(S)-2,3-Oxidosqualene ((S)-2,3-epoxysqualene) is an intermediate in the synthesis of the cell membrane sterol precursors lanosterol and cycloartenol, as well as saponins. It is formed when squalene is oxidized by the enzyme squalene monooxygenase. 2,3-Oxidosqualene is the substrate of various oxidosqualene cyclases, including lanosterol synthase, which produces lanosterol, a precursor to cholesterol.[1]
Names | |
---|---|
Preferred IUPAC name
2,2-Dimethyl-3-[(3E,7E,11E,15E)-3,7,12,16,20-pentamethylhenicosa-3,7,11,15,19-pentaen-1-yl]oxirane | |
Other names
Squalene oxide
2,3-Squalene oxide Squalene epoxide Squalene-2,3-epoxide | |
Identifiers | |
3D model (JSmol)
|
|
ChEBI | |
ChemSpider | |
MeSH | 2,3-oxidosqualene |
PubChem CID
|
|
UNII | |
CompTox Dashboard (EPA)
|
|
| |
| |
Properties | |
C30H50O | |
Molar mass | 426.717 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
The stereoisomer (R)-2,3-oxidosqualene is an inhibitor of lanosterol synthase.
References
edit- ^ Abe I. (2007). "Enzymatic synthesis of cyclic triterpenes". Natural Product Reports. 24 (6): 1311–31. doi:10.1039/b616857b. PMID 18033581.