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3-(5,7-dioxo-3,7-dihydro-2H-thiazolo<3,2-c>pyrimidin-6-yl)-2-methylpropionitrile

中文名称
——
中文别名
——
英文名称
3-(5,7-dioxo-3,7-dihydro-2H-thiazolo<3,2-c>pyrimidin-6-yl)-2-methylpropionitrile
英文别名
3-(5,7-Dioxo-2,3-dihydro-[1,3]thiazolo[3,2-c]pyrimidin-6-yl)-2-methylpropanenitrile
3-(5,7-dioxo-3,7-dihydro-2H-thiazolo<3,2-c>pyrimidin-6-yl)-2-methylpropionitrile化学式
CAS
——
化学式
C10H11N3O2S
mdl
——
分子量
237.282
InChiKey
SYBFOVIINQFXPV-UHFFFAOYSA-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):
    0.1
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    89.7
  • 氢给体数:
    0
  • 氢受体数:
    4

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

  • 作为产物:
    参考文献:
    名称:
    A new class of potent hypolipemic agents raising high-density lipoproteins. Synthesis, reactions and pharmacological properties
    摘要:
    A series of thiazolo[3,2-c]pyrimidin-5,7-diones has been synthesized. Results from in vivo evaluations in rats have shown that many of these compounds produce a pronounced increase of HDL cholesterol and a marked decrease of LDL and VLDL cholesterol. The most potent compound 17 (30 mg/kg/d per os over 7 d in male rats) led to the following changes: HDL cholesterol + 101%, LDL cholesterol -40%, and VLDL cholesterol -98%. These effects may result in antiatherosclerotic properties in these compounds. The preparation of 7-amino-2,3-dihydrothiazolo[3,2-a]pyrimidin-5-ones and 5-amino-2,3-dihydrothiazolo[3,2-a] pyrimidin-7-ones is described.
    DOI:
    10.1016/0223-5234(94)90105-8
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文献信息

  • A new class of potent hypolipemic agents raising high-density lipoproteins. Synthesis, reactions and pharmacological properties
    作者:H FURRER、E GRANZER、R WAGNER
    DOI:10.1016/0223-5234(94)90105-8
    日期:——
    A series of thiazolo[3,2-c]pyrimidin-5,7-diones has been synthesized. Results from in vivo evaluations in rats have shown that many of these compounds produce a pronounced increase of HDL cholesterol and a marked decrease of LDL and VLDL cholesterol. The most potent compound 17 (30 mg/kg/d per os over 7 d in male rats) led to the following changes: HDL cholesterol + 101%, LDL cholesterol -40%, and VLDL cholesterol -98%. These effects may result in antiatherosclerotic properties in these compounds. The preparation of 7-amino-2,3-dihydrothiazolo[3,2-a]pyrimidin-5-ones and 5-amino-2,3-dihydrothiazolo[3,2-a] pyrimidin-7-ones is described.
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