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9-<5-O-(monomethoxytrityl)-3-deoxy-3-thio-3-S,2-O-diacetyl-β-D-ribofuranosyl>hypoxanthine | 174466-93-4

中文名称
——
中文别名
——
英文名称
9-<5-O-(monomethoxytrityl)-3-deoxy-3-thio-3-S,2-O-diacetyl-β-D-ribofuranosyl>hypoxanthine
英文别名
[(2R,3S,4R,5R)-4-acetylsulfanyl-5-[[(4-methoxyphenyl)-diphenylmethoxy]methyl]-2-(6-oxo-3H-purin-9-yl)oxolan-3-yl] acetate
9-<5-O-(monomethoxytrityl)-3-deoxy-3-thio-3-S,2-O-diacetyl-β-D-ribofuranosyl>hypoxanthine化学式
CAS
174466-93-4
化学式
C34H32N4O7S
mdl
——
分子量
640.717
InChiKey
PGNQIIQTPCDGBO-JHZZHVAFSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.61
  • 重原子数:
    46.0
  • 可旋转键数:
    10.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    134.63
  • 氢给体数:
    1.0
  • 氢受体数:
    11.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    9-<5-O-(monomethoxytrityl)-3-deoxy-3-thio-3-S,2-O-diacetyl-β-D-ribofuranosyl>hypoxanthine吡啶sodium hydroxide溶剂黄146 作用下, 以 二氯甲烷 为溶剂, 反应 8.5h, 生成 Thiophosphoric acid O-[(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3,4-dihydroxy-tetrahydro-furan-2-ylmethyl] ester S-[(2R,3S,4S,5R)-4-hydroxy-2-hydroxymethyl-5-(6-oxo-1,6-dihydro-purin-9-yl)-tetrahydro-furan-3-yl] ester; compound with triethyl-amine
    参考文献:
    名称:
    Synthesis and Characterization of an RNA Dinucleotide Containing a 3‘-S-Phosphorothiolate Linkage
    摘要:
    The synthesis of an RNA dinucleotide (IspU) containing a 3'-S-phosphorothiolate linkage is described. The compound is prepared from 9-(3-deoxy-3-iodo-beta-D-xylofuranosyl)hyperanthine with installation of the phosphorothiolate group via an Arbusov reaction and protection of the ribose 2'-hydroxyl as a silyl ether. IspU is found to be a substrate for several enzymes including T4 polynucleotide kinase, snake venom phosphodiesterase, and ribonuclease T-2. Base-catalyzed cleavage of the dinucleotide is accelerated (similar to 2000-fold) relative to that of the phosphate-linked compound IpU. Product characterization and kinetic analysis show that IspU is cleaved through the same mechanism as IpU. The observed rate acceleration is argued to reflect stabilization of the anionic transition state by the polarizable sulfur atom.
    DOI:
    10.1021/ja9616903
  • 作为产物:
    参考文献:
    名称:
    Synthesis and Characterization of an RNA Dinucleotide Containing a 3‘-S-Phosphorothiolate Linkage
    摘要:
    The synthesis of an RNA dinucleotide (IspU) containing a 3'-S-phosphorothiolate linkage is described. The compound is prepared from 9-(3-deoxy-3-iodo-beta-D-xylofuranosyl)hyperanthine with installation of the phosphorothiolate group via an Arbusov reaction and protection of the ribose 2'-hydroxyl as a silyl ether. IspU is found to be a substrate for several enzymes including T4 polynucleotide kinase, snake venom phosphodiesterase, and ribonuclease T-2. Base-catalyzed cleavage of the dinucleotide is accelerated (similar to 2000-fold) relative to that of the phosphate-linked compound IpU. Product characterization and kinetic analysis show that IspU is cleaved through the same mechanism as IpU. The observed rate acceleration is argued to reflect stabilization of the anionic transition state by the polarizable sulfur atom.
    DOI:
    10.1021/ja9616903
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文献信息

  • Synthesis and structure of S-nucleosidyl S-aryl disulfides and their reaction with phosphites
    作者:Adrian P. Higson、Gerard K. Scott、David J. Earnshaw、Anthony D. Baxter、Roger A. Taylor、Richard Cosstick
    DOI:10.1016/0040-4020(95)00936-1
    日期:1996.1
    corresponding thioesters is described. This procedure has been used for the preparation of a ribonucleoside disulphide (8d), a key intermediate for the synthesis of oligoribonucleotides containing 3′-S-phosphorothiolate linkages. The regioselectivity of the Arbusov reaction of 8d with phosphites has been examined. The X-ray structure of 3′-deoxy-3′-S-(2-nitrophenyldisulfanyl)thymidine (9b) is also reported
    描述了由相应的酯制备S-核苷基S-芳基二硫化物的一般方法。该方法已经用于制备核糖核苷二硫化物(8d),核糖核苷二硫化物(8d)是合成含有3'- S-硫代磷酸酯键的寡核糖核苷酸的关键中间体。研究了8d与亚磷酸酯的Arbusov反应的区域选择性。还报道了3′-脱氧-3′- S-(2-硝基苯基二烷基)胸苷的X射线结构(9b)。
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同类化合物

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