Natural cannabinoids: templates for drug discovery

Life Sci. 2005 Dec 22;78(5):454-66. doi: 10.1016/j.lfs.2005.09.014. Epub 2005 Oct 19.

Abstract

Recent studies have elucidated the biosynthetic pathway of cannabinoids and have highlighted the preference for a C-3 n-pentyl side chain in the most prominently represented cannabinoids from Cannabis sativa and their medicinally important decarboxylation products. The corresponding C-3 n-propyl side chain containing cannabinoids are also found, although in lesser quantities. Structure-activity relationship (SAR) studies performed on Delta(9)-tetrahydrocannabinol (Delta(9)-THC), the key psychoactive ingredient of Cannabis, and its synthetic analogues have identified the C-3 side chain as the key pharmacophore for ligand affinity and selectivity for the known cannabinoid receptors and for pharmacological potency. Interestingly, the terminal n-pentyl saturated hydrocarbon side chain of endocannabinoids also plays a corresponding crucial role in conferring similar properties. This review briefly summarizes the biosynthesis of cannabinoids and endocannabinoids and focuses on their side chain SAR.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Cannabinoid Receptor Modulators / biosynthesis
  • Cannabinoid Receptor Modulators / chemistry
  • Cannabinoid Receptor Modulators / pharmacology
  • Cannabinoids / biosynthesis
  • Cannabinoids / chemistry*
  • Cannabinoids / pharmacology*
  • Humans
  • Molecular Conformation
  • Pharmacology*
  • Structure-Activity Relationship

Substances

  • Cannabinoid Receptor Modulators
  • Cannabinoids