Estrane
Names | |
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IUPAC name 5ξ-Estrane[1] | |
Systematic IUPAC name (3aS,3bR,5aΞ,9aS,9bR,11aS)-11a-Methylhexadecahydro-1H-cyclopenta[a]phenanthrene | |
Identifiers | |
CAS Number |
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3D model (JSmol) |
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Beilstein Reference | 3125721 |
ChEBI |
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ChemSpider |
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PubChem CID |
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CompTox Dashboard (EPA) |
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InChI
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Properties | |
Chemical formula | C18H30 |
Molar mass | 246.438 g·mol−1 |
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
Estrane is a C18 steroid derivative, with a gonane core.
Estrenes are estrane derivatives that contain a double bond, with an example being nandrolone.[2] Estratrienes (estrins) are estrane derivatives that contain three double bonds, for instance estrin (estra-1,3,5(10)-triene). A class of female sex hormones, estrogens, such as estradiol, estrone, and estriol are estratrienes.
See also
References
- ^ International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 1529. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
- ^ Estrenes at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
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Steroid classification
- Estrane: Dehydrogenated: Estrene
- Estradiene
- Estratriene; Substituted: Estratrienolone
- Estratrienediol
- Estratrienetriol
- Androstane: Dehydrogenated: Androstene
- Androstadiene
- Androstatriene; Substituted: Androstanol
- Androstenol
- Androstanone
- Androstenone
- Androstanediol
- Androstenediol
- Androstanedione
- Androstenedione
- Androstenetrione
- Androstanolone
- Androstenolone
- Androstadienol
- Androstadienone; Etiocholane
- Pregnane: Dehydrogenated: Pregnene
- Pregnadiene
- Pregnatriene; Substituted: Pregnanediol
- Pregnanetriol
- Pregnenediol
- Pregnanedione
- Pregnenedione
- 5α-Pregnane
- 5β-Pregnane
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