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mannitol-1,6-bis-phosphate | 13400-43-6

中文名称
——
中文别名
——
英文名称
mannitol-1,6-bis-phosphate
英文别名
mannitol bis-phosphate;O1,O6-diphosphono-D-mannitol;O1,O6-Diphosphono-D-mannit;1,6-Bis-phosphonooxy-D-manno-hexan-2,3,4,5-tetraol;D-Mannitol-1,6-diphosphate;[(2R,3R,4R,5R)-2,3,4,5-tetrahydroxy-6-phosphonooxyhexyl] dihydrogen phosphate
mannitol-1,6-bis-phosphate化学式
CAS
13400-43-6
化学式
C6H16O12P2
mdl
——
分子量
342.133
InChiKey
WOYYTQHMNDWRCW-KVTDHHQDSA-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

物化性质

  • 沸点:
    801.4±75.0 °C(Predicted)
  • 密度:
    2.010±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -5.8
  • 重原子数:
    20
  • 可旋转键数:
    9
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    214
  • 氢给体数:
    8
  • 氢受体数:
    12

反应信息

  • 作为产物:
    描述:
    (2R,3R,4R,5R)-2,3,4,5-tetrakis(benzyloxy)hexane-1,6-diyl bis(dihydrogen phosphate) 在 palladium on activated charcoal 氢气 作用下, 20.0 ℃ 、100.0 kPa 条件下, 生成 mannitol-1,6-bis-phosphate
    参考文献:
    名称:
    Separate synthesis and evaluation of glucitol bis-phosphate and mannitol bis-phosphate, as competitive inhibitors of fructose bis-phosphate aldolases
    摘要:
    We report the first unambiguous syntheses of glucitol-1,6-bis-phosphate and mannitol-1,6-bis-phosphate and their competitive inhibition of various fructose bis-phosphate aldolases. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.01.076
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文献信息

  • Ukita; Nagasawa, Chemical and pharmaceutical bulletin, 1959, vol. 7, p. 401,406
    作者:Ukita、Nagasawa
    DOI:——
    日期:——
  • [EN] ACTIVATION OF RAS BY A FRUCTOSE-1,6-BISPHOSPHATE / GUANINE NUCLEOTIDE EXCHANGE PROTEIN COMPLEX<br/>[FR] ACTIVATION DE RAS PAR UN COMPLEXE DE PROTÉINE D'ÉCHANGE NUCLÉOTIDIQUE FRUCTOSE-1,6-BISPHOSPHATE / GUANINE
    申请人:VIB VZW
    公开号:WO2015011222A1
    公开(公告)日:2015-01-29
    The present invention relates to an isolated fructose-1,6-bisphosphate / SOS complex. The invention relates further to the use of the complex to screen for compounds that modulate the activation of Ras, and the use of yeast strains for said screening. The invention relates also to compounds, disrupting the fructose-1,6-bisphosphate / SOS complex and the use of such compounds in the treatment of cancer.
  • Separate synthesis and evaluation of glucitol bis-phosphate and mannitol bis-phosphate, as competitive inhibitors of fructose bis-phosphate aldolases
    作者:Charles-Gabin Mabiala-Bassiloua、Magdalena Zwolinska、Helene Therisod、Jurgen Sygusch、Michel Therisod
    DOI:10.1016/j.bmcl.2008.01.076
    日期:2008.3
    We report the first unambiguous syntheses of glucitol-1,6-bis-phosphate and mannitol-1,6-bis-phosphate and their competitive inhibition of various fructose bis-phosphate aldolases. (C) 2008 Elsevier Ltd. All rights reserved.
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