Taxane
Taxanes are diterpenes produced by the plants of the genus Taxus (yews) featuring a taxadiene core. They are widely used as chemotherapy agents.[1][2] Taxane agents include paclitaxel (Taxol) and docetaxel (Taxotere). In 2010 another Taxane, cabazitaxel was FDA approved to treat hormone-refractory prostate cancer.
Taxanes present difficulties in formulation as medicines because they are poorly soluble in water.
Production
As their name suggests, taxanes were first derived from natural sources, but some have been synthesized artificially. Paclitaxel was originally derived from the Pacific yew tree. Taxanes are difficult to synthesize because of their numerous chiral centres — Taxol has 11 of these.
Mechanism of action
The principal mechanism of action of the taxane class of drugs is the disruption of microtubule function. Microtubules are essential to cell division, and taxanes stabilize GDP-bound tubulin in the microtubule, thereby inhibiting the process of cell division as depolymerization is prevented. Thus, in essence, taxanes are mitotic inhibitors. In contrast to the taxanes, the vinca alkaloids prevent mitotic spindle formation through inhibition of tubulin polymerisation. Both taxanes and vinca alkaloids are, therefore, named spindle poisons or mitosis poisons, but they act in different ways. Taxanes are also thought to be radiosensitizing.
Substances
Hongdoushans A-C are oxygenated taxane diterpenes, isolated from the wood of Taxus wallichiana. Hongdoushan A (C29H44O7), hongdoushan B (C27H40O7), and hongdoushan C (C27H42O6) are reported to have anticancer activity in vitro.[3]
See also
References
External links
Media related to Lua error in package.lua at line 80: module 'strict' not found. at Wikimedia Commons
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