Sesquiterpene

Short description: Class of terpenes

Big Sagebrush (Artemisia tridentata) contains sesquiterpene lactones which are sesquiterpenoids (built from three isoprene units) and contain a lactone ring, hence the name. These compounds are found in many other plants and can cause allergic reactions and toxicity if consumed in excess, particularly in grazing livestock. Phallus indusiatus, in Cooktown, Queensland, Australia, which produces two unique sesquiterpenes

Sesquiterpenes are a class of terpenes that consist of three isoprene units and often have the molecular formula C15H24. Like monoterpenes, sesquiterpenes may be cyclic or contain rings, including many unique combinations. Biochemical modifications such as oxidation or rearrangement produce the related sesquiterpenoids.[1] A recent study conducted in the Cosmics Leaving Outdoor Droplets large cloud chamber at CERN, has identified sesquiterpenes—gaseous hydrocarbons that are released by plants—as potentially playing a major role in cloud formation in relatively pristine regions of the atmosphere.[2]

## Contents

* 1 Biosynthesis and examples
* 1.1 Sesquiterpenoids
* 2 References
* 3 External links

## Biosynthesis and examples

The reaction of geranyl pyrophosphate with isopentenyl pyrophosphate results in the 15-carbon farnesyl pyrophosphate (FPP), which is an intermediate in the biosynthesis of sesquiterpenes such as farnesene.[3][4]

Farnesyl pyrophosphate

Cyclic sesquiterpenes are more common than cyclic monoterpenes because of the increased chain length and additional double bond in the sesquiterpene precursors. In addition to common six-membered ring systems such as the ones found in zingiberene and bisacurone, cyclization of one end of the chain to the other end can lead to macrocyclic rings such as humulene.

Zingiberene, a sesquiterpene abundant in ginger. δ-Cadinene, one of a family of sesquiterpene. Humulones are sesquiterpenoids that give "hoppy" flavor to beer.

The cadinenes contain two fused six-membered rings. Caryophyllene, a component of many essential oils such as clove oil, contains a nine-membered ring fused to a cyclobutane ring. Rishitin is another example of a cadinene, which is found in potatoes and tomatoes.[5][6]

Vetivazulene and guaiazulene are aromatic bicyclic sesquiterpenoids.

With the addition of a third ring, the possible structures become increasingly varied. Examples include longifolene, copaene and the alcohol patchoulol.

### Sesquiterpenoids

The FPP backbone can be rearranged in several different ways and further decorated with different functional groups, hence the large variety of sesquiterpenoids. Geosmin, the volatile compound that gives an earthy taste and musty odor in drinking water and the characteristic odor on a rainy day, is a sesquiterpenoid, produced by bacteria, especially cyanobacteria, that are present in the soils and water supplies.[7] Oxidation of farnesene then provides the sesquiterpenoid farnesol.

Sesquiterpene lactones are a common class of sesquiterpenoids that contain a lactone ring, hence the name. They are found in many plants and can cause allergic reactions and toxicity if consumed excessively, particularly in grazing livestock.[8]

The term merosesquiterpenoids was coined in 1968 to describe molecules of this class that have a mixed biosynthetic origin, meaning isoprenoid precursors like isopentenyl pyrophosphate are derived from both the mevalonate and non-mevalonate pathways.[9]

