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4-(4-Chloro-phenyl)-piperazine-1-carbothioic acid [1-pyridin-2-yl-eth-(E)-ylidene]-hydrazide | 132856-23-6

中文名称
——
中文别名
——
英文名称
4-(4-Chloro-phenyl)-piperazine-1-carbothioic acid [1-pyridin-2-yl-eth-(E)-ylidene]-hydrazide
英文别名
4-(4-chlorophenyl)-N-(1-pyridin-2-ylethylideneamino)piperazine-1-carbothioamide
4-(4-Chloro-phenyl)-piperazine-1-carbothioic acid [1-pyridin-2-yl-eth-(E)-ylidene]-hydrazide化学式
CAS
132856-23-6
化学式
C18H20ClN5S
mdl
——
分子量
373.909
InChiKey
VXFXOMIPECTEAW-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):
    3.16
  • 重原子数:
    25.0
  • 可旋转键数:
    3.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    43.76
  • 氢给体数:
    1.0
  • 氢受体数:
    4.0

反应信息

  • 作为产物:
    描述:
    1-(4-氯苯基)哌嗪3-[1-(2-pyridyl)ethylidene]hydrazinecarbodithioate乙醇 为溶剂, 反应 24.0h, 以60%的产率得到4-(4-Chloro-phenyl)-piperazine-1-carbothioic acid [1-pyridin-2-yl-eth-(E)-ylidene]-hydrazide
    参考文献:
    名称:
    2-Acetylpyridine thiosemicarbazones. 13. Derivatives with antifilarial activity
    摘要:
    Several members of a series of 2-acetylpyridine thiosemicarbazones possess in vivo and in vitro macrofilaricidal properties. The most promising of the group tested is N4-(2-aminophenyl)-2-[1-(2-pyridinyl)ethylidene]-hydrazinecarbothioamide (4), which suppressed 100% of the macrofilariae of Brugia pahangi and 94% of those of Acanthocheilonema viteae in the jird at a dose of 25 mg/kg per day x 5. Compounds 4 and 14 were also shown to inactivate or kill Onchocerca gutturosa and Onchocerca volvulus adult worms as measured by the loss of their motility or the inhibition of the conversion by the worms of the dye MTT to formazan.
    DOI:
    10.1021/jm00108a027
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文献信息

  • 2-Acetylpyridine thiosemicarbazones. 13. Derivatives with antifilarial activity
    作者:Daniel L. Klayman、Ai J. Lin、John W. McCall、Shao Yin Wang、Simon Townson、Max Grogl、Kenneth E. Kinnamon
    DOI:10.1021/jm00108a027
    日期:1991.4
    Several members of a series of 2-acetylpyridine thiosemicarbazones possess in vivo and in vitro macrofilaricidal properties. The most promising of the group tested is N4-(2-aminophenyl)-2-[1-(2-pyridinyl)ethylidene]-hydrazinecarbothioamide (4), which suppressed 100% of the macrofilariae of Brugia pahangi and 94% of those of Acanthocheilonema viteae in the jird at a dose of 25 mg/kg per day x 5. Compounds 4 and 14 were also shown to inactivate or kill Onchocerca gutturosa and Onchocerca volvulus adult worms as measured by the loss of their motility or the inhibition of the conversion by the worms of the dye MTT to formazan.
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