2013;133(10):1093-101.
[Medicinal chemistry and pharmacology focused on cannabidiol, a major component of the fiber-type cannabis].
[Article in Japanese]
Abstract
Considerable attention has focused on cannabidiol (CBD), a major non-psychotropic constituent of fiber-type cannabis plant, and it has been reported to possess diverse biological activities. Although CBD is obtained from non-enzymatic decarboxylation of its parent molecule, cannabidiolic acid(CBDA), several studies have investigated whether CBDA itself is biologically active. In the present report, the author summarizes findings indicating that; 1) CBDA is a selective cyclooxygenase-2 (COX-2) inhibitor, and ii) CBDA possesses an anti-migrative potential for highly invasive cancer cells, apparently through a mechanism involving inhibition of cAMP-dependent protein kinase A, coupled with an activation of the small GTPase, RhoA. Further, the author introduces recent findings on the medicinal chemistry and pharmacology of the CBD derivative, CBD-2′,6′-dimethyl ether (CBDD), that exhibits inhibitory activity toward 15-lipoxygenase (15-LOX), an enzyme responsible for the production of oxidized low-density lipoprotein (LDL). These studies establish CBD as both an important experimental tool and as a lead compound for pharmaceutical development. In this review, the author further discusses the potential uses of CBD and its derivatives in future medicines.
- PMID:
24088353
[PubMed – indexed for MEDLINE]
Publication Types, MeSH Terms, Substances
Publication Types
MeSH Terms
- Animals
- Breast Neoplasms/pathology
- Cannabidiol/analogs & derivatives
- Cannabidiol/chemistry*
- Cannabidiol/pharmacology*
- Cannabinoids/chemistry
- Cannabis/chemistry*
- Cell Movement/drug effects
- Cells, Cultured
- Chemistry, Pharmaceutical*
- Cyclic AMP-Dependent Protein Kinases/antagonists & inhibitors
- Cyclooxygenase 2 Inhibitors
- Decarboxylation
- Drug Discovery
- Female
- Humans
- Lipoproteins, LDL/biosynthesis
- Lipoxygenase Inhibitors
- Phytotherapy*
- rhoA GTP-Binding Protein/metabolism
Substances
LinkOut – more resources
Full Text Sources
Medical