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Design, Synthesis, and Conformational Analysis of Oligobenzanilides as Multifacial α-Helix Mimetics

[Image: see text] 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...

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Autores principales: Flack, Theo, Romain, Charles, White, Andrew J. P., Haycock, Peter R., Barnard, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593395/
https://www.ncbi.nlm.nih.gov/pubmed/31188616
http://dx.doi.org/10.1021/acs.orglett.9b01115
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author Flack, Theo
Romain, Charles
White, Andrew J. P.
Haycock, Peter R.
Barnard, Anna
author_facet Flack, Theo
Romain, Charles
White, Andrew J. P.
Haycock, Peter R.
Barnard, Anna
author_sort Flack, Theo
collection PubMed
description [Image: see text] 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.
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spelling pubmed-65933952019-10-30 Design, Synthesis, and Conformational Analysis of Oligobenzanilides as Multifacial α-Helix Mimetics Flack, Theo Romain, Charles White, Andrew J. P. Haycock, Peter R. Barnard, Anna Org Lett [Image: see text] 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. American Chemical Society 2019-06-12 2019-06-21 /pmc/articles/PMC6593395/ /pubmed/31188616 http://dx.doi.org/10.1021/acs.orglett.9b01115 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Flack, Theo
Romain, Charles
White, Andrew J. P.
Haycock, Peter R.
Barnard, Anna
Design, Synthesis, and Conformational Analysis of Oligobenzanilides as Multifacial α-Helix Mimetics
title Design, Synthesis, and Conformational Analysis of Oligobenzanilides as Multifacial α-Helix Mimetics
title_full Design, Synthesis, and Conformational Analysis of Oligobenzanilides as Multifacial α-Helix Mimetics
title_fullStr Design, Synthesis, and Conformational Analysis of Oligobenzanilides as Multifacial α-Helix Mimetics
title_full_unstemmed Design, Synthesis, and Conformational Analysis of Oligobenzanilides as Multifacial α-Helix Mimetics
title_short Design, Synthesis, and Conformational Analysis of Oligobenzanilides as Multifacial α-Helix Mimetics
title_sort design, synthesis, and conformational analysis of oligobenzanilides as multifacial α-helix mimetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593395/
https://www.ncbi.nlm.nih.gov/pubmed/31188616
http://dx.doi.org/10.1021/acs.orglett.9b01115
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