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MRS 1957

中文名称
——
中文别名
——
英文名称
MRS 1957
英文别名
(1S,2R,3R,6R)-1-((S)-Hydroxymethyl)-4-(6-hydroxy-purin-9-yl)-bicyclo[3.1.0]hexane-2,3-diol;9-[(1S,2R,3S,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)-2-bicyclo[3.1.0]hexanyl]-1H-purin-6-one
MRS 1957化学式
CAS
——
化学式
C12H14N4O4
mdl
——
分子量
278.268
InChiKey
ZESHFLAIHFABCS-PHPBVZTRSA-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):
    -1.7
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.58
  • 拓扑面积:
    120
  • 氢给体数:
    4
  • 氢受体数:
    6

反应信息

  • 作为产物:
    参考文献:
    名称:
    Synthesis and purine receptor affinity of 6-oxopurine nucleosides and nucleotides containing (N)-methanocarba-pseudoribose rings
    摘要:
    6-Oxopurine derivatives containing a northern (N) methanocarba modification (i.e., fused cyclopropane and cyclopentane rings in place of the ribose) were synthesized and the adenosine receptor affinity measured. Guanine or hypoxanthine was coupled at the 7-position, or 1,3-diblitylxanthine was coupled at the 9-position. The pseudoribose ring was also substituted at the 5 ' -position with an N-methyluronamide or with phosphate groups. Published by Elsevier Science Ltd.
    DOI:
    10.1016/s0960-894x(01)00450-4
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文献信息

  • Total Syntheses of a Conformationally Locked<i>North</i>-Type Methanocarba Puromycin Analogue and a Dinucleotide Derivative
    作者:Benoît Y. Michel、Peter Strazewski
    DOI:10.1002/chem.200802629
    日期:2009.6.15
    Locked in translation: Crucial insight into the ribosomal catalysis of peptide‐bond formation is expected to be gained from the target compounds, which feature conformational locking in a North‐type pucker, designed to interfere with the translation of the genetic code. The compounds were prepared from D‐ribose in 18 and 19 steps by a multi‐step synthetic route described here (see scheme).
    锁定翻译:可以从目标化合物中获得对肽键形成的核糖体催化作用的重要见解,这些化合物具有构象锁定在North- type pucker中的功能,旨在干扰遗传密码的翻译。这些化合物是由D-核糖按照此处所述的多步合成路线分18步和19步制备的(请参见方案)。
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