CAS: 84380-10-9; (1S,2R)-1-((2R,3R,4S,6S)-3-Acetamido-4-Acetoxy-6-Hydroxy-6-(Methoxycarbonyl)Tetrahydro-2H-Pyran-2-yl)Propane-1,2,3-Triyl Triacetate

该化合物是一种复杂的碳水化合物衍生物,其特点是多乙基组,可提高其溶解性和稳定性.该化合物的特点是一种非氨酸结构,特别是一种3,5-dideoxy糖,在生物系统,特别是在石丙酮和甘油合成中具有重大意义. 乙基氨基氨基氨组的存在表明潜在的生物活动,可能影响与蛋白质或细胞膜的相互作用.四氧-O-辛基磺酸酶表明,所有氢氟基化合物都是乙基酰,可影响化合物在生物化学途径中的再活动与互动.该物质可能是一种合成中间或一种工具,用于研究碳水化合物-丙基化合物-丙基化学的化学特性.

结构式图片

上下游产品

CAS号108-24-7 乙酸酐 | CAS号67670-69-3 N-乙酰基-2-氯-2-脱氧神... | CAS号132883-18-2 D-glycero-D-gal... | CAS号19342-33-7 (2S,4S,5S,6R)-5... | CAS号333-20-0 硫氰酸钾 | CAS号75-36-5 乙酰氯 | CAS号73960-72-2 (2R,3R,4S)-3-乙酰... | CAS号3063-71-6 唾液

合成工艺路线路线简述

    📜N-Acetyl Neuraminic Acid置于dowex [50W-X8 (H+)]体系中,化学反应 32.0H,反应生成 4,7,8,9-四-O-乙酰基-N-乙酰神经氨酸甲酯
    参考文献:Cmp-唾液酸衍生物的化学合成和酶促测试
    标题:Cmp-唾液酸衍生物的化学合成和酶促测试
    摘要:唾液酸修饰:Cyclo Sal核苷酸用于制备单磷酸连接的糖核苷酸,例如tmp-β-Gal和cmp-N-乙酰基神经氨酸以及四种唾液酸衍生物,它们的氨基官能团具有不同的修饰.在细菌多唾液酸转移酶催化的聚合反应中研究了cmp-唾液酸衍生物.
    DOI:10.1002/cbic.201200471

    海关参考信息

    专利信息


    专利号:US-6319695-B1
    优先权日:1991-10-15
    标 题:Production of fucosylated carbohydrates by enzymatic fucosylation synthesis of sugar nucleotides; and in situ regeneration of GDP-fucose
    发明人:WONG CHI-HUEY; ICHIKAWA YOSHITAKA; SHEN GWO-JENN; LIU KUN-CHIN
    权利人:SCRIPPS RES INSITUTE
    摘要:This invention contemplates improved methods of enzymatic production of carbohydrates especially fucosylated carbohydrates. Improved syntheses of glycosyl 1- or 2-phosphates using both chemical and enzymatic means are also contemplated. The phosphorylated glycosides are then used to produce sugar nucleotides that are in turn used as donor sugars for glycosylation of acceptor carbohydrates. Especially preferred herein is the use of a disclosed method for fucosylation.

    专利号:EP-0642526-B1
    优先权日:1991-10-15
    标题:Production of fucosylated carbohydrates by enzymatic fucosylation synthesis of sugar nucleotides; and in situ regeneration of gdp-fucose

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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

    主要参考文献

    参考标题:Large‐scale Synthesis Of Per‐O‐acetylated Saccharides And Their Sequential Transformation To Glycosyl Bromides And Thioglycosides
    作者:Li‐cheng Huang,Pi‐hui Liang,Ching‐yang Liu,Chun‐cheng Lin |发布日期:2006.6
    摘要:This Work Describes A Large‐scale Synthesis Of Per‐o‐acetylated Mono‐ And Disaccharides Using A Stoichiometric Amount Of Acetic Anhydride In The Presence Of Liclo4 Under Solvent‐free Conditions. The Peracetylated Saccharides Underwent Subsequent Anomeric Bromination And Thioglycosidation In One‐pot To Yield Synthetically Valuable Building Blocks.

    合成参考文献


    摘要:Stankevič, M.; Pietrusiewicz, K. M., Science of Synthesis, (2009) 42, 295.
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