2-<<3-(3-pyridinylmethoxy)phenyl>methylene>hydrazinecarboximidamide

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 2-<<3-(3-pyridinylmethoxy)phenyl>methylene>hydrazinecarboximidamide
• 英文别名: 2-{[3-(3-pyridinylmethoxy)phenyl]methylene}hydrazinecarboximidamide；2-[(E)-[3-(pyridin-3-ylmethoxy)phenyl]methylideneamino]guanidine
• 化学式: C₁₄H₁₅N₅O
• 分子量: 269.306
• InChiKey: LLRUHBOJZJPNOE-GIJQJNRQSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.9
• 重原子数：
  20
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  98.9
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  3-吡啶甲醇 在 氢溴酸 、 三苯基膦 、 偶氮二甲酸二乙酯 作用下， 以 四氢呋喃 、 乙醇 为溶剂， 反应 23.5h， 生成 2-<<3-(3-pyridinylmethoxy)phenyl>methylene>hydrazinecarboximidamide
  参考文献：
  名称：

  Guanabenz-related amidinohydrazones: potent non-azole inhibitors of aldosterone biosynthesis

  摘要：

  A new series of potent, guanabenz-derived, non-steroidal aldosterone biosynthesis inhibitors are presented. Salient features of the structure-activity relationship indicate the requirement of a hydrophobic core, presence of a hydrophilic (or basic) peripheral appendage, and, in some cases, profound dependence on hydrazone stereochemistry. The most potent compound of the series, 29, was 2 orders of magnitude more potent than guanabenz as an aldosterone biosynthesis inhibitor.

  DOI：

  10.1016/0223-5234(94)90040-x

文献信息

• Guanabenz-related amidinohydrazones: potent non-azole inhibitors of aldosterone biosynthesis
  作者：RM Soll、PJ Dollings、RD Mitchell、DA Hafner

  DOI：10.1016/0223-5234(94)90040-x

  日期：1994.1

  A new series of potent, guanabenz-derived, non-steroidal aldosterone biosynthesis inhibitors are presented. Salient features of the structure-activity relationship indicate the requirement of a hydrophobic core, presence of a hydrophilic (or basic) peripheral appendage, and, in some cases, profound dependence on hydrazone stereochemistry. The most potent compound of the series, 29, was 2 orders of magnitude more potent than guanabenz as an aldosterone biosynthesis inhibitor.