CAS: 60820-94-2; (2R,4Ar,6As,6Br,9R,10R,11S,12Ar,12Br,14Br)-11-Hydroxy-9-(Hydroxymethyl)-2-(Methoxycarbonyl)-2,6A,6B,9,12A-Pentamethyl-10-(((2S,3R,4S,5R)-3,4,5-Trihydroxytetrahydro-2H-Pyran-2-yl)Oxy)-1,3,4,5,6,6A,6B,7,8,8A,9,10,11,12,12A,12B,13,14B-Octadecahydropicene-4A(2H)-Carboxylic Acid

该化合物是一种主要来自各种植物来源的沙邦素化合物,特别是产卵* 的植物来源,其特点是其甘蓝素结构,通常由糖浆组成,与类固醇或丙烯酮相关联,这种复合物呈现出一系列生物活动,包括潜在的抗炎,抗氧化剂和抗癌特性,从而引起药理研究的兴趣. 乙类动物群也因其与细胞膜相互作用的能力而闻名于世,这可能有助于其生物效应. 就溶液而言,如埃斯库伦托塞德B类的沙邦素一般在水中溶解,可形成稳定的泡沫,这种特征经常在各种应用中被利用.其安全特征和潜在的治疗用途仍在调查之中,强调需要进一步研究,以充分了解其药用的行动和功效机制.

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上下游产品

Oleanolic acid 4)-β-D-xylopyranosyl)-phytolaccagenin3-O-(β-D-glucopyranosyl-(1-4)-β-D-xylopyranosyl)-phytolaccageninL-arabinose

合成工艺路线路线简述

    📜商陆皂苷甲置于β-D-Glucosidase From Snailase,Calcium Chloride体系中,用 Aq. Buffer 作为反应溶剂,化学反应 0.17H,反应生成 商陆皂甙乙;商陆皂苷乙;美商陆皂苷b
    参考文献:Efficient Enzymatic Preparation Of Esculentoside B Following Condition Optimization By Response Surface Methodology
    标题:Efficient Enzymatic Preparation Of Esculentoside B Following Condition Optimization By Response Surface Methodology
    摘要:Esculentoside B (Esb,Also Named Phytolaccagenin 3-O-Beta-D-Xylopyranoside),A Pentacyclic Triterpene Isolated From Herbal Medicine Radix Phytolaccae,Has Been Found To Possess Multiple Pharmacological Activities. Nonetheless,The Low Content In Nature And The Difficulties In The Total Synthesis Of Esb Strongly Limit Its Extensive Investigations And Further Development As A Drug Candidate. This Study Aims To Provide A Practical Method For Highly Efficient Preparation Of Esb Using Esculentoside A (Esa,Phytolaccagenin 3-Beta-D-Glucopyranosyl (1-> 4)-Beta-D-Xylopyranoside) As The Starting Material. Beta-D-Glucosidase From Snailase Was Used To Catalyze The Formation Of Esb,And The Product Was Then Purified And Fully Characterized By Both Hrms And NMR. To Prepare Esb In A More Cost-Effective Way,Response Surface Methodology (Rsm) Was Used To Explore The Potential Effects Of The Reaction Conditions (Such As Reaction Temperature,Ph,Enzyme Load,And Reaction Time) On The Conversion Rates Of Esa. The Highest Esb Yield Of 0.66 Mg/ml Was Obtained Experimentally Under Optimized Conditions As Follows: Temperature 48.28 Degrees C,Ph 6.4,Enzyme Load 4.43%,And Reaction Time 2.73 H. This Result Agreed Well With The Predicted Yield Of 0.68 Mg/ml By Rsm. The Enzymatic Kinetics Of This Biotransformation Was Characterized At The Optimum Ph And Temperature. The S-50 Value Was Evaluated As 167.4 Mu M,While The Vmax Value Was 345.6 Nmol/min/mg. In Summary,This Study Provided A Mild And Practical Method For The Highly Efficient Preparation Of Esb From Esa,Which Held Great Promise For Large Scale Production Of Esb. (C) 2016 Elsevier B.V. All Rights Reserved.
    DOI:10.1016/j.Molcatb.2016.04.013

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:Saengyak Hakhoechi. Journal of the Society of Pharmacognosy., 10(73), 1979
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