1-[2-(4-Chloro-phenoxy)-ethylamino]-3-phenoxy-propan-2-ol | 64463-72-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 1-[2-(4-Chloro-phenoxy)-ethylamino]-3-phenoxy-propan-2-ol
• 英文别名: 1-[2-(4-Chlorophenoxy)ethylamino]-3-phenoxypropan-2-ol
• CAS: 64463-72-5
• 化学式: C₁₇H₂₀ClNO₃
• 分子量: 321.804
• InChiKey: YEDABNPBABJIET-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  22
• 可旋转键数：
  9
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  50.7
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  苯基缩水甘油醚 、 2-(4-chlorophenoxy)ethan-1-amine hydrochloride 在 sodium hydroxide 作用下， 以 丙醇 为溶剂， 生成 1-[2-(4-Chloro-phenoxy)-ethylamino]-3-phenoxy-propan-2-ol
  参考文献：
  名称：

  .beta.-Adrenergic blocking agents. 17. 1-Phenoxy-3-phenoxyalkylamino-2-propanols and 1-alkoxyalkylamino-3-phenoxy-2-propanols

  摘要：

  The synthesis is described of a series of derivatives of 1-phenoxy-3-phenoxyalkylamino-2-propanols and 1-alkoxyalkylamino-3-phenoxy-2-propranols. The compounds were investigated for their beta-adrenoceptor blocking properties and many showed a surprising degree of cardioselectivity when tested in vivo in anesthetized cats for their effects on an isoproterenol-induced tachycardia and depressor response. The structure-activity relationship shown by this series of compounds is related to that of known cardioselective analogues and a possible reason for their cardioselectivity is discussed.

  DOI：

  10.1021/jm00222a022

文献信息

• Lehmann; Eckardt; Faust, Pharmazie, 1980, vol. 35, # 5-6, p. 278 - 284
  作者：Lehmann、Eckardt、Faust、Fiedler

  DOI：——

  日期：——
• LEHMANN D.; ECKARDT R.; FAUST G.; FIEDLER W., PHARMAZIE, 1980, 35, NO 5-6, 278-284
  作者：LEHMANN D.、 ECKARDT R.、 FAUST G.、 FIEDLER W.

  DOI：——

  日期：——
• US6051605A
  申请人：——

  公开号：US6051605A

  公开（公告）日：2000-04-18
• .beta.-Adrenergic blocking agents. 17. 1-Phenoxy-3-phenoxyalkylamino-2-propanols and 1-alkoxyalkylamino-3-phenoxy-2-propanols
  作者：L. H. Smith、H. Tucker

  DOI：10.1021/jm00222a022

  日期：1977.12

  The synthesis is described of a series of derivatives of 1-phenoxy-3-phenoxyalkylamino-2-propanols and 1-alkoxyalkylamino-3-phenoxy-2-propranols. The compounds were investigated for their beta-adrenoceptor blocking properties and many showed a surprising degree of cardioselectivity when tested in vivo in anesthetized cats for their effects on an isoproterenol-induced tachycardia and depressor response. The structure-activity relationship shown by this series of compounds is related to that of known cardioselective analogues and a possible reason for their cardioselectivity is discussed.