CAS: 3615-37-0; (2R,3S,4S,5R)-2,3,4,5-Tetrahydroxyhexanal

该化合物是一种自然形成的单沙律,具体地说是一种在各种生物过程中发挥重要作用的单沙律,在各种生物过程中,D-manose是一种显微粒,其特点是六碳结构,其中包括C-6位置的氢氧化硫组.D-foose通常在L-form 自然中找到,但D-fose在某些甘蓝蛋白和甘蓝脂中很重要.D-formose在水中溶解并表现出甜味.D-fooce涉及细胞识别和信号,特别是在免疫反应和细胞粘合方面.D-foose的存在对于富含氟化甘油的合成至关重要,对各种生理功能都很重要.D-foose还研究其潜在的治疗用途,包括其在癌症生物学和生物前的作用.D-foose可以从各种自然来源获得,包括海藻和某些细菌,并经常用于研究和生物技术应用.

结构式图片

相似化合物

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合成工艺路线路线简述

    6-脱氧-6-碘-1,2:3,4-二-O-异亚丙基-α-D-半乳糖吡喃糖苷置于palladium On Activated Charcoal 氢气,溶剂黄146,三乙胺体系中,化学反应生成 D-岩藻糖
    参考文献:沙门氏菌血清群b的抗原决定簇.用作人工抗原的三糖苷的合成
    标题:沙门氏菌血清群b的抗原决定簇.用作人工抗原的三糖苷的合成
    摘要:已经投入了大量的努力来合成与沙门氏菌血清群a,B和d的o-抗原有关的抗原决定簇.迄今为止,在o特异性链的二糖和高阶线性低聚糖半抗原的合成中出现了一些报告v.另外,我们最近报道了沙门氏菌血清群a和d的两支三糖半抗原的合成,这些半抗原适当地衍生化以允许共价结合到蛋白质,细胞表面和免疫吸收支持物上.可以预期,该三糖序列,即ad-Gal-(1 + 2)-[3,6-二脱氧-Cu-Dhexopyranosyl-(1 + 3)]-Cy_d-M An将与显性3,6-二脱氧己糖在沙门氏菌血清学中的作用,由于吡喃糖基取代基在邻位氧原子(o-2和o-3)9Jo处具有相当高的构象刚度.现在,我们报告了与沙门氏菌血清群b的0抗原决定簇相对应的支链三糖结构的合成.此研究程序中合成的化合物很有意义,因为它们可用于推断o抗原构象9Jo的模型,协助从体细胞融合实验中选择杂交骨髓瘤抗体",并研究沙门氏菌抗原与单克隆抗体的相互
    DOI:10.1016/0008-6215(84)85211-8

    海关参考信息

    专利信息


    专利号:US-12188072-B2
    优先权日:2018-03-19
    标题 :Compositions and methods for rapid in vitro synthesis of bioconjugate vaccines in vitro via production and N-glycosylation of protein carriers in detoxified prokaryotic cell lysates
    发明人:JEWETT MICHAEL CHRISTOPHER; STARK JESSICA CAROL; DELISA MATTHEW P; JAROENTOMEECHAI THAPAKORN
    权利人:UNIV NORTHWESTERN; UNIV CORNELL
    摘要:Disclosed are methods, systems, components, and compositions for cell-free synthesis of glycosylated carrier proteins. The glycosylated carrier proteins may be utilized in vaccines, including anti-bacterial vaccines. The glycosylated carrier proteins may include a bacterial polysaccharide conjugated to a carrier, which may be utilized to generate an immune response in an immunized host against the polysaccharide conjugated to the carrier. The glycosylated carrier proteins may be synthesized in cell-free glycoprotein synthesis (CFGpS) systems using prokaryote cell lysates that are enriched in components for glycoprotein synthesis such as oligosaccharyltransferases (OSTs) and lipid-linked oligosaccharides (LLOs) including OSTs and LLOs associated with synthesis of bacterial O antigens.

    专利号:US-12365930-B2
    优先权日:2016-07-14
    标题:Method for rapid in vitro synthesis of glycoproteins via recombinant production of N-glycosylated proteins in prokaryotic cell lysates
    发明人:JEWETT MICHAEL CHRISTOPHER; STARK JESSICA CAROL; DELISA MATTHEW P; JAROENTOMEECHAI THAPAKORN
    权利人:UNIV NORTHWESTERN; UNIV CORNELL
    摘要:Disclosed are methods, systems, components, and compositions for cell-free synthesis of glycosylated proteins. The glycosylated proteins may be utilized in vaccines, including anti-bacterial vaccines. The glycosylated proteins may include a bacterial polysaccharide conjugated to a carrier, which may be utilized to generate an immune response in an immunized host against the polysaccharide conjugated to the carrier. The glycosylated proteins may be synthesized in cell-free glycoprotein synthesis (CFGpS) systems using prokaryote cell lysates that are enriched in components for glycoprotein synthesis such as oligosaccharyltransferases (OSTs) and lipid-linked oligosaccharides (LLOs) including OSTs and LLOs associated with synthesis of bacterial O antigens.

