<4-Chlorphenoxy>-acetimidsaeureethylester | 3598-09-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: <4-Chlorphenoxy>-acetimidsaeureethylester
• 英文别名: Ethyl 2-(4-chlorophenoxy)ethanimidate
• CAS: 3598-09-2
• 化学式: C₁₀H₁₂ClNO₂
• 分子量: 213.664
• InChiKey: BIWUKZKQOFMJNH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  14
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  42.3
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3,4-二氨基吡啶 、 <4-Chlorphenoxy>-acetimidsaeureethylester 以28%的产率得到
  参考文献：
  名称：

  GLOZMAN, O. M.;ORLOVA, EH. K.;MESHCHERYAKOVA, L. M.;VORONINA, T. A.;GARIB+, XIM.-FARMATS. ZH., 23,(1989) N, S. 916-918

  摘要：

  DOI：
• 作为产物：
  描述：

  乙醇 、 4-氯苯氧基乙腈 在 盐酸 作用下， 生成 <4-Chlorphenoxy>-acetimidsaeureethylester
  参考文献：
  名称：

  Zida,P.; Viout,P., Bulletin de la Societe Chimique de France, 1965, p. 2309 - 2314

  摘要：

  DOI：

文献信息

• 4,5-Dihydro-1-phenyl-1H-2,4-benzodiazepines: Novel antiarrhythmic agents
  作者：Robert E. Johnson、Eugene R. Baizman、Carolyn Becker、Eric A. Bohnet、Rebecca H. Bell、Nancy C. Birsner、Carl A. Busacca、Philip M. Carabateas、Christopher C. Chadwick

  DOI：10.1021/jm00074a017

  日期：1993.10

  A series of 4,5-dihydro-1-phenyl-1H-2,4-benzodiazepines has been identified as potential antiarrhythmic agents that interact with sodium and potassium channels and prolong the ventricular effective refractory period (ERP) in anesthetized guinea pigs. Concomitant displacement of radiolabeled bactrachotoxin from site II in Na+ channels and of radiolabeled dofetilide from delayed rectifier K+ channels was evident with all members of this chemical series at a concentration of 10 muM. Structure-activity relationship (SAR) studies using a paced guinea pig model to assess prolongation of the ERP indicated that methyl or ethyl at the 1-position had little effect on activity, while larger groups caused a diminution of activity. Compounds with substituents at either the 3- or 4-position that increased lipophilicity generally were more potent; however, too many lipophilic substituents simultaneously at positions 1, 3, and 4 resulted in less active compounds. Substituents on either aromatic ring had little influence on activity, and phenyl at the 5-position resulted in a significant reduction in antiarrhythmic activity. When two sets of enantiomerically pure compounds were tested in the guinea pig, chirality was shown to be important for activity of 8, where the (R)-enantiomer was the more active, but not in the case of 15, where the enantiomers were equiactive. Several compounds in this series increased the threshold for vertricular fibrillation and refractoriness in myocardially-infarcted anesthetized cata and delayed the onset of aconitine-induced arrhythmias in anesthetized guinea pigs following intravenous dosing. Moreover, these compounds possessed oral antiarrhythmic activity in conscious myocardially-infarcted dogs. Compound R-15 has been advanced for further biological and toxicological evaluations.