CAS: 14365-44-7; (2R,3R,4S,5R)-2-(6-Amino-9H-Purin-9-yl)-5-(Aminomethyl)Tetrahydrofuran-3,4-Diol

该化合物是纯核素的核素,由根基构成,在5号位置上附着在牛卵糖上,有氨基氨基;该化合物的特点是它在各种生化过程中的作用,特别是在细胞代谢和信号路径中的作用;它是腺素的衍生物,是能量转移和细胞信号传输中的关键分子;氨基质组的存在可以影响其与酶和受体的相互作用,有可能影响其生物活动.5'Aminoadenosine由于其氢氧基和氨基组,在水和表层中溶解,并呈现极性特征,使其与其他极性分子相互作用良好;其结构特征允许它参与核糖和核酸的合成,有助于蛋白合成和能量代谢等细胞功能;

结构式图片

相似化合物

58-61-7 5536-17-4 3080-29-3

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合成工艺路线路线简述

    📜N6-Benzoyl-2',3'-O-Isopropylidene-5'-O-Methylsulfonyladenosine置于lindlar'S Catalyst Sodium Azide,氢气,Sodium Methylate,三氟乙酸体系中,用 甲醇,N,N-二甲基甲酰胺 用作溶剂,化学反应 28.25H,反应生成5-氨基腺苷酸
    参考文献:Design,Synthesis,And Molecular Modeling Studies Of 5'-Deoxy-5'-Ureidoadenosine: 5'-Ureido Group As Multiple Hydrogen Bonding Donor In The Active Site Of S-Adenosylhomocysteine Hydrolase
    标题:Design,Synthesis,And Molecular Modeling Studies Of 5'-Deoxy-5'-Ureidoadenosine: 5'-Ureido Group As Multiple Hydrogen Bonding Donor In The Active Site Of S-Adenosylhomocysteine Hydrolase
    摘要:5'-Deoxy-5'-Ureidoadenosine Was Designed And Synthesized As A Potent Inhibitor Of S-Adenosylhomocysteine Hydrolase (Sah),In Which 5'-Ureido Group Acted As Multiple Hydrogen Bonding Donor In Binding With Active Site Residues Of Sah In The Molecular Modeling Study. (C) 2007 Published By Elsevier Ltd.
    Doi:10.1016/j.Bmcl.2007.06.013

    海关参考信息

    专利信息


    专利号:US-2003134303-A1
    优先权日:2001-12-11
    标 题:Adenine nucleotide-binding protein-directed probes, and methods of their synthesis and use
    发明人:CAMPBELL DAVID A; WASH PAUL
    权利人:ACTIVX BIOSCIENCES INC
    摘要:The invention relates to compositions and methods for the synthesis and use of Adenosine nucleotide binding protein-directed affinity labels. Adenosine nucleotide binding proteins may be labeled with probes comprising adenosine, or an analogue thereof, functionalized at the 5′ position with reactive group capable of reacting with an amino acid side chain functionality at an adenosine nucleotide binding site, and at the 2′ or 3′ position with a TAG for sequestering and/or identifying the resulting conjugate. The probes may be used for determining the presence or amount of one or more adenosine nucleotide binding proteins in a complex mixture, particularly a cellular mixture, for screening for drugs, and other purposes associated with the presence of the adenine nucleotide-binding protein(s) in a cell or changes in the presence, amount, activity, or relative concentration of the active adenosine nucleotide-binding protein.

    专利号:US-7999087-B2
    优先权日:2006-11-15
    标 题:2′-silyl containing thiocarbonate protecting groups for RNA synthesis
    发明人:DELLINGER DOUGLAS J; SIERZCHALA AGNIESZKA; CARUTHERS MARVIN H; DELLINGER GERALDINE F
    权利人:AGILENT TECHNOLOGIES INC
    摘要:Nucleoside monomers, nucleic acids, e.g., oligonucleotides and polynucleotides, methods of making each, methods of deprotecting each, and the like are disclosed herein. Aspects of the invention include 2′ silyl containing thiocarbonate protecting groups. Corresponding compositions and methods are provided.

    专利号:US-9067961-B2
    优先权日:2007-05-10
    标 题 :Thiocarbon-protecting groups for RNA synthesis
    发明人:DELLINGER DOUGLAS J; SIERZCHALA AGNIESZKA B; TURNER JOHN; MYERSON JOEL; KUPIHAR ZOLTAN; FERREIRA FERNANDO; CARUTHERS MARVIN H; DELLINGER GERALDINE F
    权利人:DELLINGER DOUGLAS J; SIERZCHALA AGNIESZKA B; TURNER JOHN; MYERSON JOEL; KUPIHAR ZOLTAN; FERREIRA FERNANDO; CARUTHERS MARVIN H; DELLINGER GERALDINE F; AGILENT TECHNOLOGIES INC; UNIV COLORADO DENVER
    摘要:Aspects of the invention include 2′ protected nucleoside monomers that are protected at the 2′ site with thiocarbon protecting groups. Thiocarbon protecting groups of interest include thiocarbonate, thionocarbonate, dithiocarbonate groups, as well as thionocarbamate protecting groups. Aspects of the invention further include nucleic acids that include the protecting groups of the invention, as well as methods of synthesizing nucleic acids using the protecting groups of the invention.

    专利号:EP-1578931-A4
    优先权日:2002-07-16
    标 题:METHODS FOR IDENTIFYING COMPOUNDS THAT MODULATE THE SYNTHESIS OF IL-4 RECEPTOR-MEDIATED IGE USING ADENOSINE KINASE

    专利号:WO-2004007680-A2
    优先权日:2002-07-16
    标题:Methods of identifying compounds that modulate il-4 receptor-mediated ige synthesis utilizing an adenosine kinase

    专利号:WO-03050248-A2
    优先权日:2001-12-11
    标 题:Adenine nucleotide-binding protein-directed probes and methods of their synthesis and use

    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

    主要参考文献


    1: Stier I, Kiss A. Cytosine-to-uracil deamination by SssI DNA methyltransferase. PLoS One. 2013 Oct 21;8(10):e79003. doi: 10.1371/journal.pone.0079003. eCollection 2013.
    2: Wiesner JB, Ugarkar BG, Castellino AJ, Barankiewicz J, Dumas DP, Gruber HE, Foster AC, Erion MD. Adenosine kinase inhibitors as a novel approach to anticonvulsant therapy. J Pharmacol Exp Ther. 1999 Jun;289(3):1669-77.

    合成参考文献


    参考文献:10.1080/14756366.2022.2070909
    摘要:Kaur S, Nieto NS, McDonald P, Beck JR, Honzatko RB, Roy A, Nelson SW. Discovery of small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase. Journal of Enzyme Inhibition and Medicinal Chemistry. 2022 May 05;37(1):1320–6. doi: 10.1080/14756366.2022.2070909.
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