## References

1. ↑ Eberhard Breitmaier (2006). "Sesquiterpenes". Terpenes: Flavors, Fragrances, Pharmaca, Pheromones. pp. 24–51. doi:10.1002/9783527609949.ch3. ISBN 9783527609949.
2. ↑ Dada, Lubna; Stolzenburg, Dominik; Simon, Mario; Fischer, Lukas; Heinritzi, Martin; Wang, Mingyi; Xiao, Mao; Vogel, Alexander L. et al. (2023). "Role of sesquiterpenes in biogenic new particle formation" (in en). Science Advances 9 (36). doi:10.1126/sciadv.adi5297. PMID 37682996.
3. ↑ Davis, Edward M.; Croteau, Rodney (2000). "Cyclization Enzymes in the Biosynthesis of Monoterpenes, Sesquiterpenes, and Diterpenes". Topics in Current Chemistry 209: 53–95. doi:10.1007/3-540-48146-X_2. ISBN 978-3-540-66573-1.
4. ↑ Chizzola, Remigius (2013), "Regular Monoterpenes and Sesquiterpenes (Essential Oils)", Natural Products (Springer Berlin Heidelberg): pp. 2973–3008, doi:10.1007/978-3-642-22144-6_130, ISBN 9783642221439
5. ↑ Katsui, N.; Murai, A.; Takasugi, M.; Imaizumi, K.; Masamune, T.; Tomiyama, K. (1968). "The structure of rishitin, a new antifungal compound from diseased potato tubers" (in en). Chemical Communications (1): 43–44. doi:10.1039/C19680000043.
6. ↑ D’Harlingue, A., Mamdouh, A. M., Malfatti, P., Soulie, M.-C., & Bompeix, G. (1995). Evidence for rishitin biosynthesis in tomato cultures. Phytochemistry, 39(1), 69–70. https://doi.org/10.1016/0031-9422(94)00844-J
7. ↑ "Geosmin and 2-methylisoborneol production in a major aqueduct system". Water Science and Technology 31 (11): 41–48. June 1995. doi:10.1016/0273-1223(95)00454-u.
8. ↑ "Sesquiterpene Lactones and their toxicity to livestock". Cornell University. http://poisonousplants.ansci.cornell.edu/toxicagents/sesqlactone/sesqlactone.html.
9. ↑ Simpson, Thomas J.; Ahmed, Salman A.; Rupert McIntyre, C.; Scott, Fiona E.; Sadler, Ian H. (1997-03-17). "Biosynthesis of polyketide-terpenoid (meroterpenoid) metabolites andibenin B and andilesin A in Aspergillus variecolor" (in en). Tetrahedron 53 (11): 4013–4034. doi:10.1016/S0040-4020(97)00015-X. ISSN 0040-4020. http://www.sciencedirect.com/science/article/pii/S004040209700015X.

## External links

| Look up sesquiterpene in Wiktionary, the free dictionary.

|

* Sesquiterpenes at the US National Library of Medicine Medical Subject Headings (MeSH)

* v
* t
* e

Types of terpenes and terpenoids (# of isoprene units)

Basic forms:|

* Acyclic (linear, cis and trans forms)
* Monocyclic (single ring)
* Bicyclic (2 rings)
* Iridoids (cyclopentane ring)
* Iridoid glycosides (iridoids bound to a sugar)
* Steroids (4 rings)

Hemiterpenoids (1)|

* Isoprene (C5H8)
* Prenol
* Isovaleric acid

Monoterpene (C10H16)(2)|

| Acyclic|

* Ocimene
* Myrcenes

|

Monocyclic|

* Limonene
* Terpinene
* Phellandrene
* Umbellulone

Bicyclic|

* Pinene (β and α)
* Camphene
* Thujene
* Sabinene
* Carene

Monoterpenoids (2,modified)|

| Acyclic|

* Linalool
* Citronellal
* Citral
* Citronellol
* Geraniol
* Geranyl pyrophosphate

|

Monocyclic|

* Grapefruit mercaptan
* menthol
* p-Cymene
* thymol
* Perillyl alcohol
* Carvacrol

Bicyclic|

* Camphor
* Borneol
* Eucalyptol
* Halomon
* Pinene
* Ascaridole

Sesquiterpenoids (3)|

* Farnesyl pyrophosphate
* Artemisinin
* Bisabolol

Diterpenoids (4)|

* Geranylgeranyl pyrophosphate
* Gibberellin
* Retinol
* Retinal
* Phytol
* Taxol
* Forskolin
* Aphidicolin
* Salvinorin A

Sesterterpenoids (5)|

* geranylfarnesol

Triterpenoids (6)|

| Steroids|

* Phytosterols
* Campesterol
* beta Sitosterol
* gamma sitosterol
* Stigmasterol
* Tocopherols
* Cholesterol
* Testosterone
* Cholecalciferol (Vit D)
* Ecdysones

|

Other|

* Saponins
* Squalane
* Lanosterol
* Acids
* Oleanolic acid
* Ursolic acid
* Betulinic acid
* Moronic acid

Sesquarterpenes/oids (7)|

* ferrugicadiol
* tetraprenylcurcumene

Tetraterpenoids
(Carotenoids) (8)|

| Carotenes|

* Alpha-Carotene
* Beta-Carotene
* Gamma-Carotene
* Delta-Carotene
* Lycopene
* Neurosporene
* Phytofluene
* Phytoene

|

Xanthophylls:|

* Canthaxanthin
* Cryptoxanthin
* Zeaxanthin
* Astaxanthin
* Lutein
* Rubixanthin

Polyterpenoids (many)|

* sap, resins, latex of many plants, e.g. rubber

Norisoprenoids (modified)|

* 3-oxo-α-ionol
* 7,8-dihydroionone

Synthesis|

* Terpene synthase enzymes (many), having in common a Terpene synthase N terminal domain (protein domain)

Activated isoprene forms|

* Isopentenyl pyrophosphate (IPP)
* Dimethylallyl pyrophosphate (DMAPP)

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