CAS: 14000-31-8; Pyrophosphate

该化合物是一种无机化合物,其独特结构由两个磷酸盐组组成,由一种氢化物结合物组成,该化合物通常以配方P2O74为代表,表明其阴离子性.磷酸盐通常被作为盐或酯,在各种生物化学过程中,特别是在能源转移和储存方面,它起着关键作用,因为它参与了ATP(乙酸三磷酸)的合成和水解,就溶液而言,热磷盐一般在水中溶解,使其在各种应用中有用,包括生物化学和分子生物学.此外,热磷酸盐可以作为一种铬化剂,结合金属离子和影响酶反应.其稳定性取决于环境条件,例如pH和温度,而且在某些条件下,它可以水解成丙磷酸盐.总的来说,热磷酸盐在生物系统和工业应用中都是一种重要的化合物.

结构式图片

欧盟法规

C&L通报

合成工艺路线路线简述

    📜连二磷酸置于cl2体系中,用 水 用作溶剂,以>99的收率获得二磷酸酯
    参考文献:Blaser,B.,Chemische Berichte,1953,Vol. 86,P. 563-572
    标题:Blaser,B.,Chemische Berichte,1953,Vol. 86,P. 563-572

    专利信息


    专利号:US-9376461-B2
    优先权日:2011-06-06
    标 题:Non-enzymatic synthesis of O-acetyl-ADP-ribose and analogues thereof
    发明人:KOPPETSCH KARSTEN; SZCZEPANKIEWICZ BRUCE G; PERNI ROBERT B
    权利人:KOPPETSCH KARSTEN; SZCZEPANKIEWICZ BRUCE G; PERNI ROBERT B; GLAXOSMITHKLINE LLC
    摘要:Provided herein is a simple, one-step, non-enzymatic synthesis of O-Acetyl-ADP-ribose (OAADPR) from NAD and sodium acetate in acetic acid. The extension of this reaction to other carboxylic acids, demonstrates that the reaction between NAD, and NAD analogs produces mixtures of the corresponding 2′- and 3′-carboxylic esters. Included are O-carboxyl-ADP-ribose compounds and corresponding methods of synthesis (e.g., O-propionyl-ADP-ribose, O-succinyl-ADP-ribose, O-malonyl-ADP-ribose), as well as non-adenosine nucleoside compounds.

    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-9720061-A1
    优先权日:1995-11-30
    标题:Synthesis of hyaluronic acid
    发明人:WONG CHI-HUEY; DELUCA CLAUDIO
    权利人:SCRIPPS RESEARCH INST; WONG CHI HUEY; DELUCA CLAUDIO
    摘要:A preparative enzymatic synthesis of hyaluronic acid (HA) from UDP-N-acetyl-D-glucosamine (UDP-GlcNAc) and UDP-glucuronic acid (UDP-GlcA) catalyzed by hyaluronic acid synthase is coupled with regeneration of the sugar nucleotides. Polymerizing UDP-GlcA and UDP-GlcNAc to form hyaluronic acid results in the formation of released UDP. The released UDP is, in turn, employed in the regeneration of UDP-GlcA and UDP-GlcNAc. Use of the released UDP for regenerating UDP-GlcA and UDP-GlcNAc prevents a build-up of these compounds and prevents or reduces feed back inhibition of the hyaluronic acid synthase reaction that would otherwise be caused by such build-up. Accordingly, the product yield is enhanced by the recycling of these compounds.

    专利号:WO-9323416-A1
    优先权日:1992-05-13
    标 题:Chemical synthesis of 2',3'-dideoxynucleoside 5'-triphosphates
    发明人:MATULIC-ADAMIC JASENKA; BEIGELMAN LEONID
    权利人:US BIOCHEMICAL CORP
    摘要:Method for synthesis of 2',3'-dideoxynucleoside 5'-triphosphates by contacting a 2',3'-dideoxynucleoside with a phosphorylating agent in the presence of a proton removing reagent.

    专利号:US-6875866-B2
    优先权日:2002-02-21
    标题:Process for synthesis of D1 receptor antagonists
    发明人:DAHANUKAR VILAS H; ECKERT JEFFREY M; GALA DINESH; LUCAS BRIAN; SCHUMACHER DORIS P; ZAVIALOV ILIA
    权利人:SCHERING CORP
    摘要:In one embodiment, the present invention describes the synthesis of a compound of formula n n nand intermediates therefor.

    专利号:US-2015376219-A1
    优先权日:2014-06-30
    标题 :Selective Preparations of Purine Nucleosides and Nucleotides: Reagents and Methods
    发明人:ZHONG MINGHONG
    权利人:ZHONG MINGHONG
    摘要:A process of regiospecific synthesis of N-9 purine nucleoside analogs in either solution or solid phase synthesis is described. The introduction of the sugar moiety or its analogue on to a 6-heteroarylium purine or its mesomeric betaine so that formation of only the N-9 position regioisomers of the purine nucleoside analogs (either D or L enantiomers) is obtained. This regiospecific introduction of the sugar moiety allows the synthesis of purine nucleoside analogs in high yields without formation of the N-7-positional regioisomers, while the 6-heteroaryliums are leaving groups facilitated for nucleophilic displacement. Solid supported 6-heterarylium purine bases can be used for purine based library synthesis and synthesis of nucleotide monophosphates and polyphosphates. Processes for providing novel 6-heteroarylium purines and their corresponding mesomeric betaines for the regiospecific synthesis of N-9 purine nucleoside analogs and nucleotides are described.

    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

    合成参考文献


    摘要:Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases., 29(12)(53), 1985
    参考文献:10.1021/jm991008q
    摘要:Flohr A, Aemissegger A, Hilvert D. alpha-Functionalized phosphonylphosphinates: synthesis and evaluation as transcarbamoylase inhibitors. J Med Chem. 1999 Jul 15;42(14):2633–40. doi: 10.1021/jm991008q.
    参考文献:10.1038/s42003-019-0458-7
    摘要:LinWu S, Tu Y, Tsai T, Maestre-Reyna M, Liu M, Wu W, Huang J, Chi H, Chang W, Chiou C, Wang AH-, Lee J, Tsai M. Thermococcus sp. 9°N DNA polymerase exhibits 3′-esterase activity that can be harnessed for DNA sequencing. Communications Biology. 2019 Jun 20;2(1):224. doi: 10.1038/s42003-019-0458-7.
    参考文献:10.1016/j.xplc.2020.100051
    摘要:Chen Q, Li J, Liu Z, Mitsuhashi T, Zhang Y, Liu H, Ma Y, He J, Shinada T, Sato T, Wang Y, Liu H, Abe I, Zhang P, Wang G. Molecular Basis for Sesterterpene Diversity Produced by Plant Terpene Synthases. Plant Communications. 2020 Sep;1(5):100051. doi: 10.1016/j.xplc.2020.100051.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知