CAS: 88515-58-6; (2S,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Tetrahydro-2H-Pyran-2-Yl (1R,2R,4As,6As,6Br,8Ar,10R,11R,12Ar,12Br,14Bs)-1,10,11-Trihydroxy-1,2,6A,6B,9,9,12A-Heptamethyl-1,3,4,5,6,6A,6B,7,8,8A,9,10,11,12,12A,12B,13,14B-Octadecahydropicene-4A(2H)-Carboxylate

该化合物是罗萨凯家族的植物来源.典型的罗萨多罗展示抗氧化剂特性,有助于其潜在的健康惠益,包括防炎和抗癌效应.该化合物由于有能力收集自由基,常常因其在传统医学及其在食品和化妆品工业中的应用中所起的作用而得到研究.此外,罗萨多伦可能会影响各种生物途径,使其成为药理研究的兴趣对象.其溶性性和稳定性可因溶剂和环境条件而不同而不同,而这些条件对制剂的应用至关重要.

结构式图片

上下游产品

Potentillanoside C 1345828-74-1
Potentillanoside A 1309589-79-4

合成工艺路线路线简述

  • 1345828-74-1 = 88515-58-6
    反应条件:1.1 Reagents: Sodium Methoxide Solvents: Methanol; 1 H,Rt
    标题:Hepatoprotective Triterpenes From Traditional Tibetan Medicine Potentilla Anserina
    作者:Morikawa,Toshio; Et Al
    参考文献:Phytochemistry (Elsevier) 日期:2014 卷标:102 页码:169-181]

    1309589-79-4 = 88515-58-6 + 95298-47-8
    反应条件:1.1 Reagents: Sodium Borohydride Solvents: Methanol; 1 H,0 °C1.2 Reagents: Acetone; 0 °C
    标题:Hepatoprotective Triterpenes From Traditional Tibetan Medicine Potentilla Anserina
    作者:Morikawa,Toshio; Ninomiya,Kiyofumi; Imura,Katsuya; Yamaguchi,Takahiro; Akagi,Yoshinori; Et Al
    参考文献:Phytochemistry (Elsevier) 日期:2014 卷标:102 页码:169-181]

    921-60-8 + 508-02-1 = 88515-58-6 + 31297-79-7 + 14162-53-9 + 78454-20-3 + 3391-80-8 + 95298-47-8
    反应条件:1.1 4 D
    标题:Biotransformation Of Oleanolic Acid By Alternaria Longipes And Penicillium Adametzi
    作者:Liu,Dai-Lin; Liu,Ying; Qiu,Feng; Gao,Ying; Zhang,Jing-Ze
    参考文献:Journal Of Asian Natural Products Research 日期:2011 卷标:13(2) 页码:160-167
📜Potentillanoside C置于sodium Methylate体系中,用 甲醇 作为反应溶剂,化学反应 1.0H,以97.2%的收率获得产物1-O-[(2Beta,3Alpha,5Xi,9Beta,18Alpha)-2,3,19-三羟基-28-氧代乌苏-12-烯-28-基]-Beta-D-吡喃葡萄糖
参考文献:Hepatoprotective Triterpenes From Traditional Tibetan Medicine Potentilla Anserina
标题:Hepatoprotective Triterpenes From Traditional Tibetan Medicine Potentilla Anserina
摘要:A Methanol Extract From The Tuberous Roots Of Potentilla Anserina (Rosaceae) Exhibited Hepatoprotective Effects Against D-Galactosamine (D-Galn)/lipopolysaccharide-Induced Liver Injuries In Mice. Six Triterpene 28-O-Monoglucopyranosyl Esters,Potentillanosides A-F,Were Isolated From The Extract Along With 32 Known Compounds,Including 15 Triterpenes. The Structures Of Potentillanosides A-F Were Determined On The Basis Of Spectroscopic Properties And Chemical Evidence. Four Ursane-Type Triterpene 28-O-Monoglycosyl Esters,Potentillanoside A (Ic50 = 46.7 Mu M),28-O-Beta-D-Glucopyranosyl Pomolic Acid (Ic50 = 9.5-Mu M),Rosamutin (Ic50 = 35.5 Mu M),And Kaji-Ichigoside F1 (Ic50 = 14.1 Mu M),Inhibited D-Galn-Induced Cytotoxicity In Primary Cultured Mouse Hepatocytes. Among These Four Triterpenes,Potentillanoside A,Rosamutin,And Kaji-Ichigoside F1 Exhibited In Vivo Hepatoprotective Effects At Doses Of 50-100 Mg/kg,P.O. The Mode Of Action Was Ascribable To The Reduction In Cytotoxicity Caused By D-Galn. (C) 2014 Elsevier Ltd. All Rights Reserved.
DOI:10.1016/j.Phytochem.2014.03.002

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✅ COA系统入驻 | 共享模式

主要参考文献


1: Cheol Park J, Chul Kim S, Moon Hur J, Choi SH, Yeon Lee K, Won Choi J. Anti-hepatotoxic effects of Rosa rugosa root and its compound, rosamultin, in rats intoxicated with bromobenzene. J Med Food. 2004 Winter;7(4):436-41. German. doi: 10.4268/cjcmm20160316. Chinese. Chinese. doi: 10.1016/j.intimp.2011.01.002. Epub 2011 Jan 13. Chinese.

合成参考文献


参考文献:10.1002/(sici)1099-1573(199906)13:4<323::aid-ptr448>3.0.co;2-c|10.1002/(sici)1099-1573(199906)13:4<323::aid-ptr448>3.3.co;2-3
摘要:Simões CM, Amoros M, Girre L. Mechanism of antiviral activity of triterpenoid saponins. Phytother Res. 1999 Jun;13(4):323–8. doi: 10.1002/(sici)1099-1573(199906)13:4<323::aid-ptr448>3.0.co;2-c.
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