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methyl (3R,10S)-3-hydroxy-8,10,19-trimethyltricosanoate | 1160038-93-6

中文名称
——
中文别名
——
英文名称
methyl (3R,10S)-3-hydroxy-8,10,19-trimethyltricosanoate
英文别名
——
methyl (3R,10S)-3-hydroxy-8,10,19-trimethyltricosanoate化学式
CAS
1160038-93-6
化学式
C27H54O3
mdl
——
分子量
426.724
InChiKey
NCLSCMWMTUKHMB-DOWAUTBPSA-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):
    8.08
  • 重原子数:
    30.0
  • 可旋转键数:
    21.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.96
  • 拓扑面积:
    46.53
  • 氢给体数:
    1.0
  • 氢受体数:
    3.0

反应信息

  • 作为反应物:
    描述:
    methyl (3R,10S)-3-hydroxy-8,10,19-trimethyltricosanoate(R)-methoxytrifluoromethylphenylacetyl chloride吡啶4-二甲氨基吡啶 作用下, 反应 1.0h, 以0.5 mg的产率得到methyl (3R,10S)-8,10,19-trimethyl-3-(((S)-3,3,3-trifluoro-2-methoxy-2-phenylpropanoyl)oxy)tricosanoate
    参考文献:
    名称:
    Biselyngbyaside, a Macrolide Glycoside from the Marine Cyanobacterium Lyngbya sp.
    摘要:
    Bioassay-guided fractionation of the cytotoxic constituents of the marine cyanobacterium Lyngbya sp. led to the isolation of biselyngbyaside (1), a new 18-membered macrolide glycoside. The structure of I was established by spectroscopic analysis including 2D-NMR techniques and by synthetic studies. Biselyngbyaside (1) exhibits broad-spectrum cytotoxicity in a human tumor cell line panel.
    DOI:
    10.1021/ol900579k
  • 作为产物:
    描述:
    甲醇biselyngbyaside 在 10% palladium on carbon 、 氢气盐酸 作用下, 以 乙醇甲醇 为溶剂, 反应 50.0h, 以25%的产率得到methyl (3R,10S)-3-hydroxy-8,10,19-trimethyltricosanoate
    参考文献:
    名称:
    Biselyngbyaside, a Macrolide Glycoside from the Marine Cyanobacterium Lyngbya sp.
    摘要:
    Bioassay-guided fractionation of the cytotoxic constituents of the marine cyanobacterium Lyngbya sp. led to the isolation of biselyngbyaside (1), a new 18-membered macrolide glycoside. The structure of I was established by spectroscopic analysis including 2D-NMR techniques and by synthetic studies. Biselyngbyaside (1) exhibits broad-spectrum cytotoxicity in a human tumor cell line panel.
    DOI:
    10.1021/ol900579k
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