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2-(cholestan-3β-yl)ethanamine | 1031890-68-2

中文名称
——
中文别名
——
英文名称
2-(cholestan-3β-yl)ethanamine
英文别名
3β-aminoethyl-5α-cholestane;2-[(3S,5S,8R,9S,10S,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]ethanamine
2-(cholestan-3β-yl)ethanamine化学式
CAS
1031890-68-2
化学式
C29H53N
mdl
——
分子量
415.747
InChiKey
BNICBSRNZPZLHZ-LKHYOGBDSA-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):
    10.2
  • 重原子数:
    30
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    26
  • 氢给体数:
    1
  • 氢受体数:
    1

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

  • 作为反应物:
    描述:
    2-(cholestan-3β-yl)ethanamine盐酸 作用下, 以 乙醚 为溶剂, 生成 3β-aminoethyl-5α-cholestane hydrochloride
    参考文献:
    名称:
    WO2008/68037
    摘要:
    公开号:
  • 作为产物:
    描述:
    5-Alpha-胆甾烷-3-酮 在 lithium aluminium tetrahydride 、 palladium on activated charcoal 、 氢气 、 lithium hydroxide 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 9.0h, 生成 2-(cholestan-3β-yl)ethanamine
    参考文献:
    名称:
    Evaluation of steroidal amines as lipid raft modulators and potential anti-influenza agents
    摘要:
    The influenza A virus (IFV) possesses a highly ordered cholesterol-rich lipid envelope. A specific composition and structure of this membrane raft envelope are essential for viral entry into cells and virus budding. Several steroidal amines were investigated for antiviral activity against IFV. Both, a positively charged amino function and the highly hydrophobic (ClogP >= 5.9) ring system are required for IC50 values in the low mu M range. An amino substituent is preferential to an azacyclic A-ring. We showed that these compounds either disrupt or augment membrane rafts and in some cases inactivate the free virus. Some of the compounds also interfere with virus budding. The antiviral selectivity improved in the series 3-amino, 3-aminomethyl, 3-aminoethyl, or by introducing an OH function in the A-ring. Steroidal amines show a new mode of antiviral action in directly targeting the virus envelope and its biological functions. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2013.07.015
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文献信息

  • WO2008/68037
    申请人:——
    公开号:——
    公开(公告)日:——
  • Evaluation of steroidal amines as lipid raft modulators and potential anti-influenza agents
    作者:Sameer Agarwal、Cornelia Schroeder、Georg Schlechtingen、Tobias Braxmeier、Gary Jennings、Hans-Joachim Knölker
    DOI:10.1016/j.bmcl.2013.07.015
    日期:2013.9
    The influenza A virus (IFV) possesses a highly ordered cholesterol-rich lipid envelope. A specific composition and structure of this membrane raft envelope are essential for viral entry into cells and virus budding. Several steroidal amines were investigated for antiviral activity against IFV. Both, a positively charged amino function and the highly hydrophobic (ClogP >= 5.9) ring system are required for IC50 values in the low mu M range. An amino substituent is preferential to an azacyclic A-ring. We showed that these compounds either disrupt or augment membrane rafts and in some cases inactivate the free virus. Some of the compounds also interfere with virus budding. The antiviral selectivity improved in the series 3-amino, 3-aminomethyl, 3-aminoethyl, or by introducing an OH function in the A-ring. Steroidal amines show a new mode of antiviral action in directly targeting the virus envelope and its biological functions. (C) 2013 Elsevier Ltd. All rights reserved.
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