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methyl (6S)-6-[(2S,3S,4R,5S,6R,8R,9R,10R)-10-[(2R,4S,5S,6S)-4,5-dihydroxy-6-methyloxan-2-yl]oxy-9-ethyl-4-hydroxy-3,5,8-trimethyl-1,7-dioxaspiro[5.5]undecan-2-yl]heptanoate | 129608-39-5

中文名称
——
中文别名
——
英文名称
methyl (6S)-6-[(2S,3S,4R,5S,6R,8R,9R,10R)-10-[(2R,4S,5S,6S)-4,5-dihydroxy-6-methyloxan-2-yl]oxy-9-ethyl-4-hydroxy-3,5,8-trimethyl-1,7-dioxaspiro[5.5]undecan-2-yl]heptanoate
英文别名
——
methyl (6S)-6-[(2S,3S,4R,5S,6R,8R,9R,10R)-10-[(2R,4S,5S,6S)-4,5-dihydroxy-6-methyloxan-2-yl]oxy-9-ethyl-4-hydroxy-3,5,8-trimethyl-1,7-dioxaspiro[5.5]undecan-2-yl]heptanoate化学式
CAS
129608-39-5;129705-07-3
化学式
C28H50O9
mdl
——
分子量
530.7
InChiKey
SQIPJUXDHQQORO-WUXLQDHASA-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):
    3.6
  • 重原子数:
    37
  • 可旋转键数:
    10
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.96
  • 拓扑面积:
    124
  • 氢给体数:
    3
  • 氢受体数:
    9

反应信息

  • 作为反应物:
    描述:
    methyl (6S)-6-[(2S,3S,4R,5S,6R,8R,9R,10R)-10-[(2R,4S,5S,6S)-4,5-dihydroxy-6-methyloxan-2-yl]oxy-9-ethyl-4-hydroxy-3,5,8-trimethyl-1,7-dioxaspiro[5.5]undecan-2-yl]heptanoatesodium hydroxide 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 生成 (S)-6-[(2S,3S,4R,5S,6R,8R,9R,10R)-10-((2R,4S,5S,6S)-4,5-Dihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-9-ethyl-4-hydroxy-3,5,8-trimethyl-1,7-dioxa-spiro[5.5]undec-2-yl]-heptanoic acid
    参考文献:
    名称:
    Secondary Metabolites by Chemical Screening 14. Transformation of Elaiophylin in subunits of Naturally Occurring Acid Ionophores: Synthesis, Anticoccidial Activity and Studies Concerning the Ionophoric Properties
    摘要:
    The synthesis of the polyether subunits (8 - 11), starting from elaiophylin (1), as well as their biological properties, nmr spectra and conformational studies were described and discussed. Based upon the missing ability of potassium transport it was deduced that compounds (8 - 11) were new lead structures concerning their anticoccidial activity.
    DOI:
    10.3987/com-91-5778
  • 作为产物:
    参考文献:
    名称:
    Secondary Metabolites by Chemical Screening 14. Transformation of Elaiophylin in subunits of Naturally Occurring Acid Ionophores: Synthesis, Anticoccidial Activity and Studies Concerning the Ionophoric Properties
    摘要:
    The synthesis of the polyether subunits (8 - 11), starting from elaiophylin (1), as well as their biological properties, nmr spectra and conformational studies were described and discussed. Based upon the missing ability of potassium transport it was deduced that compounds (8 - 11) were new lead structures concerning their anticoccidial activity.
    DOI:
    10.3987/com-91-5778
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文献信息

  • Secondary Metabolites by Chemical Screening 14. Transformation of Elaiophylin in subunits of Naturally Occurring Acid Ionophores: Synthesis, Anticoccidial Activity and Studies Concerning the Ionophoric Properties
    作者:Peter Hammann、Gerhard Kretzschmar、Robert Klein、Maria Kajtár-Peredy、Achim Kröger、Frank Ditzel、Wolfgang Raether
    DOI:10.3987/com-91-5778
    日期:——
    The synthesis of the polyether subunits (8 - 11), starting from elaiophylin (1), as well as their biological properties, nmr spectra and conformational studies were described and discussed. Based upon the missing ability of potassium transport it was deduced that compounds (8 - 11) were new lead structures concerning their anticoccidial activity.
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