Fecosterol
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IUPAC name 5α-Campesta-8,24(241)-dien-3β-ol | |
Systematic IUPAC name (1R,3aR,5aS,7S,9aS,11aR)-9a,11a-Dimethyl-1-[(2R)-6-methyl-5-methylideneheptan-2-yl]-2,3,3a,4,5,5a,6,7,8,9,9a,10,11,11a-tetradecahydro-1H-cyclopenta[a]phenanthren-7-ol | |
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Properties | |
Chemical formula | C28H46O |
Molar mass | 398.675 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 |
Chemical compound
Fecosterol is a sterol made by certain fungi and lichens.[1]
References
- ^ Morris, DC; Safe, S; Subden, RE (1974). "Detection of the ergosterol and episterol isomers lichesterol and fecosterol in nystatin-resistant mutants of Neurospora crassa". Biochemical Genetics. 12 (6): 459–66. doi:10.1007/BF00486063. PMID 4282021. S2CID 36287225.
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Cholesterol and steroid metabolic intermediates
to HMG-CoA |
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Ketone bodies |
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to DMAPP |
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Geranyl- |
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Carotenoid |
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- Lanosterol
- 14-demethyllanosterol
- 4alpha-Methylzymosterol
- Zymosterone
- Zymosterol
- Zymosterol
- Zymostenol
- Lathosterol
- 7-Dehydrocholesterol
- Cholesterol
- Zymosterol
- Cholesta-7,24-dien-3-ol
- 7-Dehydrodesmosterol
- Desmosterol
- Cholesterol
to Steroid hormones
- 22R-Hydroxycholesterol
- 20α,22R-Dihydroxycholesterol
- See here instead.
To Sitosterol |
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To Ergocalciferol |
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This article about a steroid is a stub. You can help Wikipedia by expanding it. |
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