CAS: 7403-25-0; 3'-Nh2-Dda

该化合物是一种经修改的核核素类比,其特点是肋骨环的2和3位置上没有氢氧基,代之以氨基组,在3'的位置上,这种结构改变增强了其抗酶降解的稳定性,使其对生化和药理研究很有价值.该化合物是核素类比与潜在的抗病毒或抗癌活动合成的先兆.其独特的配置允许有选择地纳入核酸序列,促进关于DNA/RNA相互作用和酶机制的研究.研究人员利用它来研究聚合酶的忠性,并设计有定制特性的改良的核糖核素.

结构式图片

相似化合物

4097-22-7 2504-55-4 958-09-8

上下游产品

9-(3-azido-2,3-dideoxy-β-D-erythro-pentofuranosyl)adenine adenine 3'-amino-3'-deoxythymidine 5'-O-trityl-2,3'-anhydrothymidine 3'-tritylamino-2',3'-dideoxyadenosine FontWeight=Bold FontSize=10 ',3'-dideoxy-3'-[(triphenylmethyl)amino]adenosineN-benzoyl-2 FontWeight=Bold FontSize=10 ',3'-dideoxy-3'-[(triphenylmethyl)amino]adenosine 3'-N-[N-allyloxycarbonyl-S-(tert-butylthio)-L-cysteinyl]-5'-O-(tert-butyldimethylsilyl)-N6,N6-{2-[3-oxo-3-(pentafluorophenyloxy)propyl]}glutaryl-9-(3'-amino-2',3'-dideoxy-β-D-ribofuranosyl)adenine

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,Glutaraldehyde-Treated Cells Of E.Coli Bm-11,Na-Acetate Buffer,溶剂黄146,三苯基膦体系中,化学反应 31.0H,反应生成 3'-氨基-2',3'-双脱氧腺苷
    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
    上海兆维科技发展有限公司
    ⚠️ 未注册 · 未认证企业
    ⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
    数据来源于公开网络搜索,平台未作核实,请自行辨别。
    🏢敬请 企业认领
    🏬开设公司展台
    📢获取免费会员权益
    🎖️点亮专属注册企业标签
    📇展现公司完整信息 样本查看立即注册认领 →
    网址: http://www.hongene.com/
    电话: 021-64757213👤
    📞上海兆维科技发展有限公司 ⚠️参考联系方式

    销售电话:021-64757213
    邮箱:info@hongene.com
    🆔 联系时候可告知是从"百琢研"平台获取的信息.
    ⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

    ⚠️ 未注册 · 未认证企业
    注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别 ✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
    第 1 / 1 页
    现货

    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


    参考文献:10.1007/978-3-642-65806-8_37
    摘要:Frederiksen S, Klenow H. 3’-Deoxyadenosine and Other Polynucleotide Chain Terminators. 1975. In: Antineoplastic and Immunosuppressive Agents. : Springer Berlin Heidelberg; 1975.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知