CAS: 66323-49-7; 3'-Nh2-Ddg

该化合物是一个经修改的核核素,在生化研究和药物应用中起着重要作用.作为瓜诺西ine的衍生物,它以3'位置为代表,缺乏氢氧基基,2'和3'位置上没有氢氧基,将它归类为二'和三'位置上.这种结构改变具有独特的特性,使它成为核酸合成和功能研究的宝贵工具.没有2'氢氧基化合物组,使它无法进一步接受磷酸化,这对于抗病毒和抗癌药物的发展至关重要,因为它能够抑制病毒复制和细胞扩散.此外,3'Amino-2',3'dideoxyguanosine可以被纳入DNA菌株,使研究人员能够调查它对核酸相互作用和稳定性的影响.它的CAS编号为6623-49-7,有助于在化学数据库中识别它,有助于探索其在分子生物学中的潜在治疗应用和运动机制.

结构式图片

相似化合物

85326-06-3 961-07-9 207121-55-9

上下游产品

3'-amino-3'-deoxythymidine G 5'-O-trityl-2,3'-anhydrothymidine 3'-azido-2',3'-deoxythymidine 3'-tritylamino-2',3'-dideoxyguanosine 2-isobutyryl-3'-NH-trityl-2',3'-dideoxyguanosineN2-isobutyryl-3'-NH-trityl-2',3'-dideoxyguanosine

合成工艺路线路线简述

    5'-三苯甲基-2'-脱氧-2,3'-双脱氢胸苷置于吡啶,Ammonium Hydroxide,Phosphate Buffer,叠氮化锂,Cells Of E.Coli Bmt-38,Na-Acetate Buffer,溶剂黄146,三苯基膦体系中,化学反应 35.0H,反应生成 3'-氨基-2',3'-双脱氧鸟苷
    参考文献:Chemical-Enzymatic Synthesis Of 3'-Amino-2',3'-Dideoxy-β-D-Ribofuranosides Of Natural Heterocyclic Bases And Their 5'-Monophosphates
    标题:Chemical-Enzymatic Synthesis Of 3'-Amino-2',3'-Dideoxy-β-D-Ribofuranosides Of Natural Heterocyclic Bases And Their 5'-Monophosphates
    摘要:Treatment Of O-2,3'-Anhydro-5'-O-Trityl Derivatives Of Thymidine (1) And 2'-Deoxyuridine (2) With Lithium Azide In Dimethylformamide At 150 Degrees C Resulted In The Formation Of The Corresponding Isomeric 3'-Azido-2',3'-Dideoxy-5'-O-Trityl-Beta-D-Ribofuranosyl N1-(The Major Products) And N-3-Nucleosides (3/4 And 5/6). 3'-Amino-2',3'-Dideoxy-Beta-D-Ribofuranosides Of Thymidine [thd(3'Nh2)],Uridine [durd(3'Nh2)],And Cytidine [dcyd(3'Nh2)] Were Synthesized From The Corresponding 3'-Azido Derivatives. The Thd(3'Nh2) And Durd(3'Nh2) Were Used As Donors Of Carbohydrate Moiety In The Reaction Of Enzymatic Transglycosylation Of Adenine And Guanine To Afford Dado(3'Nh2) And Dguo(3'Nh2). The Substrate Activity Of Dn(3'Nh2) Vs. Nucleoside Phosphotransferase Of The Whole Cells Of Erwinia Herbicola Was Studied.
    DOI:10.1080/15257779408013281

    海关参考信息

    专利信息


    专利号:US-9365606-B2
    优先权日:2004-07-02
    标题 :Synthesis of protected 3′-amino nucleoside monomers
    发明人:GRYAZNOV SERGEI M; PONGRACZ KRISZTINA; ZIELINSKA DARIA
    权利人:GERON CORP
    摘要:Orthogonally protected 3′-amino nucleoside monomers and efficient methods for their synthesis are described. The methods employ selective protection of the 3′-amino group in the presence of the unprotected nucleoside base.

    专利号:US-2007065922-A1
    优先权日:2005-09-21
    标题 :Biocatalytic synthesis of aminodeoxy purine N9-beta-D-nucleosides containing 3-amino-3-deoxy-beta-D-ribofuranose, 3-amino-2,3-dideoxy-beta-D-ribofuranose, and 2-amino-2-deoxy-beta-D-ribofuranose as sugar moieties
    发明人:BARAI VLADIMIR N; EROSHEVSKAYA LUDMILLA A; MIKHAILOPULO IGOR A; AZHAYEV ALEX V; LAPINJOKI SEPPO P
    权利人:METKINEN OY
    摘要:Purine N 9 -β-D-nucleosides containing 3-amino-3-deoxy-β-D-ribofaranose, 3-amino-2,3-dideoxy-β-D-ribofuranose, and 2-amino-2-deoxy-β-D-ribofuranose as sugar moieties are synthesized by biocatalytic transglycosylation of purine bases and the respective 3′-amino-3′-deoxyuridine, 3′-amino-3′-deoxythymidine and 2′-amino-2′-deoxyuridine as donors of the carbohydrate moiety, and the cells of Escherichia coli as a biocatalyst or glutaraldehyde (GA) treated cells of Escherichia coli as a biocatalyst or a mixture of thymidine (uridine) phosphorylase and purine nucleoside phosphorylase.

    专利号:US-2024300992-A1
    优先权日:2004-07-02
    标题:Synthesis of Protected 3'-amino Nucleoside Monomers

    专利号:US-10738073-B2
    优先权日:2004-07-02
    标 题 :Synthesis of protected 3′-amino nucleoside monomers

    专利号:US-2009105468-A1
    优先权日:2004-07-02
    标 题 :Synthesis of Protected 3'-Amino Nucleoside Monomers

    专利号:US-2023089101-A1
    优先权日:2004-07-02
    标题:Synthesis of Protected 3'-amino Nucleoside Monomers
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    合成参考文献


    参考文献:10.1089/aid.1988.4.457
    摘要:Hartmann H, Vogt MW, Durno AG, Hirsch MS, Hunsmann G, Eckstein F. Enhanced in vitro inhibition of HIV-1 replication by 3'-fluoro-3'-deoxythymidine compared to several other nucleoside analogs. AIDS Res Hum Retroviruses. 1988 Dec;4(6):457–66. doi: 10.1089/aid.1988.4.457.
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