2,2,2-trichloro-N'-[2-(4-hydroxyphenyl)ethyl]ethanimidamide | 60523-50-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 酚类
• 英文名称: 2,2,2-trichloro-N'-[2-(4-hydroxyphenyl)ethyl]ethanimidamide
• CAS: 60523-50-4
• 化学式: C₁₀H₁₁Cl₃N₂O
• 分子量: 281.569
• InChiKey: NPJDADMARPRANJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  58.6
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  酪胺盐酸盐 、 三氯乙腈 在 三乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 2,2,2-trichloro-N'-[2-(4-hydroxyphenyl)ethyl]ethanimidamide
  参考文献：
  名称：

  Trichloroacetamidines, a new class of positive inotropic agents

  摘要：

  A series of trichloroacetamidine derivatives, obtained by addition of amines to trichloroacetonitrile, was evaluated for positive inotropic activity on isolated cat heart papillary muscles. Increased contractility, not antagonized by beta-adrenergic blockade with sotalol or reserpine pretreatment, was observed in this assay with a variety of N-substituted trichloroacetamidine derivatives. More extensive pharmacological studies with the 3-indolylmethyl analogue 2 showed that this amidine in dogs, 5 mg/kg iv, produced a positive inotropic effect more pronounced than that of ouabain, 50 microgram/kg iv. Several of the trichloroacetamidines were found to be inhibitors of guinea pig kidney and calf heart Na-K-dependent ATPase and to have specificity for these enzymes different from that of ouabain. Bacterial mutagenic activity was observed with three members, 2,3, and 12, of the series.

  DOI：

  10.1021/jm00210a021

文献信息

• SAARI W. S.; FREEDMAN M. B.; HUFF J. R.; KING S. W.; RAAB A. W.; BERGSTRA+, J. MED. CHEM., 1978, 21, NO 12, 1283-1290
  作者：SAARI W. S.、 FREEDMAN M. B.、 HUFF J. R.、 KING S. W.、 RAAB A. W.、 BERGSTRA+

  DOI：——

  日期：——
• Trichloroacetamidines, a new class of positive inotropic agents
  作者：Walfred S. Saari、Mark B. Freedman、Joel R. Huff、Stella W. King、Andrew W. Raab、Susan J. Bergstrand、Edward L. Engelhardt、Alexander Scriabine、George Morgan

  DOI：10.1021/jm00210a021

  日期：1978.12

  A series of trichloroacetamidine derivatives, obtained by addition of amines to trichloroacetonitrile, was evaluated for positive inotropic activity on isolated cat heart papillary muscles. Increased contractility, not antagonized by beta-adrenergic blockade with sotalol or reserpine pretreatment, was observed in this assay with a variety of N-substituted trichloroacetamidine derivatives. More extensive pharmacological studies with the 3-indolylmethyl analogue 2 showed that this amidine in dogs, 5 mg/kg iv, produced a positive inotropic effect more pronounced than that of ouabain, 50 microgram/kg iv. Several of the trichloroacetamidines were found to be inhibitors of guinea pig kidney and calf heart Na-K-dependent ATPase and to have specificity for these enzymes different from that of ouabain. Bacterial mutagenic activity was observed with three members, 2,3, and 12, of the series.