Towards more drug-like proteomimetics: two-faced, synthetic α-helix mimetics based on a purine scaffold
M E Lanning1, P T Wilder, H Bailey
1Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, 20 N. Pine St., Baltimore, MD 21201, USA. sfletcher@rx.umaryland.edu.
Organic & Biomolecular Chemistry
|July 25, 2015
Abstract:
Mimicry of two faces of an α-helix might yield more potent and more selective inhibitors of aberrant, helix-mediated protein-protein interactions (PPI). Herein, we demonstrate that a 2,6,9-tri-substituted purine is capable of disrupting the Mcl-1-Bak-BH3 PPI through effective mimicry of key residues on opposing faces of the Bak-BH3 α-helix.
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