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| Names | |
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| IUPAC name
(25R)-Spirost-5-en-3β-ol
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| Systematic IUPAC name
(2S,2′R,4aR,4bS,5′R,6aS,6bR,7S,9aS,10aS,10bS)-4′,4a,6a,7-Tetramethyl-1,2,3,4,4a,4b,5,6,6a,6b,7,9a,10,10a,10b,11-hexadecahydrospiro[naphtho[2′,1′:4,5]indeno[2,1-b]furan-8,2′-oxan]-2-ol | |
| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.007.396 |
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PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C27H42O3 | |
| Molar mass | 414.630 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Diosgenin, a phytosteroid sapogenin, is the product of hydrolysis by acids, strong bases, or enzymes of saponins, extracted from the tubers of Dioscorea wild yam species, such as the Kokoro. The sugar-free (aglycone) product of such hydrolysis, diosgenin is used for the commercial synthesis of cortisone, pregnenolone, progesterone, and other steroid products.
YouTube Encyclopedic
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Diosgenin (Part 01)= Industrial Production (Isolation Method), Estimation and Utilization (Part 03)
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What does diosgenin mean?
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Lecture 44: Total synthesis of Progesterone from Diosgenin (Marker)
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Diosgenin (Part 02)= Industrial Production (Isolation Method), Estimation and Utilization (Part 04)
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Steroids – IV: Progestational Agents: Synthesis of Progesterone from Diosgenin
Transcription
Sources
It is present in detectable amounts in Costus speciosus, Smilax menispermoidea, Helicteres isora, species of Paris, Aletris, Trigonella, and Trillium, and in extractable amounts from many species of Dioscorea – D. althaeoides, D. colletti, D. composita,[1] D. floribunda, D. futschauensis, D. gracillima, D. hispida, D. hypoglauca, D. mexicana,[2] D. nipponica, D. panthaica, D. parviflora, D. septemloba, and D. zingiberensis.[3]
Industrial uses
Diosgenin is a chemical precursor for several hormones, starting with the Marker degradation process, which includes synthesis of progesterone.[4] The process was used in the early manufacturing of combined oral contraceptive pills.[5] Diosgenin in dietary supplements is not a physiological precursor to estradiol or progesterone, and the use of such products as wild yam has no hormonal activity in the human body.[6]
See also
References
- ^ "Dioscorea composita". Germplasm Resources Information Network. Agricultural Research Service, United States Department of Agriculture. Retrieved 2008-09-14.
- ^ "Dioscorea mexicana". Germplasm Resources Information Network. Agricultural Research Service, United States Department of Agriculture. Retrieved 2008-09-14.
- ^ "2950 Diosgenin". Retrieved 2007-05-29.[permanent dead link]
- ^ Marker RE, Krueger J (1940). "Sterols. CXII. Sapogenins. XLI. The Preparation of Trillin and its Conversion to Progesterone". J. Am. Chem. Soc. 62 (12): 3349–3350. doi:10.1021/ja01869a023.
- ^ Djerassi C (December 1992). "Steroid research at Syntex: "the pill" and cortisone". Steroids. 57 (12): 631–41. doi:10.1016/0039-128X(92)90016-3. PMID 1481227. S2CID 5933910.
- ^ Medigović I, Ristić N, Živanović J, Šošić-Jurjević B, Filipović B, Milošević V, Nestorović N “Diosgenin does not express estrogenic activity: a uterotrophic assay” Can J Physiol Pharmacol. 2014 Apr;92(4):292-8. doi: 10.1139/cjpp-2013-0419. Epub 2014 Feb 5. PMID: 24708211
External links
- Diosgenin at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
This page was last edited on 15 January 2024, at 13:27