Literature DB >> 6714

Identification of monohydroxylated metabolites of cannabidiol formed by rat liver.

B Martin, M Nordqvist, S Agurell, J E Lindgren, K Leander, M Binder.   

Abstract

Cannabidiol (CBD) was metabolized in vitro by rat liver enzymes. Unchanged CBD and eight monohydroxylated metabolites were isolated and positively identified. As previously reported, 7-hydroxy-CBD was the major metabolite. The second most abundant metabolite was 6alpha-hydroxy-CBD; whereas only a trace amount of 6beta-hydroxy-CBD was found. In addition hydroxylation occurred in all positions of the pentyl side chain, 4 inches-hydroxy-CBD being most abundant. 3 inches-Hydroxy-CBD was formed in half of the yield of 4 inches-hydroxy-CBD, while 1 inches-, 2 inches-, 5 inches-hydroxy-CBD were each formed in approximately one fourth of the yield of 4 inches-hydroxy-CBD.

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Year:  1976        PMID: 6714     DOI: 10.1111/j.2042-7158.1976.tb04152.x

Source DB:  PubMed          Journal:  J Pharm Pharmacol        ISSN: 0022-3573            Impact factor:   3.765


  2 in total

1.  Microbiological oxidation of the pentyl side chain of cannabinoids.

Authors:  L W Robertson; S W Koh; S R Huff; R K Malhotra; A Ghosh
Journal:  Experientia       Date:  1978-08-15

2.  Metabolism of cannabidiol by the rat.

Authors:  E Samara; M Bialer; D J Harvey
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1991 Oct-Dec       Impact factor: 2.441

  2 in total

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