7-Dehydrodesmosterol
Names | |
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IUPAC name Cholesta-5,7,24-trien-3β-ol | |
Systematic IUPAC name (1R,3aR,7S,9aR,9bS,11aR)-9a,11a-Dimethyl-1-[(2R)-6-methylhept-5-en-2-yl]-2,3,3a,6,7,8,9,9a,9b,10,11,11a-dodecahydro-1H-cyclopenta[a]phenanthren-7-ol | |
Other names 24-Dehydroprovitamin D3 | |
Identifiers | |
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InChI
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Properties | |
Chemical formula | C27H42O |
Molar mass | 382.62 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references |
Chemical compound
7-Dehydrodesmosterol (or cholesta-5,7,24-trien-3-beta-ol) is a cholesterol intermediate.[1]
References
- ^ Nowaczyk, MJM; Waye, JS (2001). "The Smith-Lemli-Opitz syndrome: A novel metabolic way of understanding developmental biology, embryogenesis, and dysmorphology". Clinical Genetics. 59 (6): 375–86. doi:10.1034/j.1399-0004.2001.590601.x. PMID 11453964. S2CID 9146017.
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Cholesterol and steroid metabolic intermediates
to HMG-CoA |
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Ketone bodies | |
to DMAPP | |
Geranyl- | |
Carotenoid |
- 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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