CAS: 121591-98-8; Xyloglucan Heptasaccharide

该化合物是一种主要因其在生物化学和分子生物学领域应用而得到承认的合成化合物,是一种在各种生化过程中,特别是在细胞信号和相互作用研究中发挥重要作用的甘蓝蛋白. XXXG经常用于植物生物学研究,特别是在植物生长和发育方面,因为它能够影响细胞墙特性和植物激素信号路径.该化合物的特点是能够调节某些酶和受体的活动,使其成为实验环境中的宝贵工具.此外,其稳定性和水溶性在水溶液中的溶解性促进了实验室实验的利用.与许多化学物质一样,在处理XXXG时,应当注意安全防范措施,包括使用适当的个人防护设备,遵守安全数据表准则.

结构式图片

合成工艺路线路线简述

    专利信息


    专利号:US-2024024489-A1
    优先权日:2020-11-20
    标 题:Protected disaccharides, their process of preparation and their use in the synthesis of zwitterionic oligosaccharides, and conjugates thereof
    发明人:MULARD LAURENCE; DHARA DEBASHIS; PFISTER HELENE; PAOLETTI JULIE; PHALIPON ARMELLE; GUERREIRO-INVERNO CATHERINE
    权利人:PASTEUR INSTITUT
    摘要:The present invention provides zwitterionic oligosaccharides, in particular fragments of the surface polysaccharides from Shigella sonnei and Shigella sonnei conjugates comprising them. The present invention also provides protected disaccharides, their process of preparation and their use in the synthesis of zwitterionic oligosaccharides, and conjugates thereof, the disaccharide repeating unit of Shigella sonnei being: (I)

    专利号:US-5808019-A
    优先权日:1994-12-19
    标题 :Intermediate compounds for the synthesis of glycolipids
    发明人:HASEGAWA AKIRA; KISO MAKOTO; ISOGAI YUKIHIRO; KITAMURA SEIICHI; UEDA HIROSHI
    权利人:TOA BOSHOKU KABUSHIKI KAISHA
    摘要:The invention provides important intermediate compounds for the synthesis of acidic glycolipids which are identical with the glycolipid antigens isolated from the acidic glycolipid fractions of peripheral nerve and embryonic central nervous system and preparation methods thereof. By the adoption of the present intermediate compounds, sulfation of 3-hydroxyl group of end glucuronic acid portion of the acidic glycolipid can be quite easily carried out and total synthetic yield be greatly improved.

    专利号:US-7485718-B2
    优先权日:2005-06-16
    标题:Chemical synthesis of low molecular weight polyglucosamines and polygalactosamines
    发明人:SABESAN SUBRAMANIAM
    权利人:DU PONT
    摘要:A process for the synthesis of beta linked low molecular weight polymers of galactosamine and glucosamine has been developed. Through the use of high amounts of activating agents, efficient coupling of stable monomers is achieved. Using this process, chain extension is through the addition of single monomers, providing populations of single chain length polyhexosamines.

    专利号:EP-3835306-A1
    优先权日:2019-12-13
    标题:Microwave-assisted method for synthesis of oligo- and polysaccharides on solid phase
    权利人:MAX PLANCK GESELLSCHAFT
    摘要:The present invention relates to a method for synthesizing oligo- and polysaccharides using microwave radiation, in particular to a method and a device for automated synthesis of oligo- and polysaccharides.

    专利号:US-11306157-B2
    优先权日:2018-12-21
    标 题:Expedient synthesis of core disaccharide building blocks from natural polysaccharides for heparan sulfate oligosaccharide assembly
    发明人:HSIEH-WILSON LINDA C; PAWAR NITIN J; WANG LEI
    权利人:CALIFORNIA INST OF TECHN
    摘要:Methods for the preparation of oligosaccharide products from polysaccharide starting materials are disclosed. The methods include: hydrolyzing a glucosamine-containing polysaccharide starting material, such as heparin or heparosan, under conditions sufficient to form an oligosaccharide intermediate (e.g., a GlcN-IdoA disaccharide intermediate or a GlcA-GlcN disaccharide intermediate), and converting the oligosaccharide intermediate to the oligosaccharide product. Conversion of the oligosaccharide intermediates to the oligosaccharide products may include one or more esterification, acylation, epimerization, protection, and deprotection steps. Preparation of higher-order oligomers is described, as well as methods for selective oligosaccharide sulfation.

    专利号:WO-9222662-A1
    优先权日:1991-06-10
    标 题:Methods for the synthesis of monofucosylated oligosaccharides terminating in di-n-acetyllactosaminyl structures
    发明人:VENOT ANDRE P; KASHEM MOHAMMED A; SMITH RICHARD H
    权利人:ALBERTA RES COUNCIL
    摘要:Disclosed are methods for the preparation of monofucosylated and sialylated derivatives of the compound $g(b)Gal(1-4)$g(b)GlcNAc(1-3)$g(b)Gal(1-4)$g(b)GlcNAc-R. In particular, the methods of this invention provide for a multi-step synthesis wherein selective monofucosylation is accomplished on the 3-hydroxy group on only one of the GlcNAc units found in the $g(b)Gal(1-4)$g(b)GlcNAc(1-3)$g(b)Gal(1-4)$g(b)GlcNAc-R compound. In this step, monofucosylation is achieved by use of the $g(a)(1-3)fucosyltransferase.
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