4.7 Review

Chiral Alkyl Halides: Underexplored Motifs in Medicine

Journal

MARINE DRUGS
Volume 14, Issue 11, Pages -

Publisher

MDPI AG
DOI: 10.3390/md14110206

Keywords

alkyl halide; stereochemistry; lipophilicity; anesthetic; clindamycin; corticosteroid; pimecrolimus; sucralose; halomon; lapachone; astins; forazoline

Funding

  1. Stanford University
  2. National Institutes of Health [R01 GM114061]

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available