Difference between revisions of "Spirostan"
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| − | '''Spirostan''' is a defined [[parent hydride]] in the [[nomenclature of steroids]].<ref>{{IUPAC natural products 1999}}.</ref> It is characterised by a bicyclic side chain containing a [[ketone]] [[spiro]] [[acetal]] group. In the spirostan structure, the configurations of carbons 5 and 25 | + | '''Spirostan''' is a defined [[parent hydride]] in the [[nomenclature of steroids]].<ref>{{IUPAC natural products 1999}}.</ref> It is characterised by a bicyclic side chain containing a [[ketone]] [[spiro]] [[acetal]] group. In the spirostan structure, the configurations of carbons 5 and 25 are not defined, and so must be specified for each derivative. Spirostan steroids are common as the [[Glycoside|aglycosidic]] portions of plant [[saponin]]s, and include: |
{| class="wikitable" | {| class="wikitable" | ||
Revision as of 15:37, 8 March 2010
Spirostan is a defined parent hydride in the nomenclature of steroids.[1] It is characterised by a bicyclic side chain containing a ketone spiro acetal group. In the spirostan structure, the configurations of carbons 5 and 25 are not defined, and so must be specified for each derivative. Spirostan steroids are common as the aglycosidic portions of plant saponins, and include:
| C-5 | C-25 | Other | |
|---|---|---|---|
| sarsasapogenin | β | S | 3β-OH |
| smilagenin | β | R | 3β-OH |
| tigogenin | α | R | 3β-OH |
| diosgenin | Δ5 | R | 3β-OH |
| anzurogenin-D | α | R | 3β-OH, 5α-OH, 6β-OH |
| sisalgenin | α | S | 3β-OH, C=O at C-12 |
| roscogenin | Δ5 | S | 1β-OH, 3β-OH |
References
- ↑ Revised Section F: Natural Products and Related Compounds (IUPAC Recommendations 1999). Pure Appl. Chem., 71 (4), 587–643. DOI: 10.1351/pac199971040587.
