Estrane
 | |
| Names | |
|---|---|
| IUPAC name
Estrane | |
| Systematic IUPAC name
15-Methyltetracyclo[8.7.0.02,7. 011,15] heptadecane | |
| Identifiers | |
| 3125721 | |
| ChEBI | CHEBI:23966  |
| ChemSpider | 11179505  4574149 (1R,2S,10R,11S,15S)-15-methyl,heptadec 5256802 (1R,2S,7R,10R,11S,15S)-15-methyl,heptadec 5256794 (1R,2S,7S,10R,11S,15S)-15-methyl,heptadec |
| Jmol 3D model | Interactive image |
| PubChem | 12313694 5460658 (1R,2S,10R,11S,15S)-15-methyl,heptadec 6857465 (1R,2S,7R,10R,11S,15S)-15-methyl,heptadec 6857457 (1R,2S,7S,10R,11S,15S)-15-methyl,heptadec |
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| Properties | |
| C18H30 | |
| Molar mass | 246.44 g·mol−1 |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| verify (what is ?) | |
| Infobox references | |
Not to be confused with estrone.
Estrane is a steroid derivative.
Estrenes are estrane derivatives that contain a double bond like nandrolone.[1]
According to some sources, an 19-nor steroid (estrane) has the advantageous property that it is more orally active than the corresponding androstane, particularly in the case of the progestin drugs since progesterone is not orally active (vs 19-Norprogesterone).[2]
See also
References
- ↑ Estrenes at the US National Library of Medicine Medical Subject Headings (MeSH)
- ↑ https://books.google.co.uk/books?id=2dBFEIiqe1cC&pg=PA149&lpg=PA149&dq=19-nor+steroids+oral+activity&source=bl&ots=1frXTAoq06&sig=aLrSBoWLmPRDdQtIFCigPnl5S5Y&hl=en&sa=X&ved=0ahUKEwjlleqZsNzKAhWEdj4KHfAZDCMQ6AEIMjAF#v=onepage&q=19-nor%20steroids%20oral%20activity&f=false
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