10-Deacetylbaccatin
Chemical compound used in the synthesis of paclitaxel
10-Deacetylbaccatin III is a naturally occurring diterpene found in the yew tree, specifically in the Taxus species. It is a crucial intermediate in the semisynthesis of the anticancer drug paclitaxel, commonly known as Taxol.
Structure and Properties[edit | edit source]
10-Deacetylbaccatin III is a complex diterpene with a molecular formula of C31H38O10. It is characterized by its tetracyclic ring structure, which is a hallmark of the taxane family of compounds. The compound is named for the absence of an acetyl group at the C-10 position, distinguishing it from other related taxanes.
Biosynthesis[edit | edit source]
10-Deacetylbaccatin III is biosynthesized in the Taxus species through a series of enzymatic reactions starting from the precursor geranylgeranyl pyrophosphate. The biosynthetic pathway involves multiple steps, including cyclization, oxidation, and acylation, leading to the formation of the taxane core structure.
Role in Paclitaxel Synthesis[edit | edit source]
10-Deacetylbaccatin III serves as a key starting material in the semisynthetic production of paclitaxel. The semisynthesis involves the attachment of a side chain to the C-13 position of the taxane core, which is essential for the biological activity of paclitaxel. This process allows for the large-scale production of paclitaxel, which is used in the treatment of various cancers, including ovarian cancer, breast cancer, and non-small cell lung cancer.
Extraction and Isolation[edit | edit source]
The compound is typically extracted from the needles and bark of the Taxus baccata and Taxus brevifolia species. The extraction process involves organic solvents and chromatographic techniques to isolate 10-Deacetylbaccatin III in its pure form. Due to the limited availability of natural sources, research into alternative methods of production, such as plant cell culture and biotechnological synthesis, is ongoing.
Applications in Research[edit | edit source]
Beyond its role in paclitaxel synthesis, 10-Deacetylbaccatin III is studied for its potential biological activities and as a scaffold for the development of novel taxane derivatives. Researchers are exploring modifications to the taxane core to enhance its pharmacological properties and reduce side effects associated with paclitaxel treatment.
Related pages[edit | edit source]
Search WikiMD
Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD
WikiMD's Wellness Encyclopedia |
Let Food Be Thy Medicine Medicine Thy Food - Hippocrates |
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian
Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.
Contributors: Prab R. Tumpati, MD