Cargando…
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...
Autores principales: | , , |
---|---|
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 |
_version_ | 1782470464812089344 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5128749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT galbalint chiralalkylhalidesunderexploredmotifsinmedicine AT buchercyril chiralalkylhalidesunderexploredmotifsinmedicine AT burnsnoahz chiralalkylhalidesunderexploredmotifsinmedicine |