CAS: 20818-25-1; (2S,3R,4S,5S,6R)-2-(4-Aminophenoxy)-6-(Hydroxymethyl)Tetrahydro-2H-Pyran-3,4,5-Triol

该化合物是一种胶质派衍生物,通常用作酶学分析的基质,特别是用于β-glucosidase 活动研究,其结构具有与4-氨基苯组相连的β-D-glucopromalosy mothy mothy moth yculative;该化合物在生物化学研究中具有高度的特性和敏感性,便于对酶动因进行准确的量化,因此受到重视;在标准实验室条件下的稳定性和水溶性进一步提高了其在体外应用中的实用性;此外,释放的4-氨基苯酚产品可以很容易地测量光谱,从而在酶学和分子生物学中成为诊断和研究目的的可靠选择.

结构式图片

相似化合物

5094-33-7 34213-86-0 35599-02-1

上下游产品

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合成工艺路线路线简述

    📜4-硝基苯-β-D-吡喃葡萄糖苷置于palladium 10% On Activated Carbon,氢气体系中,用 甲醇 用作溶剂,化学反应 7.0H,以97%的收率获得七烷基-2-乙酰氨基-2-脱氧-β-D-吡喃葡糖苷
    参考文献:Yariv试剂合成和纯化的改进方案
    标题:Yariv试剂合成和纯化的改进方案
    摘要:Yariv试剂是广泛用于植物生物学的糖缀合物tris-Azo染料.这些试剂通过间苯三酚和对重氮苯基糖苷之间的重氮偶合来合成.尽管可以合成,但尚未报道用于获得纯yariv试剂的明确定义的方案及其完整的化合物表征数据.我们在这里报告了用于合成,纯化和表征一组六种yariv试剂的优化方案,并提出了对其他糖缀合物的纯化和表征也可能有价值的方法.
    Doi:10.1021/acs.Joc.0C01812

    海关参考信息

    专利信息


    专利号:US-2003138880-A1
    优先权日:2001-08-24
    标 题:Solid-phase synthesis of oligosaccharides and glycopeptides using glycosynthases
    发明人:WITHERS STEPHEN G; JENSEN KNUD J; PETERSEN LARS; TOLBORG JAKOB L
    权利人:UNIV BRITISH COLUMBIA
    摘要:The present invention provides materials and methods for the solid-phase synthesis of oligosaccharides and glycopeptides. Such materials and methods include mutant glycosidase enzymes, or “glycosynthases,â€? chemically-derivatized acceptor molecules, and specific solid support matrices.

    专利号:US-8273403-B2
    优先权日:2002-05-10
    标题 :Generation of surface coating diversity
    发明人:BARDEN MICHAEL C; KAMBOURIS PETER A
    权利人:BARDEN MICHAEL C; KAMBOURIS PETER A; BIO LAYER PTY LTD
    摘要:This invention relates to a surface discovery system and high-throughput combinatorial synthesis methods for generating large numbers of diverse surface coatings on solid substrates. The system is built upon a synthon which comprises at least three elements: a chemical backbone coating on the solid substrate that comprises a copolymer (B) of at least one passive constituent (P) and at least one active constituent (A); a spacer unit (S) separating the backbone from a functional group; and a functional group (F). The methods comprise the following steps: 1) selecting a plurality of synthons so that each synthon has at least two points of diversity selected from P, A, S and F; 2) applying copolymer B onto a substrate; and 3) attaching a combination of S and F to constituent A of copolymer B. Steps 2) and 3) are performed such that different synthons are generated on localized regions of the substrate.

    专利号:WO-03018605-A2
    优先权日:2001-08-24
    标 题:Solid-phase synthesis of oligosaccharides and glycopeptides using glycosynthases

    供应商参考报价(招募中)

    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:Microwave-Assisted Facile Synthesis Of Red-Shifted Azobenzene Glycoconjugates
    作者:Vivek Poonthiyil,Franziska Reise,Guillaume Despras,Thisbe K. Lindhorst |发布日期:2018.12.6
    摘要:The First Red‐shifted Photoswitchable Glycoconjugates Are Reported. Microwave‐assisted Late‐stage C-H Chlorination Was Employed To Achieve Tetra‐ortho‐chlorinated Azobenzene Glycoconjugates. To Investigate Orientational Control In Carbohydrate Recognition, A Red‐shifted Glycoazobenzene Alkanethioacetate Was Also Prepared. Scope And Limitations Of Late‐stage C-H Chlorination Of Sugar Derivatives Is

    合成参考文献


    参考文献:10.1111/j.1471-4159.1988.tb10607.x
    摘要:Naoi M, Shibahara K, Suzuki H, Nagatsu T. Specific binding of glycosylated beta-galactosidase to rat clonal pheochromocytoma PC12h cells: effects of nerve growth factor and gangliosides. J Neurochem. 1988 Apr;50(4):1297–301. doi: 10.1111/j.1471-4159.1988.tb10607.x.
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