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Chiral Alkyl Halides: Underexplored Motifs in Medicine

While alkyl halides are valuable intermediates in synthetic organic chemistry, their use as bioactive motifs in drug discovery and medicinal chemistry is rare in comparison. This is likely attributable to the common misconception that these compounds are merely non-specific alkylators in biological...

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Autores principales: Gál, Bálint, Bucher, Cyril, Burns, Noah Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128749/
https://www.ncbi.nlm.nih.gov/pubmed/27827902
http://dx.doi.org/10.3390/md14110206
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author Gál, Bálint
Bucher, Cyril
Burns, Noah Z.
author_facet Gál, Bálint
Bucher, Cyril
Burns, Noah Z.
author_sort Gál, Bálint
collection PubMed
description While alkyl halides are valuable intermediates in synthetic organic chemistry, their use as bioactive motifs in drug discovery and medicinal chemistry is rare in comparison. This is likely attributable to the common misconception that these compounds are merely non-specific alkylators in biological systems. A number of chlorinated compounds in the pharmaceutical and food industries, as well as a growing number of halogenated marine natural products showing unique bioactivity, illustrate the role that chiral alkyl halides can play in drug discovery. Through a series of case studies, we demonstrate in this review that these motifs can indeed be stable under physiological conditions, and that halogenation can enhance bioactivity through both steric and electronic effects. Our hope is that, by placing such compounds in the minds of the chemical community, they may gain more traction in drug discovery and inspire more synthetic chemists to develop methods for selective halogenation.
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spelling pubmed-51287492016-12-06 Chiral Alkyl Halides: Underexplored Motifs in Medicine Gál, Bálint Bucher, Cyril Burns, Noah Z. Mar Drugs Review While alkyl halides are valuable intermediates in synthetic organic chemistry, their use as bioactive motifs in drug discovery and medicinal chemistry is rare in comparison. This is likely attributable to the common misconception that these compounds are merely non-specific alkylators in biological systems. A number of chlorinated compounds in the pharmaceutical and food industries, as well as a growing number of halogenated marine natural products showing unique bioactivity, illustrate the role that chiral alkyl halides can play in drug discovery. Through a series of case studies, we demonstrate in this review that these motifs can indeed be stable under physiological conditions, and that halogenation can enhance bioactivity through both steric and electronic effects. Our hope is that, by placing such compounds in the minds of the chemical community, they may gain more traction in drug discovery and inspire more synthetic chemists to develop methods for selective halogenation. MDPI 2016-11-04 /pmc/articles/PMC5128749/ /pubmed/27827902 http://dx.doi.org/10.3390/md14110206 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Gál, Bálint
Bucher, Cyril
Burns, Noah Z.
Chiral Alkyl Halides: Underexplored Motifs in Medicine
title Chiral Alkyl Halides: Underexplored Motifs in Medicine
title_full Chiral Alkyl Halides: Underexplored Motifs in Medicine
title_fullStr Chiral Alkyl Halides: Underexplored Motifs in Medicine
title_full_unstemmed Chiral Alkyl Halides: Underexplored Motifs in Medicine
title_short Chiral Alkyl Halides: Underexplored Motifs in Medicine
title_sort chiral alkyl halides: underexplored motifs in medicine
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128749/
https://www.ncbi.nlm.nih.gov/pubmed/27827902
http://dx.doi.org/10.3390/md14110206
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