    专利号:US-2004266699-A1
    优先权日:2001-10-04
    标 题 :Flavonoid compounds capable of modifying the dynamic and/or physical state of biological membranes and to stimulate the endogenous synthesis of stress proteins in eukaryotic cells, relative synthesis and their use
    发明人:PORTA AMALIA
    摘要:The invention relates to flavonoids compounds of formula (I) and (II) capable of modifying the dynamic and/or physical state of biological membranes and to stimulate the endogenous synthesis of stress proteins in eukaryotic cells. Such compounds are molecules of plant origin or synthetic. The invention also describes a method to identify, purify and chemically synthesize such flavonoid compounds and test their efficacy through their capacity to stimulate the transcription of stress genes and as a consequence, to interact with biological membranes with alteration of their relative physical state. Such compounds and corresponding pharmaceutically acceptable derivatives and/or salts have applications in the areas of pharmaceuticals, more specifically in cosmetics and dermatology, for all those afections related to an alteration of the expression of stress genes.

    专利号:US-2022395800-A1
    优先权日:2019-11-04
    标题:Device for automated synthesis of oligo- and polysaccharides
    发明人:SEEBERGER PETER H; DANGLAD FLORES JOSE; LE MAI HOANG KIM; PARDO VARGAS ALONSO; SLETTEN ERIC; SALWICZEK MARIO
    权利人:MAX PLANCK GESELLSCHAT ZU RFERDERUNG DER WSS E V; GlycoUniverse GmbH & Co KG&A
    摘要:The present invention generally relates to automated synthesis technology, and more particularly, to a device and method for automated synthesis of oligo- and polysaccharides on a solid support. In particular the present invention relates to a device for automated synthesis of oligo- and polysaccharides on a solid support comprising a reaction vessel, a reagent storing component, a reagent delivery system, a cooling device for cooling reaction vessel, and a pre-cooling device for pre-cooling the reagents to be supplied.

    专利号:US-6440703-B1
    优先权日:1997-12-01
    标 题 :Enzymatic synthesis of gangliosides
    发明人:DEFREES SHAWN
    权利人:NEOSE TECHNOLOGIES INC
    摘要:This invention provides methods for practical in vitro synthesis of gangliosides and other glycolipids. The synthetic methods typically involve enzymatic synthesis, or a combination of enzymatic and chemical synthesis. One or more of the enzymatic steps is preferably carried out in the presence of an organic solvent.

    专利号:US-10751419-B2
    优先权日:2014-05-01
    标题:Method for synthesis of reactive conjugate clusters
    发明人:MIGAWA MICHAEL T; YU JINGHUA; WAN W BRAD; PATEL SAYTEN P; VASQUEZ GUILLERMO; KINBERGER GARTH A; PRAKASH THAZHA P; SETH PUNIT P; SWAYZE ERIC E
    权利人:IONIS PHARMACEUTICALS INC
    摘要:Provided herein are improved methods for the synthesis of reactive conjugate clusters and intermediates used in such methods. In particular, improvements are provided that enhance the synthesis of reactive conjugate clusters by reducing the number of synthetic steps required. The reactive conjugate clusters prepared using the improved methods don't include any transacylation impurities that are formed using existing methods. The improved methods also provide an increase in overall yield and a cost benefit over existing methods.
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    合成参考文献


    摘要:Faber, K.; Glueck, S. M., Science of Synthesis: Biocatalysis in Organic Synthesis, (2015) 1, 461.
    参考文献:10.1007/s002849900033
    摘要:Van Reenen CA, Dicks LM. Evaluation of numerical analysis of random amplified polymorphic DNA (RAPD)-PCR as a method to differentiate Lactobacillus plantarum and Lactobacillus pentosus. Curr Microbiol. 1996 Apr;32(4):183–7. doi: 10.1007/s002849900033.
    参考文献:10.1007/bf00731453
    摘要:Fan JQ, Huynh LH, Reinhold BB, Reinhold VN, Takegawa K, Iwahara S, Kondo A, Kato I, Lee YC. Transfer of Man9GlcNAc to L-fucose by endo-beta-N-acetylglucosaminidase from Arthrobacter protophormiae. Glycoconj J. 1996 Aug;13(4):643–52. doi: 10.1007/bf00731453.
    参考文献:10.1007/s002849900124
    摘要:Inglis PW, Peberdy JF. News & Notes: Isolation of Ewingella americana from the Cultivated Mushroom, Agaricus bisporus. Current Microbiology. 1996 Nov 01;33(5):334–7. doi: 10.1007/s002849900124.
    参考文献:10.1007/s00253-004-1578-6
    摘要:Jrgensen F, Hansen OC, Stougaard P. Enzymatic conversion of d-galactose to d-tagatose: heterologous expression and characterisation of a thermostable l-arabinose isomerase from Thermoanaerobacter mathranii. Applied Microbiology and Biotechnology. 2004 Jun 01;64(6):816–22. doi: 10.1007/s00253-004-1578-6.
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