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prostaglandin A2 1,3-bis(nitrooxy)prop-2-yl ester | 189940-87-2

中文名称
——
中文别名
——
英文名称
prostaglandin A2 1,3-bis(nitrooxy)prop-2-yl ester
英文别名
——
prostaglandin A2 1,3-bis(nitrooxy)prop-2-yl ester化学式
CAS
189940-87-2
化学式
C23H34N2O10
mdl
——
分子量
498.53
InChiKey
GIUFGXJKFLIXQE-DOLBRABKSA-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):
    3.3
  • 重原子数:
    35.0
  • 可旋转键数:
    19.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.65
  • 拓扑面积:
    168.34
  • 氢给体数:
    1.0
  • 氢受体数:
    10.0

反应信息

  • 作为反应物:
    描述:
    prostaglandin A2 1,3-bis(nitrooxy)prop-2-yl ester双氧水 、 potassium hydroxide 作用下, 生成 10,11-epoxy-PGA2
    参考文献:
    名称:
    1,3-Dinitrates of cyclooxygenase metabolites of endocannabinoid 2-arachidonoylglycerol. Synthesis and properties
    摘要:
    The 1,3-Dinitrates of glycerol esters of natural prostaglandins that are the cyclooxygenase metabolites of 2-arachidonoylglycerol, an endogenous ligand of cannabinoid receptors, were synthesized for the first time. Four methods of synthesis of these esters were developed via the activation of a carboxyl group and their chemical and pharmacological properties were investigated. The esters exhibit a more selective pharmacological spectrum of activities in comparison with the corresponding natural prostaglandins: some types of myotropic activity were enhanced, while others were loosened. 1,3-dinitroglycerol esters act as vasodilators, whereas the majority of natural prostaglandins act as vasoconstrictors. The observed changes result from the introduction of an NO-releasing fragment into prostaglandin molecule.
    DOI:
    10.1134/s1068162009020113
  • 作为产物:
    描述:
    盐酸 作用下, 以 甲醇 为溶剂, 反应 0.33h, 以123.8 mg的产率得到prostaglandin A2 1,3-bis(nitrooxy)prop-2-yl ester
    参考文献:
    名称:
    Prostaglandin fluorides in synthesis of natural prostaglandin derivatives at carboxyl group
    摘要:
    Methods of synthesis of prostaglandin fluorides were developed and their properties were investigated. These compounds were shown to be convenient synthetic precursors for obtaining esters and amides of natural prostaglandins and their fluorodeoxy analogues.
    DOI:
    10.1134/s1068162009010142
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