Pregnenolone 16α-carbonitrile
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| Names | |
|---|---|
| IUPAC name
(3S,8S,9S,10R,13S,14S,16R,17S)-17-acetyl-3-hydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-16-carbonitrile | |
| Identifiers | |
| 1434-54-4 | |
| 3D model (Jmol) | Interactive image |
| ChEMBL | ChEMBL1400945 |
| ChemSpider | 14308 |
| 2762 | |
| PubChem | 15032 |
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| Properties | |
| C22H31NO2 | |
| Molar mass | 341.49 g/mol |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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| Infobox references | |
Pregnenolone 16α-carbonitrile (PCN) is a synthetic, steroidal antiglucocorticoid and pregnane X receptor agonist.[1][2][3]
See also
References
- ↑ J.I. Mason (2 September 2003). Genetics of Steroid Biosynthesis and Function. CRC Press. pp. 449–. ISBN 978-0-203-30149-4.
- ↑ Giacinto Bagetta; Marco Cosentino; Marie Tiziana Corasaniti; Shinobu Sakurada (19 April 2016). Herbal Medicines: Development and Validation of Plant-derived Medicines for Human Health. CRC Press. pp. 250–. ISBN 978-1-4398-3769-6. Cite uses deprecated parameter
|coauthors=(help) - ↑ Larisa Y. Poluektova; J. Victor Garcia-Martinez; Yoshio Koyanagi; Markus G. Manz, Andrew M. Tager (18 February 2015). Humanized Mice for HIV Research. Springer. pp. 350–. ISBN 978-1-4939-1655-9. Cite uses deprecated parameter
|coauthors=(help)
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