Stereochemical effects of 11-OH-delta 8-THC-dimethylheptyl in mice and dogs

Pharmacol Biochem Behav. 1989 Mar;32(3):661-6. doi: 10.1016/0091-3057(89)90014-2.

Abstract

The effects of the enantiomers of 11-hydroxy-delta 8-tetrahydrocannabinol-dimethylheptyl (11-OH-delta 8-THC-DMH) on spontaneous activity, rectal temperature, tail-flick latency, and catalepsy were studied in mice and in the dog static-ataxia model to determine the relative potency of each enantiomer. The (-)-enantiomer was active in all tests between 3-100 micrograms/kg, while the (+)-enantiomer was inactive at 30 mg/kg in the mouse and 1 mg/kg in the dog. The (-)-enantiomer was 100-800 times more potent than delta 9-THC in the mouse. The high degree of enantioselectivity and potency are suggestive of an interaction at a specific site such as a receptor.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Body Temperature Regulation / drug effects
  • Catalepsy / chemically induced*
  • Dogs
  • Dronabinol / analogs & derivatives*
  • Dronabinol / pharmacology
  • Male
  • Mice
  • Mice, Inbred ICR
  • Motor Activity / drug effects*
  • Reaction Time / drug effects
  • Stereoisomerism

Substances

  • 11-hydroxy-delta(8)-tetrahydrocannabinol
  • Dronabinol