Related Experiment Video
Updated: Dec 21, 2025

Carotid Artery Infusions for Pharmacokinetic and Pharmacodynamic Analysis of Taxanes in Mice
Published on: October 27, 2014
Two-Phase Synthesis of Taxol
Yuzuru Kanda1, Hugh Nakamura1, Shigenobu Umemiya1
1Department of Chemistry, Scripps Research, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
Researchers developed a novel divergent synthetic approach to produce paclitaxel (Taxol). This method, inspired by natural terpene biosynthesis, offers a new pathway for Taxol synthesis, complementing existing supply methods.
Area of Science:
- Natural Product Chemistry
- Organic Synthesis
- Medicinal Chemistry
Background:
- Paclitaxel (Taxol) is a highly successful anticancer drug derived from natural sources.
- Initial supply concerns for paclitaxel spurred extensive research into its total synthesis.
- Current paclitaxel production relies on plant-derived or biosynthetically produced material.
Purpose of the Study:
- To explore a novel synthetic strategy for paclitaxel (Taxol) production.
- To develop a divergent synthetic approach inspired by natural biosynthetic pathways.
- To offer an alternative method for accessing synthetic paclitaxel.
Main Methods:
- A complementary divergent synthetic strategy was designed.
- The approach was holistically patterned off of terpene biosynthetic machinery.
- Synthetic routes were developed to access paclitaxel.
Main Results:
- Demonstrated the feasibility of a novel divergent synthetic approach for paclitaxel.
- The synthetic strategy mimics natural biosynthetic processes for terpene synthesis.
- This method provides a new route to synthetic paclitaxel.
Conclusions:
- A novel divergent synthetic approach can be used to synthesize paclitaxel (Taxol).
- This method complements existing natural and biosynthetic supply strategies.
- The findings open new avenues for the synthesis of complex natural products.
Related Concept Videos
Drugs that Stabilize Microtubules
Preparation of Diols and Pinacol Rearrangement
The reaction begins with transferring a proton from the acid catalyst to one of the hydroxyl groups, producing an oxonium ion.
Phase II Conjugation Reactions: Overview
Phase II Reactions: Miscellaneous Conjugation Reactions
A key example involves the conjugation of cyanide ions, which impair cellular respiration and alter hemoglobin into non-oxygen-carrying cyanmethemoglobin. To neutralize this threat, a sulfur atom from thiosulphate is transferred to the cyanide ion, catalyzed by the enzyme rhodanese, resulting in an inactive compound called thiocyanate. The production of...

