CAS: 492-62-6; (2S,3R,4S,5S,6R)-6-(Hydroxymethyl)Tetrahydro-2H-Pyran-2,3,4,5-Tetraol

该化合物是生物中一种单沙律和基本碳水化合物,是一种六碳糖(Hexose),其分子配方为C6H12O6. 以其 -亚甲状形形式,第一个碳原子上的氢氧基质组在循环结构中向下倾斜,这是一种阴性形态.这种组合在其再活动以及与其他生物分子的互动中发挥着关键作用. -D-甘蔗糖因其多种盐基组而高度溶于水中,可形成与水分子的氢联结.它作为细胞的主要能量源,并参与各种代谢途径,包括透析和柠檬酸循环. 此外,D-甘蔗可以聚合成对植物和动物的能量储存至关重要的聚亚类植物和甘油. D-糖的甜度和易腐蚀性在植物和动物的能量储存中,其糖性和易化性在生物化学中扮演了重要的基础性化学和化学元性作用.

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合成工艺路线路线简述

    📜Rubiyunnanin B置于β-Glucosidase体系中,用 水 作为反应溶剂,化学反应 72.0H,以1 Mg的收率获得产物a-无水葡萄糖酯
    参考文献:云南茜草的两个新的环状六肽茜草宁a和b
    标题:云南茜草的两个新的环状六肽茜草宁a和b
    摘要:两个新的环状六肽,分别称为rubiyunnanins A(1)和b(2),从滇滇茜草的根中分离出来.通过光谱分析和理论计算广泛阐明了它们的结构.提出了ras,1和2的可能的生物合成途径.在lps和ifn-γ诱导的raw 264.7鼠巨噬细胞中,化合物2对11种癌细胞系表现出中等的细胞毒性,并抑制一氧化氮(no)的产生.
    DOI:10.1016/j.Tetlet.2010.07.066

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    专利信息


    专利号:US-2012190064-A1
    优先权日:2004-10-01
    标题 :Feeding buffers, systems, and methods for in vitro synthesis of biomolecules
    发明人:KUDLICKI WIESLAW ANTONI; KEPPETIPOLA SHIRANTHI; FLETCHER JULIA; GETBEHEAD ASHLEY ELAINE; KATZEN FEDERICO; VOZZA-BROWN LAURA
    权利人:KUDLICKI WIESLAW ANTONI; KEPPETIPOLA SHIRANTHI; FLETCHER JULIA; GETBEHEAD ASHLEY ELAINE; KATZEN FEDERICO; VOZZA-BROWN LAURA; LIFE TECHNOLOGIES CORP
    摘要:Compositions, methods and kits for in vitro systems for synthesis of biomolecules such as polypeptides, are provided herein. Cell extracts that provide enhanced yields of soluble proteins using in vitro protein synthesis methods are provided. The invention also includes methods for producing high yields of proteins by the addition of a feeding solution that includes amino acids and an energy source to an ongoing in vitro synthesis system. The invention also includes methods of using a high-yield in vitro synthesis system to produce large quantities of proteins with incorporated labeled amino acids for analysis by methods such as by NMR. The invention further includes vectors for enhanced production of proteins from nucleic acid templates using in vitro synthesis systems.

    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:WO-0142264-A1
    优先权日:1999-12-10
    标 题 :Method for the synthesis of sialylated oligosaccharide donors
    发明人:MEHTA SEEMA; GILBERT MICHEL; WAKARCHUK WARREN W; WHITFIELD DENNIS M
    权利人:CA NAT RESEARCH COUNCIL; MEHTA SEEMA; GILBERT MICHEL; WAKARCHUK WARREN W; WHITFIELD DENNIS M
    摘要:A method for the synthesis of aryl thioglycosides comprising a sialylated residue of β-D-galactose is disclosed. The method consists of preparing by a chemical synthesis a non-sialylated aryl thioglycoside, and enzymatically sialylating the latter with a sialic acid in the presence of a suitable sialyltransferase. The sialylated aryl thioglycoside is then chemically derivatized by standard procedures, to provide a derivative suitable for use as a donor in chemical syntheses of sialylated oligosaccharides. The derivatized sialylated aryl thioglycosides are prepared in high yields, due to reduced number of chemical and purification steps involved in the process. Derivatized aryl thioglycosides useful as building blocks for the synthesis of biologically active sialylated oligosaccharides are also disclosed.

