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3α-(tert-butyldimethylsilyloxy)-20-oxo-5β-pregnan-7α-yl nicotinate | 1177358-16-5

中文名称
——
中文别名
——
英文名称
3α-(tert-butyldimethylsilyloxy)-20-oxo-5β-pregnan-7α-yl nicotinate
英文别名
[(3R,5R,7R,8R,9S,10S,13S,14S,17S)-17-acetyl-3-[tert-butyl(dimethyl)silyl]oxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-7-yl] pyridine-3-carboxylate
3α-(tert-butyldimethylsilyloxy)-20-oxo-5β-pregnan-7α-yl nicotinate化学式
CAS
1177358-16-5
化学式
C33H51NO4Si
mdl
——
分子量
553.858
InChiKey
YORUKZWVLGAWAX-BLJJSTCZSA-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):
    7.86
  • 重原子数:
    39
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.79
  • 拓扑面积:
    65.5
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

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文献信息

  • Synthesis of C3, C5, and C7 pregnane derivatives and their effect on NMDA receptor responses in cultured rat hippocampal neurons
    作者:Eva Stastna、Hana Chodounska、Vladimir Pouzar、Vojtech Kapras、Jirina Borovska、Ondrej Cais、Ladislav Vyklicky
    DOI:10.1016/j.steroids.2008.11.011
    日期:2009.2
    The synthesis of several novel 5 alpha- and 5 beta-20-oxo-pegnane derivatives substituted in the position 3 and 7 of the steroid skeleton is described. Activity of synthesized compounds was studied in voltage-clamped cultured rat hippocampal neurons. Substituted derivatives inhibited NMDA-elicited neuronal activity. The relationship between biological activity and structure is discussed. (C) 2008 Published by Elsevier Inc.
  • ANIONIC PREGNANE COMPOUNDS, METHOD FOR THEIR PRODUCING AND USE OF THEM
    申请人:Ústav organické chemie a biochemie Akademie ved Ceské republiky, v.v.i.
    公开号:EP2313424B1
    公开(公告)日:2014-04-23
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