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6-(2-imidazolin-2-ylamino)-2H-1,4-benzoxazin-3(4H)-one hydroiodide | 120711-66-2

中文名称
——
中文别名
——
英文名称
6-(2-imidazolin-2-ylamino)-2H-1,4-benzoxazin-3(4H)-one hydroiodide
英文别名
7-(4,5-dihydro-1H-imidazol-2-ylamino)-4H-1,4-benzoxazin-3-one;hydroiodide
6-(2-imidazolin-2-ylamino)-2H-1,4-benzoxazin-3(4H)-one hydroiodide化学式
CAS
120711-66-2
化学式
C11H12N4O2*HI
mdl
——
分子量
360.154
InChiKey
XKJYYQCMGKODAP-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):
    1.01
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    74.8
  • 氢给体数:
    4
  • 氢受体数:
    3

反应信息

  • 作为产物:
    参考文献:
    名称:
    Heteroaromatic analogs of the .alpha.2-adrenoreceptor partial agonist clonidine
    摘要:
    A 1,4-dioxane analogue (1) of the alpha 2-adrenoreceptor partial agonist clonidine (2) has previously been shown to possess an interesting but complex pharmacological profile. In this study, from a series of other heterocyclic analogues of clonidine, the 1,4-oxazines 6 and 12 were found to resemble 1 in that they are partial alpha 2-agonists in the periphery and are excluded from the central nervous system. However, when given directly into the brain, they behave as pure alpha 2-antagonists.
    DOI:
    10.1021/jm00127a037
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文献信息

  • Heteroaromatic analogs of the .alpha.2-adrenoreceptor partial agonist clonidine
    作者:Christopher B. Chapleo、Richard C. M. Butler、David C. England、Peter L. Myers、Alan G. Roach、Colin F. C. Smith、Michael R. Stillings、Ian F. Tulloch
    DOI:10.1021/jm00127a037
    日期:1989.7
    A 1,4-dioxane analogue (1) of the alpha 2-adrenoreceptor partial agonist clonidine (2) has previously been shown to possess an interesting but complex pharmacological profile. In this study, from a series of other heterocyclic analogues of clonidine, the 1,4-oxazines 6 and 12 were found to resemble 1 in that they are partial alpha 2-agonists in the periphery and are excluded from the central nervous system. However, when given directly into the brain, they behave as pure alpha 2-antagonists.
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