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Xenobiotica
the fate of foreign compounds in biological systems
Volume 10, 1980 - Issue 11
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Research Article

Epoxide-diol pathway of Δ1 -THC in the rat in vitro

Pages 805-809 | Received 25 Mar 1980, Published online: 22 Sep 2008
 

Abstract

1. 1α,2α-Epoxyhexahydrocannabinol was identified as a metabolite of Δ1-tetrahydrocannabinol.

2. The two trans-1,2-dihydroxyhexahydrocannabinol isomers, 1α,2β-dihydroxy-hexahydrocannabinol and 1β,2α-dihydroxyhexahydrocannabinol (as their acetates) were tentatively identified as metabolites from incubation of 1α,2α-epoxyhexahydrocannabinol with rat hepatic microsomes in vitro.

3. The 1α,2α-epoxyhexahydrocannabinol acetate was found to be a good substrate for epoxide hydratase as compared to styrene oxide.

4. The synthesis of metabolites of 1α,2α-epoxyhexahydrocannabinol is described.

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