(2,4-Dihydroxy-3-propyl-phenyl)-pyridin-4-yl-methanone | 183013-71-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (2,4-Dihydroxy-3-propyl-phenyl)-pyridin-4-yl-methanone
• CAS: 183013-71-0
• 化学式: C₁₅H₁₅NO₃
• 分子量: 257.289
• InChiKey: SDXLTAZXFCGLGY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.68
• 重原子数：
  19.0
• 可旋转键数：
  4.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  70.42
• 氢给体数：
  2.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  (2,4-Dihydroxy-3-propyl-phenyl)-pyridin-4-yl-methanone 在 sodium acetate 、 potassium carbonate 、 溶剂黄146 、 potassium iodide 作用下， 以 丁酮 为溶剂， 生成 (5Z)-5-[[4-[[3-hydroxy-2-propyl-4-(pyridine-4-carbonyl)phenoxy]methyl]phenyl]methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one
  参考文献：
  名称：

  Synthesis and structure-activity relationships of benzophenones as inhibitors of cathepsin D

  摘要：

  Non peptide inhibitors of cathepsin D, an aspartyl protease that has been implicated in many disease states including Alzheimer's disease, were prepared and evaluated. The most potent inhibitor of cathepsin D in this series was found to be (Z)-5-[[4-(4-benzoyl-3-hydroxy-2-propylphenoxy)methylphenyl]methylene]-2-thioxo-4-thiazolidinone (3f, IC50 = 210 nM). Copyright (C) 1996 Elsevier Science Ltd

  DOI：

  10.1016/0960-894x(96)00393-9
• 作为产物：
  描述：

  异烟酸酰氯 、 2-正丙基间苯二酚 在 三氯化铝 作用下， 以 二氯甲烷 为溶剂， 生成 (2,4-Dihydroxy-3-propyl-phenyl)-pyridin-4-yl-methanone
  参考文献：
  名称：

  Synthesis and structure-activity relationships of benzophenones as inhibitors of cathepsin D

  摘要：

  Non peptide inhibitors of cathepsin D, an aspartyl protease that has been implicated in many disease states including Alzheimer's disease, were prepared and evaluated. The most potent inhibitor of cathepsin D in this series was found to be (Z)-5-[[4-(4-benzoyl-3-hydroxy-2-propylphenoxy)methylphenyl]methylene]-2-thioxo-4-thiazolidinone (3f, IC50 = 210 nM). Copyright (C) 1996 Elsevier Science Ltd

  DOI：

  10.1016/0960-894x(96)00393-9