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Amphipathic α-helix mimetics based on a 1,2-diphenylacetylene scaffold
Kwan-Young Jung1, Kenno Vanommeslaeghe, Maryanna E Lanning
1Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, 20 North Pine Street, Baltimore, Maryland 21201, USA.
Abstract:
In order to mimic amphipathic α-helices, a novel scaffold based on a 1,2-diphenylacetylene was designed. NMR and computational modeling confirmed that an intramolecular hydrogen bond favors conformations of the 1,2-diphenylacetylene that allow for accurate mimicry of the i, i + 7 and i + 2, i + 5 side chains found on opposing faces of an α-helix.
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