CAS: 2620-62-4; (2R,3R,4S,5R)-2-(6-(Dimethylamino)-9H-Purin-9-yl)-5-(Hydroxymethyl)Tetrahydrofuran-3,4-Diol

该化合物是源自腺素的经修改的核素,其特点是在腺基第6位的氮原子中存在两个附属于氮原子的甲基组,这种修改在各种生物过程,特别是在RNA新陈代谢和条例中起着重要作用.N6-二甲基甲胺已知会影响基因的表达,并参与管理氨氨的稳定性和翻译.它通常存在于eukarydellies细胞中,是包括tRNA和RRNA在内的某些RNA物种的关键组成部分.这种修改的存在会影响RNA的结构和功能,影响细胞过程,例如插管和翻译效率.此外,N6-二甲基乙胺已经研究过它可能对各种疾病,包括癌症的潜在影响,在这些疾病中,经过改变的甲基化模式会影响基因表达特征.其化学结构和特性使它成为生物化学化学和分子生物学研究的一个主题.

结构式图片

上下游产品

(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(dimethylamino)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate dimethyl amine (2R,3R,4R,5R)-2-((benzoyloxy)methyl)-5-(6-chloro-9H-purin-9-yl)tetrahydrofuran-3,4-diyl dibenzoate N6,N6,S-trimethyl-2-thio-isoguanosineN6,N6,S-trimethyl-2-thio-isoguanosineO2',O3'-((R)-benzylidene)-N6,N6-dimethyl-adenosineO2',O3'-((R)-benzylidene)-N6,N6-dimethyl-adenosine 6,N6'-dimethyladenosine2',3'-O-isopropylidene-N6,N6'-dimethyladenosine 6,N6-Dimethyl-5'-O-trityladenosineN6,N6-Dimethyl-5'-O-trityladenosine 2',3',5'-tri-O-benzyl-N,N-dimethyladenosine

合成工艺路线路线简述

    2',3',5'-三乙酰腺苷置于吡啶体系中,用 水 用作溶剂,化学反应 20.67H,反应生成N6,N6-二甲基腺苷
    参考文献:Miles,Robert W.; Samano,Vicente; Robins,Morris J.,Journal Of The American Chemical Society,1995,Vol. 117,# 22,P. 5951-5957
    标题:Miles,Robert W.; Samano,Vicente; Robins,Morris J.,Journal Of The American Chemical Society,1995,Vol. 117,# 22,P. 5951-5957

    海关参考信息

    专利信息


    专利号:US-12146136-B2
    优先权日:2020-03-26
    标题:Synthesis of modified oligonucleotides with increased stability
    发明人:KHVOROVA ANASTASIA; ROUX LOÃ?C MAURICE RENÉ JEAN; YAMADA KEN
    权利人:UNIV MASSACHUSETTS
    摘要:This disclosure relates to the synthesis of novel modified oligonucleotides. The synthesis of novel phosphoramidites are also provided.

    专利号:US-2023212204-A1
    优先权日:2020-01-16
    标题:Reagents and their use for modular enantiodivergent synthesis of c-p bonds
    发明人:XU DONGMIN; RIVAS-BASCÓN NAZARET; KNOUSE KYLE W; PADIAL NATALIA; ZHENG BIN; VANTOUROUT JULIEN; SCHMIDT MICHAEL; EASTGATE MARTIN D; BARAN PHI
    权利人:BRISTOL MYERS SQUIBB CO; SCRIPPS RESEARCH INST
    摘要:The disclosure describes chiral P(V)-based reagents and their uses for the modular, scalable, and stereospecific synthesis of chiral phosphines, phosphine oxides and particular oligonucleotides.

    专利号:WO-2025217610-A1
    优先权日:2024-04-12
    标题:Systems and methods for enzymatic oligonucleotide synthesis
    发明人:ENTWISTLE DAVID; GAUNTLETT DEREK; MILLER MICHAEL; REEVES RYAN; WATTS DAVID
    权利人:CODEXIS INC
    摘要:The present invention provides for methods and systems for template-free synthesis of an oligonucleotide, and methods of using the systems as disclosed herein for template-free synthesis of an oligonucleotide.

    专利号:US-2014378538-A1
    优先权日:2011-12-14
    标 题:Methods of responding to a biothreat
    发明人:BANCEL STEPHANE
    权利人:MODERMA THERAPEUTICS INC
    摘要:The present disclosure provides for devices, in particular mobile devices, which may be used in the synthesis of modified nucleic acid molecules, in particular modified mRNA molecules. The device for making the modified nucleosides, modified nucleotides and modified nucleic acids (e.g., mRNA) disclosed herein may be mobile devices comprising at least one sample block for insertion of one or more sample vessels, a device base with electronic control units for the sample block, a voltage supply, and one or more reagent(s) for the synthesis of at least one nucleic acid.

    专利号:US-9790531-B2
    优先权日:2012-08-14
    标 题 :Enzymes and polymerases for the synthesis of RNA
    发明人:WANG YUXUN; RAMAKRISHNAN DIVAKAR; DE FOUGEROLLES ANTONIN; WHORISKEY SUSAN
    权利人:MODERNATX INC
    摘要:The invention relates to compositions and methods for the design, evolution, preparation, and/or manufacture of enzymes for use with polynucleotides, primary transcripts and mmRNA molecules.

    专利号:US-2025207163-A1
    优先权日:2022-03-25
    标 题:Methods and apparatus for synthesizing nucleic acids
    发明人:HOPKINS PATRYCJA A; SHAHSAVARI SHAHIEN; BEGOYAN VAGARSHAK; NJUMA OLIVE J; DEBENHAM HOLLY S; EFCAVITCH J WILLIAM; ALBIZATI KIM F
    权利人:MOLECULAR ASSEMBLIES INC
    摘要:Methods for the synthesis of polynucleotides using polymerases nucleotide analogs with labile terminator groups that allow stepwise addition of nucleotides are described. These nucleotide analogs may have a modification on 3′, 2′, or 3′-2′-bridged hydroxyl groups or on nucleobase moieties and can be used in the synthesis of natural or modified polynucleotides suitable for use in biological systems. The labile terminator groups are removed under mild conditions or by enzymes. They are accepted as substrates by polymerases. The synthesis may be carried out on a surface.
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    合成参考文献


    摘要:D. M. G. Martin and C. B. Reese, J. Chem. Soc. (C) 1968, 1731.
    参考文献:10.1021/jm00149a016
    摘要:Kusachi S, Thompson RD, Bugni WJ, Yamada N, Olsson RA. Dog coronary artery adenosine receptor: structure of the N6-alkyl subregion. J Med Chem. 1985 Nov;28(11):1636–43. doi: 10.1021/jm00149a016.
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