CAS: 36190-95-1; 3'-O-Methylorobol

该化合物是一种混合物混合物,是苯丙胺结构,代之以有助于其化学反应和生物活动的氢氧基和甲基氧基组群;多个氢氧基体组的存在增强了其作为抗氧化剂的潜力,使其得以对自由基进行抗毒和减轻氧化性压力;此外,甲基氧基组可以影响其溶解性和与生物系统的互动;该化合物经常因其药性特性进行研究,包括抗炎,抗微生物和抗癌活动;其结构复杂性允许与生物目标进行各种互动,使其成为医药化学和天然产品研究的一个对象;

结构式图片

上下游产品

5,7-Dihydroxy-3-(4-hydroxy-phenyl)-chromen-4-on homoeriodictyol orobol

合成工艺路线路线简述

    📜高圣草酚置于nadph Disodium Salt,口服葡萄糖体系中,用 二甲基亚砜 用作溶剂,化学反应 72.0H,反应生成3'-O-甲基香豌豆苷元
    参考文献:A Versatile Microbial System For Biosynthesis Of Novel Polyphenols With Altered Estrogen Receptor Binding Activity
    标题:A Versatile Microbial System For Biosynthesis Of Novel Polyphenols With Altered Estrogen Receptor Binding Activity
    摘要:Isoflavonoids Possess Enormous Potential For Human Health With Potential Impact On Heart Disease And Cancer,And Some Display Striking Affinities For Steroid Receptors. Synthesized Primarily By Legumes,Isoflavonoids Are Present In Low And Variable Abundance Within Complex Mixtures,Complicating Efforts To Assess Their Clinical Potential. To Satisfy The Need For Controlled,Efficient,And Flexible Biosynthesis Of Isoflavonoids,A Three-Enzyme System Has Been Constructed In Yeast That Can Convert Natural And Synthetic Flavanones Into Their Corresponding Isoflavones In Practical Quantities. Based On The Determination Of The Substrate Requirements Of Isoflavone Synthase,A Series Of Natural And Nonnatural Isoflavones Were Prepared And Their Binding Affinities For The Human Estrogen Receptors (Er Alpha And Er Beta) Were Determined. Structure Activity Relationships Are Suggested Based On Changes To Binding Affinities Related To Small Variations On The Isoflavone Structure.
    Doi:10.1016/j.Chembiol.2010.03.010

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    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1016/s0031-9422(00)81244-3
    摘要:McCormick S, Robson K, Bohm B. Flavonoids of Wyethia angustifolia and W. helenioides. Phytochemistry. 1986 Jan;25(7):1723–6. doi: 10.1016/s0031-9422(00)81244-3.
    参考文献:10.1016/s0031-9422(00)84936-5
    摘要:Tahara S, Ingham JL, Nakahara S, Mizutani J, Harborne JB. Fungitoxic dihydrofuranoisoflavones and related compounds in white lupin, Lupinus albus. Phytochemistry. 1984 Aug;23(9):1889–900. doi: 10.1016/s0031-9422(00)84936-5.
    参考文献:10.1016/s0031-9422(00)91408-0
    摘要:Let̀e de Almeida ME, Gottlieb OR. Iso- and neo-flavonoids from Dalbergia inundata. Phytochemistry. 1974 Apr;13(4):751–2. doi: 10.1016/s0031-9422(00)91408-0.
    参考文献:10.1016/0031-9422(91)84117-b
    摘要:Hanawa F, Tahara S, Mizutani J. Isoflavonoids produced by Iris pseudacorus leaves treated with cupric chloride. Phytochemistry. 1991 Jan;30(1):157–63. doi: 10.1016/0031-9422(91)84117-b.
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