Dinosterol
| Names | |
|---|---|
| IUPAC name
(22E)-4α,23-Dimethyl-5α-ergost-22-en-3β-ol
| |
| Systematic IUPAC name
(1R,3aS,3bS,5aS,6S,7S,9aR,9bS,11aR)-6,9a,11a-Trimethyl-1-[(2R,3E,5R)-4,5,6-trimethylhept-3-en-2-yl]hexadecahydro-1H-cyclopenta[a]phenanthren-7-ol | |
| Identifiers | |
3D model (JSmol)
|
|
| ChemSpider | |
PubChem CID
|
|
| UNII | |
CompTox Dashboard (EPA)
|
|
| |
| |
| Properties | |
| C30H52O | |
| Molar mass | 428.745 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
| |
Dinosterol (4α,23,24-trimethyl-5α-cholest-22E-en-3β-ol) is a 4α-methyl sterol that is produced by several genera of dinoflagellates and is rarely found in other classes of protists. The steroidal alkane, dinosterane, is the 'molecular fossil' of dinosterol, meaning that dinosterane has the same carbon skeleton as dinosterol, but lacks dinosterol's hydroxyl group and olefin functionality. As such, dinosterane is often used as a biomarker to identify the presence of dinoflagellates in sediments.