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methyl (3α-aminomethyl)-3β,7α,12α-trihydroxy-5β-cholan-24-oate | 1191418-25-3

中文名称
——
中文别名
——
英文名称
methyl (3α-aminomethyl)-3β,7α,12α-trihydroxy-5β-cholan-24-oate
英文别名
methyl (4R)-4-[(3S,5R,7R,8R,9S,10S,12S,13R,14S,17R)-3-(aminomethyl)-3,7,12-trihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]pentanoate
methyl (3α-aminomethyl)-3β,7α,12α-trihydroxy-5β-cholan-24-oate化学式
CAS
1191418-25-3
化学式
C26H45NO5
mdl
——
分子量
451.647
InChiKey
ZPXFYPFXAYKHIG-SRJCIEHLSA-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):
    2.8
  • 重原子数:
    32
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.96
  • 拓扑面积:
    113
  • 氢给体数:
    4
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    methyl (3α-azidomethyl)-3β,7α,12α-trihydroxy-5β-cholan-24-oate 在 5% Pd(II)/C(eggshell) 、 氢气 作用下, 以 甲醇 为溶剂, 30.0 ℃ 、310.27 kPa 条件下, 反应 3.0h, 以97%的产率得到methyl (3α-aminomethyl)-3β,7α,12α-trihydroxy-5β-cholan-24-oate
    参考文献:
    名称:
    Design and synthesis of bile acid-based amino sterols as antimicrobial agents
    摘要:
    New bile acid-based amino sterols were synthesized in good yields from C-3 beta-oxiranes as key intermediates. These derivatives were evaluated for their in vitro antimicrobial properties against human pathogens. These compounds showed better antibacterial activity as compared to antifungal activity. Compounds 21 and 22 showed comparable antibacterial activity to gentamicin against Staphylococcus aureus with IC50 values of 5.14 and 4.46 mu g/mL. This is the first report for the synthesis of C-3 beta-oxiranes on the steroids having A/B cis ring junction and these oxiranes have been used for the synthesis of amino sterols 17, 18, 21, and 22. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.07.117
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文献信息

  • Design and synthesis of bile acid-based amino sterols as antimicrobial agents
    作者:Nilkanth G. Aher、Vandana S. Pore、Nripendra N. Mishra、Praveen K. Shukla、Rajesh G. Gonnade
    DOI:10.1016/j.bmcl.2009.07.117
    日期:2009.9
    New bile acid-based amino sterols were synthesized in good yields from C-3 beta-oxiranes as key intermediates. These derivatives were evaluated for their in vitro antimicrobial properties against human pathogens. These compounds showed better antibacterial activity as compared to antifungal activity. Compounds 21 and 22 showed comparable antibacterial activity to gentamicin against Staphylococcus aureus with IC50 values of 5.14 and 4.46 mu g/mL. This is the first report for the synthesis of C-3 beta-oxiranes on the steroids having A/B cis ring junction and these oxiranes have been used for the synthesis of amino sterols 17, 18, 21, and 22. (C) 2009 Elsevier Ltd. All rights reserved.
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