CAS: 13239-97-9; 4-Amino-1-((2R,3R,4S,5R)-3,4-Dihydroxy-5-(Hydroxymethyl)Tetrahydrofuran-2-yl)Pyrimidine-2(1H)-Thione

该化合物是一种经过修改的核素类比,其二位基体环的氧原子被一个硫磺原子所取代.这种结构改变增强了其化学稳定性,并改变了其基质粘合特性,使其在核酸研究和治疗应用中具有价值.Thioket组增加了抗酶降解的抗药性,提高了其在核糖核酸合成和抗抗感反应技术中的用途.此外,2位基体碘展示了独特的光物理特性,促进了其在基于荧光的研究中的使用.它与标准的磷米化学相容性可以直接融入DNA或RNA线条,从而能够精确地修改核酸结构,功能和相互作用.

结构式图片

相似化合物

20235-78-3 13239-96-8 32738-09-3

上下游产品

α-2-Thioribocytidine
4-Methylsulfanyl-1-(β-D-Ribofuranosyl)Pyrimidine-2(1H)-Thione 25030-30-2
1-(2,3,5-Tri-O-Benzoyl-β-D-Ribofuranosyl)-4-Methylsulfanyl-1,2-Dihydropyrimidin-2-Thione 627812-08-2

合成工艺路线路线简述

    📜4-Methylsulfanyl-1-(β-D-Ribofuranosyl)Pyrimidine-2(1H)-Thione置于氨体系中,用 甲醇 用作溶剂,化学反应 24.0H,以56%的收率获得2-硫代胞苷
    参考文献:直接的嘧啶环构建:合成核碱基和核苷类似物的多功能工具
    标题:直接的嘧啶环构建:合成核碱基和核苷类似物的多功能工具
    摘要:1,2,4-三取代嘧啶的一般路线描述为从共同的关键前体二氮二烯碘化物 2 开始的一到三个步骤. 氮杂丁二烯结构单元 2 和各种异(硫代)之间的有效初步 [4+2] 环缩合反应)氰酸盐构成嘧啶骨架的原始结构.随后对杂环的结构修改允许精心制作包括核苷类似物的 1-取代嘧啶文库.(© Wiley-Vch Verlag Gmbh & Co. Kgaa,69451 Weinheim,Germany,2006)
    Doi:10.1002/ejoc.200500556

    海关参考信息

    专利信息


    专利号:US-2005130201-A1
    优先权日:2003-10-14
    标 题 :Splint-assisted enzymatic synthesis of polyribounucleotides
    发明人:DERAS MICHAEL; PLEISS JEFFREY A; SCARINGE STEPHEN
    权利人:DHARMACON INC
    摘要:The present invention comprises methods and compositions for splint-assisted enzymatic synthesis of polyribonucleotides using an RNA polymerizing enzyme. The invention provides ligating ribonucleotides comprising ligating a donor RNA molecule to an acceptor RNA molecule in the presence of RNA ligase and a splint, wherein the donor RNA molecule is comprised of at least one nucleotide and a ligation linker moiety, the acceptor RNA molecule is comprised of at least one nucleotide and a ligation linker moiety and the splint is comprised of a polyribonucleotide. The invention also provides splints for use in splint-assisted enzymatic synthesis using an RNA polymerizing enzyme.

    专利号:US-8314209-B2
    优先权日:2007-12-12
    标 题 :Lipid-assisted synthesis of polymer compounds and methods for their use
    发明人:RAJAMANI SUDHA; OLASAGASTI FELIX; DEAMER DAVID W; BENNER SEICO
    权利人:RAJAMANI SUDHA; OLASAGASTI FELIX; DEAMER DAVID W; BENNER SEICO; UNIV CALIFORNIA
    摘要:The invention herein disclosed provides for methods for the synthesis of polymers from monomers. In particular the method provides for the synthesis of polynucleotides from mononucleotides in the absence of catalytic enzymes. The method comprises providing an aqueous solution having a plurality of phospholipid molecules and monomer molecules; subjecting the aqueous solution to fluctuating temperature conditions; subjecting the aqueous solution to fluctuating cycles of drying and hydrating conditions; subjecting the aqueous solution to fluctuating [H + ] conditions; the fluctuating conditions thereby allowing formation of a chemical bond between at least two monomers to create a polymer. The invention is of particular use in the fields of molecular biology, structural biology, cell biology, molecular switches, molecular circuits, and molecular computational devices, and the manufacture thereof.

    专利号:US-2003049619-A1
    优先权日:2001-03-21
    标题 :Methods for the synthesis of polynucleotides and combinatorial libraries of polynucleotides
    发明人:DELAGRAVE SIMON; MARRS BARRY
    摘要:Methods for the synthesis of polynucleotides and derivatives thereof are provided. Methods for the preparation of combinatorial libraries of polynucleotides are also provided. In addition, methods for the preparation and identification of polynucleotides having a predetermined property are provided.

    专利号:US-11407993-B2
    优先权日:2017-02-14
    标 题 :Method for the synthesis of DNA conjugates by micellar catalysis
    发明人:BHAT AVINASH SHASHIDHAR; KLIKA SKOPIC MATEJA; BRUNSCHWEIGER ANDREAS; WEBERSKIRCH RALF
    权利人:UNIV DORTMUND TECH
    摘要:A method for the synthesis of a chimeric conjugate molecule by micellar catalysis that may form part of DNA-encoded compound libraries. A DNA-coupled organic starter molecule may be reacted with another organic compound, using a catalyst located within a micelle, to form a conjugate of an organic candidate compound coupled to a DNA identifier tag.

    专利号:US-7777023-B2
    优先权日:1998-10-23
    标题 :Method for the chemical synthesis of oligonucleotides
    发明人:VARGEESE CHANDRA; SHAFFER CHRISTOPHER; WANG WEIMIN
    权利人:SIRNA THERAPEUTICS INC
    摘要:The present invention features novel compositions, linkers, derivatized solid supports, and methods for the efficient solid phase synthesis of oligonucleotides, including RNA, DNA, RNA-DNA chimeras, and analogs thereof.

    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.

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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

    [参考文献]: Robak T, Robak P. Purine Nucleoside Analogs In The Treatment Of Rarer Chronic Lymphoid Leukemias. Curr Pharm Des. 2012;18(23):3373-88.

    合成参考文献


    参考文献:10.1007/128_2011_200
    摘要:Miller BL. DCC in the development of nucleic acid targeted and nucleic acid inspired structures. Top Curr Chem. 2012;322():107–37. doi: 10.1007/128_2011_200.
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