SESTERPENES

They are derived from geranylfarnesol pyrophosphate and have 25 carbon atoms. They were isolated from insect protective waxes and from fungal sources.

Three examples of sesterpenes are shown below.

Variously unsaturated and branched sesterpenes, known as Haslenes, were found in species of diatomaceous algae (Volkman JK at el., Organic Geochem 1994, 21, 407).They are widely distributed and abundant in marine sediments. Several haslenes were found to be produced by a pennate diaton Haslea ostrearia according to the culture temperature and were shown to have cytostatic properties (Rowland SJ et al., Phytochemistry 2001, 56, 597). One of them is shown below.

TRITERPENOIDS

They form a large group of natural substances which includes steroids and consequently sterols. Squalene is the immediate biological precursor of all triterpenoids. 

The large group of steroids, including sterols, are present in very small amounts in bacteria but at larger amounts in plants and animals while the hopanoids are very abundant in prokaryotes where they replace cholesterol. 

Among the large number of triterpenoid structures,  some of them are shown below.

Steroids are modified triterpenes which derived also from squalene by cyclization, unsaturation and substitution. The nucleus of all steroids is the tetracyclic C17 hydrocarbon 1,2-cyclopentanoperhydrophenanthrene (gonane or sterane) substituted by methyl groups at C10 and C13, as well as an alkyl side-chain at C17. Steroids may possess a nucleus derived from the former one by one or more C-C bond scissions or ring expansions or contractions.
Gonane and three examples of basic unsubstituted steroids are shown below.

Unsaturated steroids with most of the skeleton of cholestane containing a 3b-hydroxyl group and an aliphatic side chain of 8 or more carbon atoms attached to position 17 form the group of sterols.

The hopanoïds are pentacyclic triterpenoids based on the hopane skeleton (with a five-membered ring E)  are widely distributed in prokaryotes but were not detected in Archaea (Rohmer M et al., J Gen Microbiol 1984, 130, 1137). In most cases, the hopanoid content of the cell is comparable with the cholesterol content of eukaryotic cells. They are considered as membrane rigidifiers. Furthermore, they are the precursors of several derived compounds (homohopanoids) in sediments and oils (Ourisson G et al., Pure Appl Chem 1979, 51, 709) and thus could be considered as the most abundant natural products on earth (Ourisson G et al., Accounts Chem Res 1992, 25, 398). Hopanoids occur predominantly in aerobic bacteria (methanotrophs, heterotrophs and cyanobacteria) but have also been found in some anaerobic bacteria (Sinninghe Damsté JS et al., Org Chem 2004, 35, 561).

The simplest C30 hopanoid is diploptene.

The most abundant hopanoids in prokaryotes are C35 bacteriohopanepolyols in which the side-chain of the parent structure contains a variable number of vicinal hydroxyl groups

The hopanoids are widely distributed in bacteria and blue-green algae where they are important cell membrane constituents. It is often said that hopanoids are the "most abundant natural products on Earth".
As hopanoids are very stable and are not easily degraded, they are receiving an intense attention as biological markers with applications for geochemical studies of petroleum source rocks and oils. These biomarkers are mainly derived from bacterial bacteriohopanepolyols (biohopanoids). Different bacterial groups possess recognizable biohopanoid distributions, giving hopanoids marker potential for specific bacterial populations and environmental conditions. More than 150 individual hopane derivatives have been isolated from various types of sedimentary organic matter.

Other pentacyclic triterpenoids based on the lupane skeleton include a very large number of naturally occurring members with different functional groups which are found in vegetables and fruit. Among them, lupeol is one of the most ubiquitous compounds. 

Lupeol was shown to have various pharmacological properties, inducing anti-inflammatory and anti-arthritic responses and inhibition of tumor growth (Saleem M et al., Cancer Res 2005, 65, 11203) in animal cells.
Long-chain fatty acid esters (C20, C22 and C26) of lupeol extracted from an African plant, Holarrhena floribunda (Apocynaceae), were shown to have strong antimalarial activity, especially against drug-resistant strains of Plasmodium falciparum (Fotie J et al., J Nat Prod 2006, 69, 62). 
Fatty acid esters (palmitic or stearic acid) of lupeol have been isolated from green propolis produced by honeybees from vegetative apices of the Asteraceae Baccharis dracunculifolia from Brazil (Furukawa S et al., Chem Pharm Bull 2002, 50, 439). These compounds were named procrim a and b.

Palmitic acid ester of lupeol (Procrim a)

In contrast with the hopane series, which possesses a five-membered ring E, the gammacerane skeleton is characterized by a six-membered ring (see below).

Tetrahymanol (gammaceran-21a-ol), a typical representative of the series, was first isolated from the ciliate protozoan Tetrahymena pyriformis (Mallory FB et al., J Am Chem Soc 1963, 85, 1362). Later, it was detected in a number of other eukaryotes, e.g. in ferns, fungi and some other ciliates. Its occurrence was long thought to be restricted to eukaryotes but its presence in sediments pointed out a much more widespread distribution in living organisms. The finding of tetrahymanol in the purple nonsulfur bacterium Rhodopseudomonas palustris opened new insights into the biochemistry of these molecules in bacteria (Kleemann G et al., J Gen Microbiol 1990, 136, 2551). Tetrahymanol and novel methylated homologues were discovered in nitrogen-fixing bacterium Bradyrhizobium japonicum (Bravo JM et al., Eur J Biochem 2001, 268, 1323).
Gammacerane structures were shown to be reliable geochemical indicators for water column stratification in marine or in lacustrine deposits (Sinninghe Damste JS et al., Geochim Cosmochim Acta 1995, 59, 1895).