Iridoid glycoside associated with immunostimmulatory and hepatoprotective activity. Key starting material for the biosynthesis of indolalkaloids. Substrate for cytochrome P450.
Product Details
| Formula: | C17H26O10 |
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| MW: | 390.4 |
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| Source: | Isolated from Cornus officinalis. |
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| CAS: | 18524-94-2 |
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| MI: | 14: 5560 |
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| Purity: | ≥98% (HPLC) |
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| Appearance: | White to off-white solid. |
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| Solubility: | Soluble in water; less soluble in 96% ethanol; sparingly soluble in 100% ethanol; insoluble in ether, petroleum ether, ethyl acetate or acetone. |
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| Shipping: | Ambient Temperature |
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| Long Term Storage: | -20°C |
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| Regulatory Status: | RUO - Research Use Only |
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Product Literature References
Indole alkaloid biosynthesis in Catharanthus roseus: new enzyme activities and identification of cytochrome P450 CYP72A1 as secologanin synthase: S. Irmler, et al.; Plant J.
24, 797 (2000),
Abstract;
Prevention of galactosamine - induced hepatic damage by the natural product loganin from the plant strychnos nux-vomica: studies on isolated hepatocytes and bile flow in rat: P.K.S. Visen, et al.; Phytother. Res. 12, 405 (1998),
Studies on the profile of immunostimulant activities of modified iridoid glycosides: V.T. Mathad, et al.; Bioorg. Med. Chem.
6, 605 (1998),
Abstract;
Alkaloid biosynthesis. 13. The structure, stereochemistry, and biosynthesis of loganin: A.R. Battersby, et al.; J. Chem. Soc.
5, 721 (1969),
Abstract;
Biosynthesis of methylcyclopentane monoterpenoids. IV. Verbenalin: A.G. Horodysky, et al.; J. Biol. Chem.
244, 3110 (1969),
Abstract;
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