| Literature DB >> 24178215 |
H Tanaka1, R Takahashi, S Morimoto, Y Shoyama.
Abstract
Two marihuana constituents, cannabidiol (1) and cannabidiolic acid (4) were each converted mainly to two metabolites using tissue segments of Pinellia ternata tuber. The structures of the metabolites formed from 1 were determined to be 1-Oβ-D-glucopyranoside and 1-Oβ-D-diglucopyranoside by (1)H nmr, (13)C nmr and fabms. Those from 4 were determined as 4-Oβ-D-glucopyranoside and 10'-hydroxyl 4-Oβ-D-glucopyranoside. In time course experiments, 1 was absorbed rapidly by the tissues and glucosylated. Hydroxylation subsequent to the glucosylation occurred at the pentyl group in 4.Entities:
Year: 1996 PMID: 24178215 DOI: 10.1007/BF00233147
Source DB: PubMed Journal: Plant Cell Rep ISSN: 0721-7714 Impact factor: 4.570