CAS: 374750-30-8; 2'-C-Methylguanosine

该化合物是一种经修改的核核素,在各种生物过程,特别是在RNA新陈代谢过程中具有重要作用,其特点是,在2'的糖位置上存在一个甲基组,将其与其他标准糖区别开来,这种改变可能影响RNA分子的稳定性和功能,影响其在细胞过程中的相互作用和作用.化合物经常出现在tRNA中,并参与基因表达和蛋白合成的调节.其结构特征包括一个与肋糖相连的纯基(guanine),而甲基组则加强了分子的水分恐惧性,并有可能影响其与其他生物颗粒素的结合性. 2'C-乙基瓜纳在医药化学和生物技术领域也具有兴趣,因为它可能作为治疗剂或研究RNA动态的工具.

结构式图片

相似化合物

118-00-3 38819-10-2 26578-09-6

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CAS号890131-90-5 N-乙酰基-2’-C-甲基鸟苷... | CAS号19962-37-9 N-2-乙酰鸟嘌呤 | CAS号10310-21-1 2-氨基-6-氯嘌呤 | CAS号1188418-39-4 3-(β-D-2-C-meth... | CAS号1188418-36-1 3-(β-D-2-C-meth...

合成工艺路线路线简述

    N-2-乙酰鸟嘌呤置于三氟甲磺酸三甲基硅酯,氨体系中,用 甲醇,甲苯 用作溶剂,化学反应 72.0H,反应生成2-C-甲基鸟苷
    参考文献:有效合成2'-C-β-甲基鸟苷
    标题:有效合成2'-C-β-甲基鸟苷
    摘要:2'-β-甲基核苷具有潜在的治疗剂和核苷类似物的潜在价值,可用于探索rna生物学.在这里,我们开发了有效合成2'-C-β-甲基鸟苷(3)的策略.从开始-1,2,3,5-四ø-苯甲酰基-2-ç-β甲基d-Ribofuranose(1)和ñ 2-乙酰基鸟嘌呤中,我们在两个步骤中制得标题化合物(78%总收率)具有高立体选择性(β/α> 99:1)和高区域选择性(n9 / N7> 99:1).将该策略扩展至鸟嘌呤的经典合成方法还导致高立体选择性(β/α= 99:1)和改善的区域选择性(n9 / N7 = 97:3).
    Doi:10.1021/jo0602165

    海关参考信息

    专利信息


    专利号:US-11858953-B2
    优先权日:2018-04-04
    标 题:Compositions and methods for synthesis of phosphorylated molecules
    发明人:CHAPUT JOHN; LIAO JEN-YU; BALA SAIKAT
    权利人:UNIV CALIFORNIA
    摘要:The invention provides compositions and methods for synthesis of phosphorylated organic compounds, including nucleoside triphosphates.

    专利号:US-2022356182-A1
    优先权日:2009-03-27
    标题 :Inhibitors of hepatitis c virus replication
    发明人:COBURN CRAIG A; LUDMERER STEVEN W; LIU KUN; WU HAO; SOLL RICHARD; ZHONG BIN; ZHU JIAN
    权利人:MERCK SHARP & DOHME
    摘要:The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5A inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5A activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.

    专利号:WO-2011106929-A1
    优先权日:2010-03-02
    标题:Inhibitors of hepatitis c virus ns5b polymerase
    发明人:MCCOMAS CASEY CAMERON; LIVERTON NIGEL J; HABERMANN JOERG; KOCH UWE; NARJES FRANK; LI PENG; PENG XUANJIA; SOLL RICHARD; WU HAO
    权利人:MERCK SHARP & DOHME; ANGELETTI P IST RICHERCHE BIO; MCCOMAS CASEY CAMERON; LIVERTON NIGEL J; HABERMANN JOERG; KOCH UWE; NARJES FRANK; LI PENG; PENG XUANJIA; SOLL RICHARD; WU HAO
    摘要:Compounds of formula I that are used as hepatitis C virus (HCV) NS5B polymerase inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5B polymerase activity, for treating or preventing HCV infection and for inhibiting HCV viral replication and /or viral production in a cell-based system.

    专利号:US-9493461-B2
    优先权日:2013-02-07
    标 题 :Tetracyclic heterocycle compounds and methods of use thereof for the treatment of hepatitis C
    发明人:DAI XING; LIU HONG; PALANI ANANDAN; HE SHUWEN; LAI ZHONG; NARGUND RAVI; MARCANTONIO KAREN; XIAO DONG; BROCKUNIER LINDA L; ZORN NICOLAS; DANG QUN; PENG XUANJIA; LI PENG
    权利人:MERCK SHARP & DOHME
    摘要:The present invention relates to compounds of formula I that are useful as hepatitis C virus (HCV) NS5B polymerase inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5B polymerase activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.

    专利号:WO-2011106986-A1
    优先权日:2010-03-02
    标题:Inhibitors of hepatitis c virus ns5b polymerase
    发明人:MCCOMAS CASEY CAMERON; LIVERTON NIGEL J; SOLL RICHARD; LI PENG; PENG XUANJIA; WU HAO
    权利人:MERCK SHARP & DOHME; MCCOMAS CASEY CAMERON; LIVERTON NIGEL J; SOLL RICHARD; LI PENG; PENG XUANJIA; WU HAO
    摘要:Compounds of formula (I) that are used as hepatitis C virus (HCV) NS5B polymerase inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5B polymerase activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and /or viral production in a cell-based system. Wherein Z, R 30 , R 40 , R 50 and R 60 of compounds of formula (I) are herein defined as in the description.

    专利号:US-9242998-B2
    优先权日:2013-02-07
    标题 :Tetracyclic heterocycle compounds and methods of use thereof for the treatment of hepatitis C
    发明人:HE SHUWEN; DAI XING; PALANI ANANDAN; NARGUND RAVI; LAI ZHONG; ZORN NICOLAS; XIAO DONG; DANG QUN; MCCOMAS CASEY C; LI PENG; PENG XUANJIA; SOLL RICHARD
    权利人:HE SHUWEN; DAI XING; PALANI ANANDAN; NARGUND RAVI; LAI ZHONG; ZORN NICOLAS; XIAO DONG; DANG QUN; MCCOMAS CASEY C; LI PENG; PENG XUANJIA; SOLL RICHARD; MERCK SHARP & DOHME
    摘要:The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5B polymerase inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5B polymerase activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.
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    主要参考文献

    参考标题: Compositions And Methods For Synthesis Of Phosphorylated Molecules Compositions Et Procédés De Synthèse De Molécules Phosphorylées
    摘要:The Invention Provides Compositions And Methods For Synthesis Of Phosphorylated Organic Compounds, Including Nucleoside Triphosphates.

    合成参考文献


    参考文献:10.1016/j.ejmech.2015.10.002
    摘要:Briguglio I, Loddo R, Laurini E, Fermeglia M, Piras S, Corona P, Giunchedi P, Gavini E, Sanna G, Giliberti G, Ibba C, Farci P, La Colla P, Pricl S, Carta A. Synthesis, cytotoxicity and antiviral evaluation of new series of imidazo[4,5-g]quinoline and pyrido[2,3-g]quinoxalinone derivatives. European Journal of Medicinal Chemistry. 2015 Nov;105():63–79. doi: 10.1016/j.ejmech.2015.10.002.
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