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2,5-bis-[2-(5-amidino-pyridyl)]thiophene | 1143621-41-3

中文名称
——
中文别名
——
英文名称
2,5-bis-[2-(5-amidino-pyridyl)]thiophene
英文别名
6-[5-(5-Carbamimidoylpyridin-2-yl)thiophen-2-yl]pyridine-3-carboximidamide
2,5-bis-[2-(5-amidino-pyridyl)]thiophene化学式
CAS
1143621-41-3
化学式
C16H14N6S
mdl
——
分子量
322.393
InChiKey
KMPJUMXTLPNRDN-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):
    0.8
  • 重原子数:
    23
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    154
  • 氢给体数:
    4
  • 氢受体数:
    5

文献信息

  • 2,5-DIARYL SELENOPHENE COMPOUNDS, AZA 2,5-DIARYL THIOPHENE COMPOUNDS, AND THEIR PRODRUGS AS ANTIPROTOZOAL AGENTS
    申请人:Tidwell Richard R.
    公开号:US20100331368A1
    公开(公告)日:2010-12-30
    Novel dicationic 2,5-diaryl selenophene compounds are described. Also described are novel aza analogues of dicationic 2,5-diaryl thiophenes. The presently disclosed dicationic compounds exhibit in vitro activity versus Trypanosoma brucei rhodesiense, Plasmodium falciparum , and/or Leishmania donovani comparable to that of pentamidine and furamidine. Some of the novel dicationic compounds display good activity in vivo in a murine model of a Trypanosoma brucei rhodesiense infection.
    本文描述了新型二阳离子2,5-二芳基吡咯烷化合物。同时,还描述了新型二阳离子2,5-二芳基噻吩的氮杂环类似物。目前披露的二阳离子化合物在体外对Trypanosoma brucei rhodesiense、Plasmodium falciparum和/或Leishmania donovani表现出与Pentamidine和Furamidine相当的活性。其中一些新型二阳离子化合物在Trypanosoma brucei rhodesiense感染的小鼠模型中表现出良好的体内活性。
  • [EN] 2,5-DIARYL SELENOPHENE COMPOUNDS, AZA 2,5-DIARYL THIOPHENE COMPOUNDS, AND THEIR PRODRUGS AS ANTIPROTOZOAL AGENTS<br/>[FR] COMPOSÉS DE 2,5-DIARYLSÉLÉNOPHÈNE, COMPOSÉS D'AZA-2,5-DIARYLTHIOPHÈNE ET LEURS PROMÉDICAMENTS UTILISÉS EN TANT QU'AGENTS ANTIPROTOZOAIRES
    申请人:UNIV NORTH CAROLINA
    公开号:WO2009051796A2
    公开(公告)日:2009-04-23
    Novel dicationic 2,5-diaryl selenophene compounds are described. Also described are novel aza analogues of dicationic 2,5-diaryl thiophenes. The presently disclosed dicationic compounds exhibit in vitro activity versus Trypanosoma brucei rhodesiense, Plasmodium falciparum, and/or Leishmania donovani comparable to that of pentamidine and furamidine. Some of the novel dicationic compounds display good activity in vivo in a murine model of a Trypanosoma brucei rhodesiense infection.
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