Structure via PubChem · Public domain (PubChem)
ارگوسترول
Sign in to saveAlso known as (22E,24S)-24-methylcholesta-5,7,22-trien-3beta-ol, Ergosta-5,7,22-trien-3beta-ol, 24alpha-Methyl-22E-dehydrocholesterol, Ergosterin, Ergosta-5,7,22-trien-3-ol, (3beta,22E)-, 24R-Methylcholesta-5,7,2E-trien-3beta-ol, (3S,9S,10R,13R,14R,17R)-10,13-dimethyl-17-[(E,1R,4R)-1,4,5-trimethylhex-2-enyl]-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol, (3S,9S,10R,13R,14R,17R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol
ترکیب شیمیایی
OverviewAI-generated
Ergosterol is a chemical compound with the formula C₂₈H₄₄O. Its mass is listed as 396.339, while its weight is recorded as 396.6. The substance has a charge of 0 and an xlogp value of 7.4. It features one hydrogen bond donor and one hydrogen bond acceptor, with a topological polar surface area of 20.2.
The compound is associated with a PubMed query count of 8088. It is referenced by 468 other encyclopedia articles.
Synthesized by Vinony from 18 facts across 4 sources: Wikidata, PubMed, PubChem, Vinony graph. Generated from structured data (not the Wikipedia text) and checked against those facts — may still contain errors.
Chemical data
- Formula
- C28H44O
- Molecular weight
- 396.6 g/mol
- IUPAC name
- (3S,9S,10R,13R,14R,17R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol
- SMILES
- C[C@H](/C=C/[C@H](C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3C2=CC=C4[C@@]3(CC[C@@H](C4)O)C)C
- InChIKey
- DNVPQKQSNYMLRS-APGDWVJJSA-N
- XLogP
- 7.4
- Polar surface area
- 20.2 Ų
- H-bond donors
- 1
- H-bond acceptors
- 1
- Formal charge
- 0
via PubChem
Research
8,088 papers- Regulation of Ergosterol Biosynthesis in Saccharomyces cerevisiae.Genes · 2020
- Ergosterol and Lanosterol Derivatives: Synthesis and Possible Biomedical Applications.ChemMedChem · 2025
- Outline of the biosynthesis and regulation of ergosterol in yeast.World journal of microbiology & biotechnology · 2019
- Ergosterol Peroxide: A Mushroom-Derived Compound with Promising Biological Activities-A Review.International journal of medicinal mushrooms · 2017
- Ergosterol-loaded brain-targeted liposomes attenuate stroke via gut microbiota-metabolite-brain axis modulation.Journal of nanobiotechnology · 2025
via PubMed
Wikidata facts
- Mass
- 396.339
Show 6 more facts
- found in taxon
- Saccharomyces cerevisiae
- chemical formula
- C₂₈H₄₄O
- isomeric SMILES
- C[C@H](/C=C/[C@H](C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3C2=CC=C4[C@@]3(CC[C@@H](C4)O)C)C
- canonical SMILES
- CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C
- subject has role
- provitamin
- Commons category
- Ergosterol
Sources (7)
via Wikidata · CC0