%0 Journal Article
%T The Structure¨CFunction Relationships of Classical Cannabinoids: CB1/CB2 Modulation
%A Eric W. Bow
%A John M. Rimoldi
%J Archive of "Perspectives in Medicinal Chemistry".
%D 2016
%R 10.4137/PMC.S32171
%X The cannabinoids are members of a deceptively simple class of terpenophenolic secondary metabolites isolated from Cannabis sativa highlighted by (£¿)-¦¤9-tetrahydrocannabinol (THC), eliciting distinct pharmacological effects mediated largely by cannabinoid receptor (CB1 or CB2) signaling. Since the initial discovery of THC and related cannabinoids, synthetic and semisynthetic classical cannabinoid analogs have been evaluated to help define receptor binding modes and structure¨CCB1/CB2 functional activity relationships. This perspective will examine the classical cannabinoids, with particular emphasis on the structure¨Cactivity relationship of five regions: C3 side chain, phenolic hydroxyl, aromatic A-ring, pyran B-ring, and cyclohexenyl C-ring. Cumulative structure¨Cactivity relationship studies to date have helped define the critical structural elements required for potency and selectivity toward CB1 and CB2 and, more importantly, ushered the discovery and development of contemporary nonclassical cannabinoid modulators with enhanced physicochemical and pharmacological profiles
%K classical cannabinoids
%K phytocannabinoids
%K cannabidiol
%K tetrahydrocannabinol
%K Cannabis sativa
%U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4927043/