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6-Hydroxy-Duloxetine Glucuronide | 741693-84-5

中文名称
——
中文别名
——
英文名称
6-Hydroxy-Duloxetine Glucuronide
英文别名
XE7RH9J8MC;(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-[(1S)-3-(methylamino)-1-thiophen-2-ylpropoxy]naphthalen-2-yl]oxyoxane-2-carboxylic acid
6-Hydroxy-Duloxetine Glucuronide化学式
CAS
741693-84-5
化学式
C24H27NO8S
mdl
——
分子量
489.546
InChiKey
GRIXJAFEBWYBJE-ANUWOGMRSA-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:
    776.6±60.0 °C(Predicted)
  • 密度:
    1.450±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.1
  • 重原子数:
    34
  • 可旋转键数:
    9
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    166
  • 氢给体数:
    5
  • 氢受体数:
    10

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

反应信息

  • 作为产物:
    描述:
    5-氨基-2-萘酚 在 lithium hydroxide 、 tetrafluoroboric acid 、 4-甲基苯磺酸吡啶 、 sodium hydride 、 溶剂黄146 、 sodium nitrite 作用下, 以 甲醇N,N-二甲基甲酰胺 为溶剂, 生成 6-Hydroxy-Duloxetine Glucuronide
    参考文献:
    名称:
    Synthesis and biological activity of some known and putative duloxetine metabolites
    摘要:
    Several putative phase I duloxetine metabolites, 4-hydroxy-, 5-hydroxy-, 6-hydroxy-, 5-hydroxy-6-methoxy-, 6-hydroxy5-methoxy-, 5,6-dihydroxy-, and 4,6-dihydroxyduloxetine were synthesized, and their phase II metabolite as glucuronide or sulfate conjugates were also synthesized. Their in vitro binding activities were compared to that of parent compound duloxetine. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2004.04.066
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文献信息

  • Synthesis and biological activity of some known and putative duloxetine metabolites
    作者:F. Kuo、T.A. Gillespie、P. Kulanthaivel、R.J. Lantz、T.W. Ma、D.L. Nelson、P.G. Threlkeld、W.J. Wheeler、P. Yi、M. Zmijewski
    DOI:10.1016/j.bmcl.2004.04.066
    日期:2004.7
    Several putative phase I duloxetine metabolites, 4-hydroxy-, 5-hydroxy-, 6-hydroxy-, 5-hydroxy-6-methoxy-, 6-hydroxy5-methoxy-, 5,6-dihydroxy-, and 4,6-dihydroxyduloxetine were synthesized, and their phase II metabolite as glucuronide or sulfate conjugates were also synthesized. Their in vitro binding activities were compared to that of parent compound duloxetine. (C) 2004 Elsevier Ltd. All rights reserved.
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