Triterpenes are a class of terpenes composed of six isoprene units with the molecular formula C30H48; they may also be thought of as consisting of three terpene units. Animals, plants and fungi all produce triterpenes, including squalene, the precursor to all .
Structures
Triterpenes exist in a great variety of structures. Nearly 200 different skeletons have been identified.
These skeletons may be broadly divided according to the number of rings present. In general pentacyclic structures (5 rings) tend to dominate.
Squalene is biosynthesized through the head-to-head condensation of two farnesyl pyrophosphate units. This coupling converts a pair of C15 components into a C30 product. Squalene serves as precursor for the formation of many triterpenoids, including bacterial hopanoids and eukaryotic .
Triterpenoids
By definition triterpenoids are triterpenes that possess
, usually oxygen. The terms
triterpene and
triterpenoid often are used interchangeably.
Triterpenoids possess a rich chemistry and pharmacology with several pentacyclic motifs. Lupane, oleanane and ursane show particular promise as anti-cancer agents.
Steroids
Steroids feature a
cucurbitane core, although in practice they are biosynthesised from either
lanosterol (animals and fungi) or
cycloartenol (plants) via the cyclization of
squalene. Steroids have two principal biological functions, being either key components of cell membranes or signaling molecules that activate steroid hormone receptors. Important sub-classes include
and
.
Triterpenoid saponins
Triterpenoid saponins are triterpenes which belong to the
saponin group of compounds, making them triterpenoid
. They are produced by plants as part of their self-defense mechanism
with important sub-classes including
and
.
