Steven T Staben, Nicole Blaquiere, Vickie Tsui, Aleksandr Kolesnikov, Steven Do, Erin K Bradley, Jenna Dotson, Richard Goldsmith, Timothy P Heffron, John Lesnick, Cristina Lewis, Jeremy Murray, Jim Nonomiya, Alan G Olivero, Jodie Pang, Lionel Rouge, Laurent Salphati, BinQing Wei, Christian Wiesmann, Ping Wu
Discovery Chemistry, Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USA. stevents@gene.com
Bioorganic & medicinal chemistry letters 2013 Feb 1Substructural class effects surrounding replacement of a 'cis' N-methyl aniline amide within potent and selective thienobenzoxepin PI3-kinase inhibitors are disclosed. While a simple aryl to alkyl switch was not tolerated due to differences in preferred amide conformation, heterocyclic amide isosteres with maintained aryl substitution improved potency and metabolic stability at the cost of physical properties. These gains in potency allowed lipophilic deconstruction of the arene to simple branched alkyl substituents. As such, overall lipophilicity-neutral, MW decreases were realized relative to the aniline amide series. The improved properties for lead compound 21 resulted in high permeability, solubility and bioavailability. Copyright © 2012 Elsevier Ltd. All rights reserved.
Steven T Staben, Nicole Blaquiere, Vickie Tsui, Aleksandr Kolesnikov, Steven Do, Erin K Bradley, Jenna Dotson, Richard Goldsmith, Timothy P Heffron, John Lesnick, Cristina Lewis, Jeremy Murray, Jim Nonomiya, Alan G Olivero, Jodie Pang, Lionel Rouge, Laurent Salphati, BinQing Wei, Christian Wiesmann, Ping Wu. Cis-amide isosteric replacement in thienobenzoxepin inhibitors of PI3-kinase. Bioorganic & medicinal chemistry letters. 2013 Feb 1;23(3):897-901
PMID: 23265894
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