CAS: 4338-47-0; (2R,3R,4S,5R)-2-(6-((Furan-2-Ylmethyl)Amino)-9H-Purin-9-yl)-5-(Hydroxymethyl)Tetrahydrofuran-3,4-Diol

该化合物是细胞基因动脉的核核素派衍生物,以其在诸如扩散和老龄化等细胞过程的调节作用著称.它作为三磷酸树脂的新陈代谢的前体,参与核酸新陈代谢,并可能影响腺代谢受体信号.研究表明,由于它能够激活鼠标并增强NAD+生物合成,因此在研究与年龄有关的细胞路径和氧化应激反应方面可能应用.它的高度纯度和稳定性使它适合生物化学和细胞研究.基涅丁肋骨因其在探索实验模型中的灵敏性,DNA修复和代谢调节机制方面的有用性而特别受到重视.

结构式图片

上下游产品

CAS号4753-68-8 2-furanylmethan... | CAS号2004-06-0 6-氯嘌呤核苷 | CAS号98-01-1 糠醛 | CAS号58-61-7 腺苷 | CAS号617-89-0 糠胺 | CAS号105499-44-3 2,3,5-tri-O-ace... | CAS号1121-47-7 2-呋喃甲醛肟 | CAS号342-69-8 6-(甲硫基)-9-β-D-呋... | CAS号7387-58-8 [5-(6-acetamido... | CAS号525-79-1 6-糠氨基嘌呤 | CAS号18646-11-2 α-D-ribofuranos...

合成工艺路线路线简述

    📜6-N-2',3',5'-Tri-O-Tetraacetyladenosine置于甲醇,氨,三苯基膦,偶氮二甲酸二乙酯体系中,用 四氢呋喃 作为反应溶剂,化学反应 48.0H,反应生成 激动素核苷
    参考文献:N6-乙酰基-2',3',5'-三-O-乙酰腺苷;区域选择性n6-烷基化的便捷"缺失"底物
    标题:N6-乙酰基-2',3',5'-三-O-乙酰腺苷;区域选择性n6-烷基化的便捷"缺失"底物
    摘要:在咪唑存在下,在室温下用甲醇对五乙酰基腺苷2进行选择性的n-脱乙酰基化反应,建立了一种简单有效的n 6-乙酰基2',3',5'-Tri-O-乙酰腺苷(1)路线. .利用2和1的粗混合物,通过腺苷与乙酸酐在吡啶中在升高的温度下反应制备的混合物,详细说明了1的制备合成.从腺苷开始,总产率为1,为80-85%.结果表明1是选择性n 6的便捷底物-烷基化.该研究揭示了在1与活化的烷基卤化物的碱促进反应和1与醇的光延反应中相同的区域选择性.制备了一系列的n 6-烷基腺苷5A-F.通过使用核苷磷酸化酶和碱性磷酸酶的组合对母体核苷衍生物5B,D,E进行酶促转化来制备细胞分裂素6B,D,E. 细胞分裂素-腺苷衍生物-N 6-烷基化-区域选择性-Mitsunobu反应-核苷磷酸化酶
    DOI:10.1055/s-0030-1260090

    海关参考信息

    专利信息


    专利号:US-2024207302-A1
    优先权日:2021-04-01
    标 题 :Antiviral compounds, methods for the manufacturing of compounds, antiviral pharmaceutical composition, use of the compounds and method for the oral treatment of coronavirus infection and related diseases thereof
    发明人:CALIXTO JOãO BATISTA; RABI NALLAR JAIME ALBERTO; LOPES E SOUZA THIAGO MORENO
    权利人:CALIXTO JOAO BATISTA; RABI NALLAR JAIME ALBERTO; LOPES E SOUZA THIAGO MORENO
    摘要:The present invention relates to antiviral compounds selected from cytokinins, their nucleosides and nucleotide analogs, and their prodrugs as inhibitors of viral RNA synthesis, or their salts, solvates, derivatives, or even combinations of aforementioned compounds, for prophylactic treatment, curative (therapeutic) or mitigative coronavirus infection, represented by human and veterinary coronavirus, SARS-COV-2 and MHIV, and for the treatment of individuals potentially exposed to COVID-19. The present invention also comprises the methods for the manufacturing of such compounds, the antiviral pharmaceutical composition containing the compounds of the invention, as well as the use of the compounds, combinations of compounds, and method for the prophylactic, curative (therapeutic) or mitigative treatment of coronavirus infection, represented by coronavirus, in especial SARS-COV-2 and of patients with COVID-19, individual infected with SARS-COV-2 or potentially exposed to this virus. The antiviral activity of the compounds of this invention against SARS-COV-2 was greatly enhanced by inhibiting the 3′-5′-exonuclease. Synergistic results of the compounds according to the present invention were obtained from the combination with repurposed drugs.

