CAS: 488-69-7; Fosfructose

该化合物是甘蓝路径中的一个关键中间体,在细胞代谢中起着重要作用;是一种磷酸盐糖,特别是由纤维素衍生的乙氧素;化合物具有与第一和第六碳原子相连的两个磷酸盐组,这是其能源生产功能必不可少的;磷酸盐是一种无色,可溶性化合物,其结构允许其参与各种酶反应,特别是由藻类和纤维素1,6-双磷酸酯催化的酶反应;它是一个对甲状腺调节器,影响代谢途径中关键酶的活动,从而在调节基因素产生和凝解方面发挥作用;磷酸盐组的存在有助于其高能量特性,使它成为细胞内能量转移过程中的重要分子;此外,磷酸酯还参与对代谢通量的调节,是生物中能源生产与消费之间平衡的一个关键因素.

结构式图片

相似化合物

81028-91-3 56-73-5 17187-72-3

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CAS号57-50-1 蔗糖 | CAS号50-99-7 D(+)-无水葡萄糖 | CAS号717817-28-2 fructose-1,6-(b... | CAS号57-48-7 果糖 | CAS号57-04-5 二羟丙酮磷酸盐 半镁盐 水合物 | CAS号591-57-1 甘油醛3-磷酸 | CAS号127-17-3 丙酮酸 | CAS号56-81-5 甘油 | CAS号3658-77-3 2,5-二甲基-4-羟基-3(... | CAS号61-19-8 腺苷酸 | CAS号56-65-5 5'-三磷酸腺苷 | CAS号79-33-4 L-(+)-乳酸 | CAS号57-48-7 果糖 | CAS号7664-38-2 磷酸 | CAS号34168-77-9 6-氟-6-脱氧-d-吡喃葡萄糖 | CAS号10326-41-7 D-乳酸

合成工艺路线路线简述

    葡萄糖 反应生成 果糖二磷酸钠
    参考文献:Young,Biochemische Zeitschrift,1911,Vol. 32,P. 179
    标题:Young,Biochemische Zeitschrift,1911,Vol. 32,P. 179

    海关参考信息

    专利信息


    专利号:US-7229797-B1
    优先权日:1999-08-20
    标 题:Enzymatic synthesis of deoxyribonucleosides
    发明人:TISCHER WILHELM; IHLENFELDT HANS-GEORG; BARZU OCTAVIAN; SAKAMOTO HIROSHI; PISTOTNIK ELISABETH; MARLIERE PHILIPPE; POCHET SYLVIE
    权利人:PASTEUR INSTITUT
    摘要:The present invention relates to a method for the in vitro enzymatic synthesis of deoxyribonucleosides and enzymes suitable for this method.

    专利号:WO-9516049-A1
    优先权日:1993-12-08
    标题 :Catalytic chemo-enzymatic asymmetric synthesis of carbohydrates
    发明人:WONG CHI-HUEY; SHARPLESS BARRY K
    权利人:SCRIPPS RESEARCH INST; WONG CHI HUEY; SHARPLESS BARRY K
    摘要:A stereoselective synthesis of carbohydrates employs two key stereoselective steps, viz. an osmium-catalyzed asymmetric dihydroxylation (AD) of an alkene to form an aldol intermediate and an aldolase-catalyzed aldol addition reaction wherein the aldol intermediate is elongated by the addition of a ketone. Moreover, ketoses having four new stereocenters can be synthesized without the use of chiral starting materials. The stereoselectivity of the asymmetric dihydroxylation (AD) reaction is determined by the cis or trans (Z or E) stereoisomeric configuration of the alkene and by the choice of AD-mix, i.e., an AD-mix-α or AD-mix-β. The stereoselectivity of the aldolase-catalyzed addition reaction is determined by the choice of aldolase and by the stereochemistry of the aldol intermediate. Four aldolases with broad substrate specificity are sufficient to produce all possible enantiomeric combinations of the two hydroxymethylene stereocenters formed during the aldol addition reaction. Accordingly, a synthetic scheme combining an osmium-catalyzed asymmetric dihydroxylation (AD) reaction and an aldolase-catalyzed aldol addition reaction enables direct access to a wide range of carbohydrate derivatives containing up to four new hydroxymethylene stereocenters.

