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Cannabis sativa synthesis

Szirmai M (1995) Total synthesis and analysis of major human urinary metabolites of dl-tetrahydrocannabinol, the principal psychoactive component of Cannabis sativa L. Dissertation, Uppsala University, Sweden... [Pg.40]

Biotransformation of (+)- and -)-cis/trans- etheno s to (-f)-verbenone has been achieved by a cell-free system of Cannabis sativa Callus.The (—)- and (+)-verbenone (via verbenol) were the starting materials for the first synthesis of the (—)- and (+)- enantiomers of A -tetrahydrocannabinol. [Pg.166]

A -3,4-cis-THC has now been found in Cannabis sativa (Phenotype III) other papers reporting the characterization of compounds from Cannabis sativa concern conclusive identification and synthesis of cannabinodiol, " which is known to result from the photochemical irradiation of cannabinol (Vol. 7, p. 51), and the identification of A -tetrahydrocannabinolic acid " and (+)-cannabitriol (263) " (263) and the corresponding C-2 ethyl ether may be epoxide-derived. " ... [Pg.61]

The opium alkaloids codeine and morphine served as models for the synthesis of naloxone, an important analog used to treat and diagnose opiate addicts, and also led to the discovery of endogenous opioids (enkephalins and endorphins) (see Chapter 47). Similarly, A9-tetrahydro-cannabinol (THC), the component of Cannabis sativa responsible for the central nervous system (CNS) effect, has also been found to reduce nausea associated with cancer chemotherapy (see Chapter 18). [Pg.49]

Delta-9-THC is the main active constituent extracted from Cannabis sativa (Tuner, 1985 in Marijuana 1984, Ed. Harvey, DY, IRL Press, Oxford). Numerous articles have described not only psychotropic effects of cannabinoids but also their influence on the immune function [Hollister L. E., J. Psychoact. Drugs 24 (1992) 159-164]. The majority of in vitro studies have shown that cannabinoids have immunosuppressant effects inhibition of the mitogen induced proliferative responses of T lymphocytes and B lymphocytes [Luo, Y. D. et ah, Int. J. Immuno-pharmacol. (1992) 14,49-56 Schwartz, H. et at., J. Neuroimmunol. (1994) 55,107-115], inhibition of the activity of cytotoxic T cells [Klein et at., J. Toxicol. Environ. Health (1991) 32, 465-477], inhibition of the microbicidal activity of macrophages and of TNF-a synthesis [Arata, S. et at.. Life Sci. (1991) 49, 473-479 Fisher-Stenger et al., J. Pharm. Exp. Then (1993) 267, 1558-1565] and inhibition of the cytolytic activity and the TNFa production of large granular lymphoc3rtes [Kusher et al.. Cell. Immun. (1994) 154, 99-108],... [Pg.35]

Natural ligands for the cannabinoid receptors CB, and CB2, so named because they bind the active ingredient delta -tetrahydrocannabinol in Cannabis sativa, include arachi-donoyl glycerol and also 2-arachidonoyl glycerol ether. The metabolic steps that form this unusual ether lipid are unknown since the synthesis of sn-2 glycerol ethers has not been studied to date. [Pg.255]

Lousberg RJC, Bercht CAL, Van Ooyen R, Spronck HJW (1977) Cannabinodiol conclusive identification and synthesis of a new cannabi-noid from Cannabis sativa. Phytochemistry 16 595... [Pg.3432]


See other pages where Cannabis sativa synthesis is mentioned: [Pg.103]    [Pg.58]    [Pg.95]    [Pg.210]    [Pg.661]    [Pg.264]    [Pg.113]    [Pg.537]    [Pg.245]    [Pg.296]   
See also in sourсe #XX -- [ Pg.16 , Pg.492 ]




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Cannabis sativa

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