17(10) , 2863-8, (2007)

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摘要

Novel bis(indolyl)maleimide pyridinophanes 3, 9a, 9b, 10a, 10b, and 11 were prepared by cobalt-mediated [2+2+2] cycloaddition of an appropriate alpha,omega-diyne with an N,N-dialkylcyanamide. These macrocyclic heterophanes were found to be potent, selective inhibitors of glycogen synthase kinase-3beta. An X-ray structure of a co-crystal of GSK-3beta and 3 (IC(50)=3nM) depicts the hydrogen bonding and hydrophobic interactions in the ATP-binding pocket of this serine/threonine protein kinase.