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Design, synthesis and conformational analysis of oligobenzanilides as multi-facial alpha-helix mimetics
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acs.orglett.9b01115.pdf | Published version | 2.07 MB | Adobe PDF | View/Open |
Title: | Design, synthesis and conformational analysis of oligobenzanilides as multi-facial alpha-helix mimetics |
Authors: | Flack, T Romain, C White, A Haycock, P Barnard, A |
Item Type: | Journal Article |
Abstract: | The design, synthesis, and conformational analysis of an oligobenzanilide helix mimetic scaffold capable of simultaneous mimicry of two faces of an α-helix is reported. The synthetic methodology provides access to diverse monomer building blocks amenable to solid-phase assembly in just four synthetic steps. The conformational flexibility of model dimers was investigated using a combination of solid and solution state methodologies supplemented with DFT calculations. The lack of noncovalent constraints allows for significant conformational plasticity in the scaffold, thus permitting it to successfully mimic residues i, i+2, i+4, i+6, i +7, and i+9 of a canonical α-helix. |
Issue Date: | 21-Jun-2019 |
Date of Acceptance: | 1-Jun-2019 |
URI: | http://hdl.handle.net/10044/1/71702 |
DOI: | https://dx.doi.org/10.1021/acs.orglett.9b01115 |
ISSN: | 1523-7052 |
Publisher: | American Chemical Society |
Start Page: | 4433 |
End Page: | 4438 |
Journal / Book Title: | Organic Letters |
Volume: | 21 |
Issue: | 12 |
Copyright Statement: | © 2019 American Chemical Society. This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
Sponsor/Funder: | Wellcome Trust |
Funder's Grant Number: | 105603/Z/14/Z |
Keywords: | Science & Technology Physical Sciences Chemistry, Organic Chemistry PROTEIN-PROTEIN INTERACTIONS EXPLORING KEY ORIENTATIONS SMALL-MOLECULE INHIBITORS ROTATION INTERFACES AMIDE 03 Chemical Sciences Organic Chemistry |
Publication Status: | Published |
Online Publication Date: | 2019-06-12 |
Appears in Collections: | Chemistry Biological and Biophysical Chemistry |