Triterpene: Difference between revisions

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[[Category:Terpenes and terpenoids]]
[[Category:Terpenes and terpenoids]]
[[Category:Biochemistry]]
[[Category:Biochemistry]]
<gallery>
File:Squalene.svg|Squalene
File:Hopane.svg|Hopane
File:Cholesterol.svg|Cholesterol
</gallery>

Latest revision as of 01:36, 18 February 2025

Class of chemical compounds


Chemical Compound
Identifiers
CAS Number
PubChem CID
ChemSpider ID
UNII
ChEBI
ChEMBL
Properties
Chemical Formula
Molar Mass
Appearance
Density
Melting Point
Boiling Point
Hazards
GHS Pictograms [[File:|50px]]
GHS Signal Word
GHS Hazard Statements
NFPA 704 [[File:|50px]]
References

Triterpenes are a class of terpenes consisting of six isoprene units and having the molecular formula C30H48. They are found in a wide variety of plants and animals and are the precursors to steroids in both plants and animals.

Structure and biosynthesis[edit]

Triterpenes are synthesized via the mevalonate pathway in eukaryotes and some bacteria. The process begins with the condensation of two molecules of farnesyl pyrophosphate to form squalene, a linear triterpene. Squalene can then undergo cyclization to form various triterpene structures, such as hopane and lanosterol, the latter being a precursor to cholesterol and other steroids.

Functions and occurrence[edit]

Triterpenes serve various functions in plants and animals. In plants, they often act as defense mechanisms against herbivores and pathogens. In animals, triterpenes like cholesterol are crucial components of cell membranes and precursors to hormones.

Triterpenes are also found in fungi and bacteria, where they can play roles in cellular structure and metabolism.

Examples of triterpenes[edit]

Applications[edit]

Triterpenes have various applications in medicine and cosmetics. They are studied for their potential anti-inflammatory, antiviral, and anticancer properties. Some triterpenes are used in traditional medicine and as dietary supplements.

Related pages[edit]

References[edit]