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α-D-glucosyl pyrophosphate | 92642-57-4

中文名称
——
中文别名
——
英文名称
α-D-glucosyl pyrophosphate
英文别名
Diphosphoric acid 1-alpha-d-glucopyranosyl ester;phosphono [(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] hydrogen phosphate
α-D-glucosyl pyrophosphate化学式
CAS
92642-57-4
化学式
C6H14O12P2
mdl
——
分子量
340.117
InChiKey
GHRQAEPJQRJDHX-VFUOTHLCSA-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):
    -4.8
  • 重原子数:
    20
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    203
  • 氢给体数:
    7
  • 氢受体数:
    12

反应信息

  • 作为产物:
    参考文献:
    名称:
    TSUHAKO, MITSUTOMO;SUEYOSHI, CHIYOKO;BABA, YOSHINOBU;MIYAJIMA, TOHORU;OHA+, CHEM. LETT.,(1987) N 7, 1431-1434
    摘要:
    DOI:
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文献信息

  • Synthesis of polyprenyl pyrophosphate sugars from unprotected mono- and oligo-saccharide phosphates
    作者:Leonid L. Danilov、Sergei D. Maltsev、Vladimir N. Shibaev、Nikolai K. Kochetkov
    DOI:10.1016/s0008-6215(00)85534-2
    日期:1981.2
  • TSUHAKO, MITSUTOMO;SUEYOSHI, CHIYOKO;BABA, YOSHINOBU;MIYAJIMA, TOHORU;OHA+, CHEM. LETT.,(1987) N 7, 1431-1434
    作者:TSUHAKO, MITSUTOMO、SUEYOSHI, CHIYOKO、BABA, YOSHINOBU、MIYAJIMA, TOHORU、OHA+
    DOI:——
    日期:——
  • [EN] GLYCORANDOMIZATION AND THE PRODUCTION OF NOVEL ERYTHRONOLIDE AND COUMARIN ANALOGS<br/>[FR] GLYCORANDOMISATION ET PRODUCTION DE NOUVEAUX ANALOGUES D'ERYTHRONOLIDE ET DE COUMARINE
    申请人:SLOAN KETTERING INST CANCER
    公开号:WO2002079150A2
    公开(公告)日:2002-10-10
    The present invention provides combinatorial methods for rapidly generating a diverse library of glycorandomized structures, comprising incubating one or more aglycons and a pool of NDP-sugars in the presence of a glycosyltransferase. The glycosyltransferase may be one that is associated with or involved in production of natural secondary metabolites, or one which is putatively associated with or involved in production of natural secondary metabolites. The glycosyltransferase may show significant flexibility with respect to its NDP-sugar donors and/or its aglycons. NDP-sugar donors may be commercially available, or may be produced by utilizing mutant or wild type nucleotidyltransferases significant flexibility with respect to their substrates.
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