CAS: 134-58-7; 5-Amino-1,4-Dihydro-7H-[1,2,3]Triazolo[4,5-D]Pyrimidin-7-One

该化合物是一种清净类比,在生化和药理研究中具有显著应用.它的结构上与guanine相似,使得它能够作为抗甲代谢物发挥作用,抑制纯生物合成并干扰核酸新陈代谢.这个化合物在酶抑制,微生物遗传学和癌症研究研究中特别有用,因为它能够破坏RNA和DNA合成. 8-Azaguanine 也被用作微生物培养媒介中的一种选择性剂,分离特定的变异菌菌株.它的特性和一贯性能使得它成为调查受控实验环境中代谢途径和细胞过程的可靠工具.

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CAS号2644-70-4 盐酸肼 | CAS号7803-57-8 水合肼 | CAS号1468-26-4 8-氮杂黄嘌呤 | CAS号4342-07-8 5-氨基-1H-1,2,3-噻... | CAS号4546-73-0 3-amino-9-[4-hy...

合成工艺路线路线简述

    📜6-羟基-2,4,5-三氨基嘧啶置于硫酸,Sodium Nitrite体系中,化学反应生成8-氮鸟嘌呤
    参考文献:嘌呤,嘧啶和三唑并嘧啶的紫外吸收光谱.
    标题:嘌呤,嘧啶和三唑并嘧啶的紫外吸收光谱.
    摘要:
    Doi:10.1021/ja01191A102

    专利信息


    专利号:US-2004242897-A1
    优先权日:2002-07-31
    标题 :Universal support media for synthesis of oligomeric compounds
    发明人:GUZAEV ANDREI P; MANOHARAN MUTHIAH
    摘要:Compounds for the synthesis of oligomeric compounds, particularly oligonucleotides and oligonucleotide mimetics, are provided. In addition, methods for functionalizing a support medium with a first monomeric subunit and methods for the synthesis of oligomeric compounds utilizing the novel compounds bound to support media are provided.

    专利号:US-2024092821-A1
    优先权日:2020-03-31
    标题:Synthesis of oligonucleotides and related compounds
    发明人:ZHONG MINGHONG; JIN YI; GALA DINESH; PRHAVC MARIJA
    权利人:JANSSEN BIOPHARMA INC
    摘要:Methods of synthesizing oligonucleotides via new intermediates on a cleavable support having an azidomethyl moiety are disclosed. The method comprises multiple reaction cycles, each of which comprises sequential coupling a nucleoside or oligonucleotide subunit on a cleavable support having an azidomethyl moiety and a nucleoside phosphoramidite or an oligonucleotide phosphoramidite, capping, oxidation/thiolation and deblocking; followed by orthogonal cleavage of the azidomethyl support while keeping all other protecting groups intact. The method can be used in combination with a support moiety for either solid phase or liquid phase oligo synthesis. The soluble support facilitates homogeneous reactions and efficient separations by simple precipitation. The methods also provide novel intermediates useful in the synthesis of oligonucleotide conjugates.

    专利号:US-10751419-B2
    优先权日:2014-05-01
    标题:Method for synthesis of reactive conjugate clusters
    发明人:MIGAWA MICHAEL T; YU JINGHUA; WAN W BRAD; PATEL SAYTEN P; VASQUEZ GUILLERMO; KINBERGER GARTH A; PRAKASH THAZHA P; SETH PUNIT P; SWAYZE ERIC E
    权利人:IONIS PHARMACEUTICALS INC
    摘要:Provided herein are improved methods for the synthesis of reactive conjugate clusters and intermediates used in such methods. In particular, improvements are provided that enhance the synthesis of reactive conjugate clusters by reducing the number of synthetic steps required. The reactive conjugate clusters prepared using the improved methods don't include any transacylation impurities that are formed using existing methods. The improved methods also provide an increase in overall yield and a cost benefit over existing methods.

    专利号:WO-2004011474-A1
    优先权日:2002-07-31
    标题:Universal support media for synthesis of oligomeric compounds
    发明人:GUZAEV ANDREI P; MANOHARAN MUTHIAH; RAVIKUMAR VASULINGA T; KUMAR RAJU K
    权利人:ISIS PHARMACEUTICALS INC; GUZAEV ANDREI P; MANOHARAN MUTHIAH; RAVIKUMAR VASULINGA T; KUMAR RAJU K
    摘要:Compounds for the synthesis of oligomeric compounds, particularly oligonucleotide and oligonucleotide mimetics, are provided. In addition, methods for functionalizing a support medium with a first monomeric subunit and methods for the synthesis of oligomeric compounds utilizing the novel compounds bound to support media are provided.

    专利号:US-6653468-B1
    优先权日:2002-07-31
    标 题 :Universal support media for synthesis of oligomeric compounds
    发明人:GUZAEV ANDREI P; MANOHARAN MUTHIAH
    权利人:ISIS PHARMACEUTICALS INC
    摘要:Compounds for the synthesis of oligomeric compounds, particularly oligonucleotides and oligonucleotide mimetics, are provided. In addition, methods for functionalizing a support medium with a first monomeric subunit and methods for the synthesis of oligomeric compounds utilizing the novel compounds bound to support media are provided.

    专利号:WO-2023039068-A1
    优先权日:2021-09-08
    标题:Compositions and methods for synthesis of peptide nucleic acid intermediates
    发明人:COULL JAMES M; GILDEA BRIAN D
    权利人:NEUBASE THERAPEUTICS INC
    摘要:The present disclosure provides intermediates for the synthesis of peptide nucleic acid (PNA) backbones and monomers, such as cyclic intermediates, and methods of making the same.

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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: Shek R, Hilaire T, Sim J, French JB. Structural Determinants for Substrate Selectivity in Guanine Deaminase Enzymes of the Amidohydrolase Superfamily. Biochemistry. 2019 Jul 30;58(30):3280-3292. doi: 10.1021/acs.biochem.9b00341. Epub 2019 Jul 19.
    2: Chawla M, Minenkov Y, Vu KB, Oliva R, Cavallo L. Structural and Energetic Impact of Non-natural 7-Deaza-8-azaguanine, 7-Deaza-8-azaisoguanine, and Their 7-Substituted Derivatives on Hydrogen-Bond Pairing with Cytosine and Isocytosine. Chembiochem. 2019 Sep 2;20(17):2262-2270. doi: 10.1002/cbic.201900245. Epub 2019 Jul 19. doi: 10.1021/acs.jpca.9b01397. Epub 2019 Apr 1. doi: 10.1038/s41598-019-39591-7.
    5: Kim N, Choi JW, Song AY, Choi WS, Park HR, Park S, Kim I, Kim HS. Direct potentiation of NK cell cytotoxicity by 8-azaguanine with potential antineoplastic activity. Int Immunopharmacol. 2019 Feb;67:152-159. doi: 10.1016/j.intimp.2018.12.020. Epub 2018 Dec 12. doi: 10.1021/acs.bioconjchem.8b00261. Epub 2018 Jun 13. pii: e02236-17. doi: 10.1128/AAC.02236-17. Print 2018 Apr.

    合成参考文献


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    摘要:HANSCH,C ET AL. (1995)
    摘要:A. Albert. J. Chem. Soc., B 1966, 427.
    参考文献:10.1128/jvi.3.6.578-585.1969
    摘要:Pritikin WB, Reiter H. Abortive Infection of Bacillus subtilis Bacteriophage PBS1 in the Presence of Actinomycin D. J Virol. 1969 Jun;3(6):578–85. doi: 10.1128/jvi.3.6.578-585.1969.
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