    专利号:US-5302520-A
    优先权日:1990-09-25
    标 题:Enzymatic synthesis of isotopically labeled carbohydrates
    发明人:GOUX WARREN J
    权利人:UNIV TEXAS
    摘要:The present invention relates to a general method of enzymatic synthesis of isotopically labeled carbohydrates, sugars and nucleosides. Labeled citric acid cycle intermediates, amino acids and ribose mononucleotides may be rapidly and conveniently synthesized from labeled pyruvate, lactate or L-alanine. The method employs a novel nicotinamide dinucleotide regeneration system which permits use of low NADH levels. The method may be manipulated to allow labeling at a variety of carbon/hydrogen sites.

    专利号:US-5576426-A
    优先权日:1988-08-30
    标 题:Aldolase catalyzed stereoselective synthesis of arabinohexulose, xyloheptulose, threohexulose and xylohexulose
    发明人:WONG CHI-HUEY; DURRWACHTER JOHN R; PEDERSON RICHARD L
    权利人:SEARLE & CO
    摘要:The present invention relates to aldolase catalyzed stereo-selective synthesis of sugars and compositions of matter comprising arabinohexulose, xyloheptulose, threohexulose, and xylohexulose.

    专利号:US-2017349928-A1
    优先权日:2014-12-31
    标 题:Methods for activating natural energy metabolism for improving yeast cell-free protein synthesis
    发明人:JEWETT MICHAEL CHRISTOPHER; ANDERSON MARK J; STARK JESSICA CAROL; HODGMAN CHARLES ERIC
    权利人:UNIV NORTHWESTERN
    摘要:Disclosed are compositions, methods, and kits for enhanced synthesis of a biological macromolecule in vitro using cell-free protein synthesis. The compositions, methods, and kits include or utilize: a cell-free extract; a phosphate-free energy source; and a phosphate source, and typically do not include an exogenous nucleoside triphosphate or an exogenous nucleoside diphosphate.

    专利号:US-10675366-B2
    优先权日:2016-08-12
    标 题 :Imaging tumor glycolysis by non-invasive measurement of pyruvate kinase M2
    发明人:BEINAT CORRINE GAYE; ALAM ISRAT SHAMIMA; JAMES MICHELLE L; GAMBHIR SANJIV S; SRINIVASAN ANANTH
    权利人:UNIV LELAND STANFORD JUNIOR
    摘要:The present disclosure provides a positron emission tomography (PET)-detectable 1-((2-fluoro-6-[18F]fluorophenyl)sulfonyl)-4-((4-methoxyphenyl)sulfonyl)piperazine ([18F]DASA-23) probe that can selectively bind to the pyruvate kinase variant M2 (PKM2) found in cancer cells, such as of human glioma. Given the importance of PKM2 in the regulation of tumor metabolism, there is an on-going need to non-invasively measure its expression through the development of PKM2-specific radiopharmaceuticals. Precursors useful for the synthesis of the radiolabeled [18F]DASA-23-PKM2-specific probe and related compounds, and their methods of synthesis, are provided. Since the half-life of the 18F isotope is approximately 110 min, it is advantageous for a practitioner to attach the radionuclide to the precursor shortly before administration. Therefore, a precursor compound suitable for receiving the radionuclide and capable of specifically binding to the PKM2 variant can be provided.
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    参考文献:10.1007/s00216-011-5207-9
    摘要:Kool J, Jonker N, Irth H, Niessen WMA. Studying protein–protein affinity and immobilized ligand–protein affinity interactions using MS-based methods. Analytical and Bioanalytical Chemistry. 2011 Jul 14;401(4):1109. doi: 10.1007/s00216-011-5207-9.
    参考文献:10.1007/s11010-011-0993-0
    摘要:Zou S, Gu Z, Ni P, Liu X, Wang J, Fan Q. SP1 plays a pivotal role for basal activity of TIGAR promoter in liver cancer cell lines. Molecular and Cellular Biochemistry. 2011 Jul 15;359(1-2):17–23. doi: 10.1007/s11010-011-0993-0.
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