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2-imino-3-(3-chloro-4-methoxy-3-nitrobenzoylmethyl)thiazoline hydrobromide | 145235-74-1

中文名称
——
中文别名
——
英文名称
2-imino-3-(3-chloro-4-methoxy-3-nitrobenzoylmethyl)thiazoline hydrobromide
英文别名
——
2-imino-3-(3-chloro-4-methoxy-3-nitrobenzoylmethyl)thiazoline hydrobromide化学式
CAS
145235-74-1
化学式
BrH*C12H13N3O4S
mdl
——
分子量
376.231
InChiKey
SIXHRETYAPPZJC-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):
    2.35
  • 重原子数:
    21.0
  • 可旋转键数:
    5.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    96.53
  • 氢给体数:
    1.0
  • 氢受体数:
    6.0

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Synthesis and anti-filarial activity of 6-(3-aminophenyl)-2,3,5,6-tetrahydroimidazol[2,1-b]thiazole derivatives
    摘要:
    Structure-activity studies against filariae are described for a series of derivatives of 6-(3-aminophenyl)-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole (15) derivatives. In an in vivo assay using gerbils implanted with both Acanthocheilonema viteae and Brugia pahangi, the former parasite was shown to be the more sensitive to a range of amides of 15. None of these compounds, however, had any activity at 5 x 10(-5) mol against the worms in vitro suggesting that they required in vivo activation. This was confirmed when the benzamido derivative (6) was shown to be rapidly metabolised in gerbils to the parent amine (15). The latter had potent effects on filariae both in vivo and in vitro but was also found to be toxic to mammals and unsuitable for further development. Unsuccessful attempts to improve upon the therapeutic index of 15 through the synthesis of various novel analogues are described.
    DOI:
    10.1016/0223-5234(92)90184-3
  • 作为产物:
    参考文献:
    名称:
    Synthesis and anti-filarial activity of 6-(3-aminophenyl)-2,3,5,6-tetrahydroimidazol[2,1-b]thiazole derivatives
    摘要:
    Structure-activity studies against filariae are described for a series of derivatives of 6-(3-aminophenyl)-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole (15) derivatives. In an in vivo assay using gerbils implanted with both Acanthocheilonema viteae and Brugia pahangi, the former parasite was shown to be the more sensitive to a range of amides of 15. None of these compounds, however, had any activity at 5 x 10(-5) mol against the worms in vitro suggesting that they required in vivo activation. This was confirmed when the benzamido derivative (6) was shown to be rapidly metabolised in gerbils to the parent amine (15). The latter had potent effects on filariae both in vivo and in vitro but was also found to be toxic to mammals and unsuitable for further development. Unsuccessful attempts to improve upon the therapeutic index of 15 through the synthesis of various novel analogues are described.
    DOI:
    10.1016/0223-5234(92)90184-3
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