Rosiridin
Rosiridin has been the subject of interest and debate for a long time. Its importance lies in the impact it has on different aspects of daily life. In this article, we will explore in depth what Rosiridin means, its history, its current relevance and its future projection. Additionally, we will analyze how Rosiridin affects different sectors of society and how it has evolved over time. With a critical and objective perspective, this article seeks to provide a comprehensive vision of Rosiridin and its influence in today's world.
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| Names | |
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| IUPAC name
(2R,3R,4S,5S,6R)-2-{oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C16H28O7 | |
| Molar mass | 332.393 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
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Rosiridin is a chemical compound that has been isolated from Rhodiola sachalinensis.[1] Rosiridin can inhibit monoamine oxidases A and B, possibly meaning that the compound could help in the treatment of depression and senile dementia.[2][3]
References
- ^ Yoshikawa, Masayuki; Nakamura, Seikou; Li, Xuezheng; Matsuda, Hisashi (2008). "Reinvestigation of absolute stereostructure of (−)-rosiridol: Structures of monoterpene glycosides, rosiridin, rosiridosides A, B, and C, from Rhodiola sachalinesnsis". Chemical and Pharmaceutical Bulletin. 56 (5): 695–700. doi:10.1248/cpb.56.695. PMID 18451561.
- ^ Panossian, Alexander; Wikman, Georg (2010). "Effects of adaptogens on the central nervous system and the molecular mechanisms associated with their stress-protective activity". Pharmaceuticals. 3 (1): 188–224. doi:10.3390/ph3010188. PMC 3991026. PMID 27713248.
- ^ van Diermen, Daphne; Marston, Andrew; Bravo, Juan; Reist, Marianne; Carrupt, Pierre-Alain; Hostettmann, Kurt (2009-03-18). "Monoamine oxidase inhibition by Rhodiola rosea L. roots". Journal of Ethnopharmacology. 122 (2): 397–401. doi:10.1016/j.jep.2009.01.007. ISSN 0378-8741.
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