Structure via PubChem · Public domain (PubChem)
9xi-episterol
Sign in to saveEpisterol is a sterol involved in the biosynthesis of steroids. Episterol is synthesized from 24-methylenelophenol. Episterol is converted to 5-dehydroepisterol by ERG3, the C-5 sterol desaturase in the yeast. Episterol is also known to be a precursor to ergosterol.
Chemical data
- Formula
- C28H46O
- Molecular weight
- 398.7 g/mol
- IUPAC name
- (3S,5S,10S,13R,14R,17R)-10,13-dimethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
- SMILES
- C[C@H](CCC(=C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CCC3C2=CC[C@@H]4[C@@]3(CC[C@@H](C4)O)C)C
- InChIKey
- BTCAEOLDEYPGGE-LPWCLQGBSA-N
- XLogP
- 8.4
- Polar surface area
- 20.2 Ų
- H-bond donors
- 1
- H-bond acceptors
- 1
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 398.355
Show 4 more facts
- chemical formula
- C₂₈H₄₆O
- canonical SMILES
- CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C
- isomeric SMILES
- C[C@H](CCC(=C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CCC3C2=CC[C@@H]4[C@@]3(CC[C@@H](C4)O)C)C
- Commons category
- Episterol
Sources (1)
via Wikidata · CC0
~1 min read
Encyclopedic overview
2 sectionsContents
- References
- External links
Episterol is a sterol involved in the biosynthesis of steroids. Episterol is synthesized from 24-methylenelophenol. Episterol is converted to 5-dehydroepisterol by ERG3, the C-5 sterol desaturase in the yeast. Episterol is also known to be a precursor to ergosterol.
==References==
Excerpted from Wikipedia’s “9xi-episterol” article, available under the CC BY-SA 4.0 licence.