Journal
ACS CHEMICAL NEUROSCIENCE
Volume 11, Issue 21, Pages 3672-3682Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acschemneuro.0c00591
Keywords
Cannabinoid; pharmacology; CUMYL; PICA; CHMICA; FUBICA
Funding
- NHMRC [1161571]
- Brain and Mind Centre Research Development Grant from The University of Sydney
- Lambert Initiative for Cannabinoid Therapeutics
- University of Sydney
- National Health and Medical Research Council of Australia [1161571] Funding Source: NHMRC
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Synthetic cannabinoid receptor agonists (SCRAs) represent the most rapidly expanding class of new psychoactive substances (NPSs). Despite the prevalence and potency of recent chiral indole-3-carboxamide SCRAs, few pharmacological data are available regarding the enantiomeric bias of these NPSs toward human CB1 and CB2 receptors. A series of homochiral indole-3-carboxamides derived from (S)- and (R)-alpha-methylbenzylamine and featuring variation of the 1-alkyl substituent were prepared, pharmacologically evaluated, and compared to related achiral congeners derived from cumyl- and benzylamine. Competitive binding assays demonstrated that all analogues derived from either enantiomer of alpha-methylbenzylamine (14-17) showed affinities for CB1 (K-i = 47.9-813 nM) and CB2 (K-i = 47.9-347 nM) that were intermediate to that of the corresponding benzylic (10-13, CB1 K-i = 550 nM to >10 mu M; CB2 K-i = 61.7 nM to >10 mu M) and cumyl derivatives (6-9, CB1 K-i = 12.6-21.4 nM; CB2 K-i = 2.95-24.5 nM). In a fluorometric membrane potential assay, all alpha-methylbenzyl analogues (excluding 17) were potent, efficacious agonists of CB1 (EC50 = 32-464 nM; E-max = 89-104%) and low efficacy agonists of CB2 (EC50 = 54-500 nM; E-max = 52-77%), with comparable or greater potency than the benzyl analogues and much lower potency than the cumyl derivatives, consistent with binding trends. The relatively greater affinity and potency of (S)-14-17 compared to (R)-14-17 analogues at CB1 highlighted an enantiomeric bias for this series of SCRAs. Molecular dynamics simulations provided a conformational basis for the observed differences in agonist potency at CB1 pending benzylic substitution.
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