    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-9012625-B2
    优先权日:2009-04-07
    标 题 :Method for the synthesis of a trisaccharide
    发明人:DÉKANY GYULA; Ã?GOSTON KÃ?ROLY; BAJZA ISTVAN; BOUTET JULIEN; BØJSTRUP MARIE; FANEFJORD METTE; PÉREZ FIGUEROA IGNACIO; HEDEROS MARKUS; HORVATH FERENC; KOVÃ?CS-PÉNZES PIROSKA; KRÖGER LARS; OLSSON JOHAN; RÖHRIG CHRISTOPH; SCHROVEN ANDREAS; VRASIDAS IOANNIS
    权利人:DÉKANY GYULA; Ã?GOSTON KÃ?ROLY; BAJZA ISTVAN; BOUTET JULIEN; BØJSTRUP MARIE; FANEFJORD METTE; PÉREZ FIGUEROA IGNACIO; HEDEROS MARKUS; HORVATH FERENC; KOVÃ?CS-PÉNZES PIROSKA; KRÖGER LARS; OLSSON JOHAN; RÖHRIG CHRISTOPH; SCHROVEN ANDREAS; VRASIDAS IOANNIS; GLYCOM AS
    摘要:The present invention relates to an improved synthesis of a trisaccharide of the formula (1), novel intermediates used in the synthesis and the preparation of the intermediates.

    专利号:US-5532147-A
    优先权日:1991-08-06
    标题:Enzymatic method for synthesis of carbohydrates
    发明人:NILSSON KURT
    摘要:A synthetic method in which is included at least one process, which is characterized by that a glycosidase (EC 3.2) is used to catalyse a reaction between a partially protected galactose derivative, or a partially protected glucose derivative, and a glycosyl doner, which is an oligosaccharide or a monosaccharide glycoside, is described. The process is suitable for synthesis of carbohydrate derivatives or for synthesis of partially protected carbohydrate intermediates which are suitable for further synthesis e.g. of blood group determinants A and B, or other carbohydrates.

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    合成参考文献


    参考文献:10.1186/1471-2180-10-47
    摘要:Toledo MS, Tagliari L, Suzuki E, Silva CM, Straus AH, Takahashi HK. Effect of anti-glycosphingolipid monoclonal antibodies in pathogenic fungal growth and differentiation. Characterization of monoclonal antibody MEST-3 directed to Manpalpha1-->3Manpalpha1-->2IPC. BMC Microbiol. 2010 Feb 15;10():47.
    参考文献:10.1007/s00705-005-0669-8
    摘要:Seddas P, Boissinot S. Glycosylation of beet western yellows virus proteins is implicated in the aphid transmission of the virus. Arch Virol. 2006 May;151(5):967–84. doi: 10.1007/s00705-005-0669-8.
    参考文献:10.1107/s1600536811008257
    摘要:Hussen RSD, Heidelberg T, Rodzi NZM, Ng SW, Tiekink ERT. 4-Formylphenyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside. Acta Crystallogr E Struct Rep Online. 2011 Mar 09;67(4):o826. doi: 10.1107/s1600536811008257.
    参考文献:10.1007/s11010-011-0995-y
    摘要:Hoyer FF, Albrecht L, Nickenig G, Müller C. Selective inhibition of leukotriene receptor BLT-2 reduces vascular oxidative stress and improves endothelial function in ApoE−/− mice. Molecular and Cellular Biochemistry. 2011 Jul 14;359(1-2):25–31. doi: 10.1007/s11010-011-0995-y.
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