CAS: 18749-71-8; Sitoindoside I

该化合物是一种化学化合物,被归类为一种以表面活性特性而闻名的胶质,主要来源于植物物种* Orenania somnifera*, 通常称为hwagandha;该化合物的特点是结构复杂,通常包括一种与糖糖糖相连的抗血清激素;Sitoindoside I因其潜在的药理效应而得到承认,包括抗炎,抗氧化剂和适应性特性,因此对传统医药和现代草药补充物感兴趣;其生物活性主要归功于其调节各种生物途径的能力,有助于抗压力和总体健康惠益;此外,Satoindoside I可以展示肝炎活动,这是该类许多化合物的特征之一.由于其自然起源和潜在健康惠益,研究继续探索其在治疗环境中的应用,尽管需要进一步研究,以充分理解其机制和效率.

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    上下游产品

    Daucosterol n-hexadecanoyl chloride β-sitosterol 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromidehexadecanoic acid methyl ester 1-hexadecylcarboxylic acid β-sitosterol

    合成工艺路线路线简述

      📜豆甾醇置于吡啶,Magnesium Sulfate,Silver(L) Oxide体系中,用 乙醚,苯 用作溶剂,化学反应 72.0H,反应生成Sitoindoside I; (6'-O-棕榈酰基)-3Beta-D-吡喃葡萄糖基谷甾醇
      参考文献:Suppressors Of Cancer Cell Proliferation From Fig (Ficus Carica) Resin: Isolation And Structure Elucidation
      标题:Suppressors Of Cancer Cell Proliferation From Fig (Ficus Carica) Resin: Isolation And Structure Elucidation
      摘要:A Mixture Of 6-O-Acyl-Beta-D-Glucosyl-Beta-Sitosterols,The Acyl Moeity Being Primarily Palmitoyl And Linoleyl With Minor Amounts Of Stearyl And Oleyl,Has Been Isolated As A Potent Cytotoxic Agent From Fig (Ficus Carica) Latex And Soybeans. Identity Was Established By Spectroscopic Methods (NMR,Ms) And Confirmed By Chemical Synthesis. Both The Natural And The Synthetic Compounds Showed In Vitro Inhibitory Effects On Proliferation Of Various Cancer Cell Lines.
      Doi:10.1021/np000592Z

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      ✅ COA系统入驻 | 共享模式

      合成参考文献


      参考文献:10.1016/j.phytochem.2004.08.002
      摘要:Ahmed AA, Hussein TA, Mahmoud AA, Farag MA, Paré PW, Wojcińska M, Karchesy J, Mabry TJ. Nor-ent-kaurane diterpenes and hydroxylactones from Antennaria geyeri and Anaphalis margaritacea. Phytochemistry. 2004 Sep;65(18):2539–43. doi: 10.1016/j.phytochem.2004.08.002.
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