| 词条 | Rosiridin |
| 释义 |
| ImageFile = Rosiridin.svg | ImageSize = 200px | ImageAlt = | IUPACName = (2R,3R,4S,5S,6R)-2-[(2E,4S)-4-Hydroxy-3,7-dimethylocta-2,6-dienoxy]-6-(hydroxymethyl)oxane-3,4,5-triol | OtherNames = |Section1={{Chembox Identifiers | CASNo = 100462-37-1 | UNII_Ref = {{fdacite|correct|FDA}} | UNII = 71AL4K0H19 | PubChem = 25068281 | SMILES = CC(=CC[C@@H](/C(=C/CO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O)/C)O)C}} |Section2={{Chembox Properties | C=16 | H=28 | O=7 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = }} |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }}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] References1. ^{{Cite journal | pmid = 18451561| year = 2008| author1 = Yoshikawa| first1 = M| title = Reinvestigation of absolute stereostructure of (-)-rosiridol: Structures of monoterpene glycosides, rosiridin, rosiridosides A, B, and C, from Rhodiola sachalinensis| journal = Chemical & Pharmaceutical Bulletin| volume = 56| issue = 5| pages = 695–700| last2 = Nakamura| first2 = S| last3 = Li| first3 = X| last4 = Matsuda| first4 = H| doi=10.1248/cpb.56.695}} {{organic-compound-stub}}2. ^{{cite journal|title=Effects of Adaptogens on the Central Nervous System and the Molecular Mechanisms Associated with Their Stress—Protective Activity|doi=10.3390/ph3010188}} 2 : Crassulaceae|Terpenoid glycosides |
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