    专利号:US-2023241088-A1
    优先权日:2022-01-17
    标 题 :Composition for preventing or treating lung cancer comprising ortho-topolin riboside as active ingredient
    发明人:CHOI HYUNG-KYOON; LEE HWANHUI
    权利人:CHUNG ANG UNIV INDUSTRY ACADEMY COOPERATION FOUNDATION
    摘要:The present disclosure relates to a composition for preventing or treating lung cancer, including ortho topolin riboside (oTR) as an active ingredient, wherein oTR showed the highest cytotoxicity among all tested compounds against NSCLC cells, oTR reduced synthesis of amino acid and pyrimidine as well as glycolytic function in NSCLC cells and xenograft tumors.

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    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: Kadlecová A, Jirsa T, Novák O, Kammenga J, Strnad M, Voller J. Natural plant hormones cytokinins increase stress resistance and longevity of Caenorhabditis elegans. Biogerontology. 2017 Dec 18. doi: 10.1007/s10522-017-9742-4. [Epub ahead of print] doi: 10.3892/ol.2017.5725. Epub 2017 Feb 13.
    3: Osgerby L, Lai YC, Thornton PJ, Amalfitano J, Le Duff CS, Jabeen I, Kadri H, Miccoli A, Tucker JHR, Muqit MMK, Mehellou Y. Kinetin Riboside and Its ProTides Activate the Parkinson's Disease Associated PTEN-Induced Putative Kinase 1 (PINK1) Independent of Mitochondrial Depolarization. J Med Chem. 2017 Apr 27;60(8):3518-3524. doi: 10.1021/acs.jmedchem.6b01897. Epub 2017 Mar 28.
    4: Voller J, Béres T, Zatloukal M, Kaminski PA, Niemann P, Doležal K, Džubák P, Hajdúch M, Strnad M. The natural cytokinin 2OH3MeOBAR induces cell death by a mechanism that is different from that of the "classical" cytokinin ribosides. Phytochemistry. 2017 Apr;136:156-164. doi: 10.1016/j.phytochem.2017.01.004. Epub 2017 Jan 30. doi: 10.1016/j.foodchem.2016.08.012. Epub 2016 Aug 5. doi: 10.1021/acs.analchem.6b00408. Epub 2016 Mar 24. doi: 10.1007/s00216-015-8782-3. Epub 2015 May 30. doi: 10.1016/j.plantsci.2013.09.012. Epub 2013 Oct 2. doi: 10.1093/pcp/pct156. Epub 2013 Nov 4. doi: 10.1111/j.2042-7158.2012.01526.x. Epub 2012 Apr 25. Review. doi: 10.1080/15257770.2012.681825. doi: 10.1182/blood-2011-01-330019. Epub 2011 Dec 9. doi: 10.1016/j.plaphy.2011.08.004. Epub 2011 Aug 22. doi: 10.1002/jcb.23132. Erratum in: J Cell Biochem. 2015 Jan;116(1): 202. doi: 10.1016/j.phytochem.2010.04.018. Epub 2010 Jun 1. doi: 10.1074/jbc.M109.032466. Epub 2010 Feb 5.

    合成参考文献


    参考文献:10.1016/j.phytochem.2017.01.004
    摘要:Voller J, Béres T, Zatloukal M, Kaminski PA, Niemann P, Doležal K, Džubák P, Hajdúch M, Strnad M. The natural cytokinin 2OH3MeOBAR induces cell death by a mechanism that is different from that of the "classical" cytokinin ribosides. Phytochemistry. 2017 Apr;136():156–64. doi: 10.1016/j.phytochem.2017.01.004.
    参考文献:10.1016/j.bmcl.2017.01.040
    摘要:Orlov AA, Drenichev MS, Oslovsky VE, Kurochkin NN, Solyev PN, Kozlovskaya LI, Palyulin VA, Karganova GG, Mikhailov SN, Osolodkin DI. New tools in nucleoside toolbox of tick-borne encephalitis virus reproduction inhibitors. Bioorganic & Medicinal Chemistry Letters. 2017 Mar;27(5):1267–73. doi: 10.1016/j.bmcl.2017.01.040.
    参考文献:10.1021/jm00156a016
    摘要:Kusachi S, Thompson RD, Yamada N, Daly DT, Olsson RA. Dog coronary artery adenosine receptor: structure of the N6-aryl subregion. J Med Chem. 1986 Jun;29(6):989–96. doi: 10.1021/jm00156a016.
    参考文献:10.1074/jbc.m109.032466
    摘要:Choi B, Feng L, Yoon HS. FKBP38 Protects Bcl-2 from Caspase-dependent Degradation. Journal of Biological Chemistry. 2010 Mar;285(13):9770–9. doi: 10.1074/jbc.m109.032466.
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