Paclitaxel

3Citations
Citations of this article
553Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Paclitaxel belongs to diterpenoid compound and the main natural source of it is yew bark. Docetaxel is the main derivative of paclitaxel and artificially synthesized on the base of the structure of paclitaxel. Paclitaxel and docetaxel showed potent suppression to most solid tumors and gained the highest sales among all the antitumor drugs in the world due to its specific mechanism. The main target of paclitaxel is microtubule in cells. Compared with paclitaxel, docetaxel shows stronger affinity to tubulin and longer retention time in cells. Paclitaxel is mainly metabolized through the liver and eliminated from the body by feces. Paclitaxel showed no obvious toxic effects on main organs, and its clinical side effects include allergic reactions, nervous system damage, hematopoietic suppression, catarrh, and cardiac toxicity.

Author supplied keywords

Cite

CITATION STYLE

APA

Wang, L., & Du, G. H. (2018). Paclitaxel. In Natural Small Molecule Drugs from Plants (pp. 537–544). Springer Singapore. https://doi.org/10.1007/978-981-10-8022-7_89

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free