17-(3,3-dimethylbutyryl)-4-nor-3,5-seco-5-oxo-17-azaandrostan-3-oic acid | 182277-90-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 17-(3,3-dimethylbutyryl)-4-nor-3,5-seco-5-oxo-17-azaandrostan-3-oic acid
• CAS: 182277-90-3
• 化学式: C₂₃H₃₇NO₄
• 分子量: 391.551
• InChiKey: MQFPWPVJWMLYIB-NPABLSHVSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.29
• 重原子数：
  28.0
• 可旋转键数：
  4.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.87
• 拓扑面积：
  74.68
• 氢给体数：
  1.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  17-(3,3-dimethylbutyryl)-4-nor-3,5-seco-5-oxo-17-azaandrostan-3-oic acid 在 氨 作用下， 以 乙二醇 为溶剂， 以78%的产率得到17-(3,3-dimethylbutyryl)-4,17-diazaandrost-5-en-3-one
  参考文献：
  名称：

  Synthesis of 4,17-diazasteroid inhibitors of human 5α-reductase

  摘要：

  The synthesis of the 17-aza isomer of finasteride is described. With the side chain amide group of the compound existing in the Z configuration the structure is similar to one of the two favored conformations of finasteride. A series of 4,17-diazasteroids was assayed against the isoenzymes of human 5 alpha-reductase. Copyright (C) 1996 Elsevier Science Ltd

  DOI：

  10.1016/0968-0896(96)00109-5
• 作为产物：
  描述：

  17-(3,3-dimethylbutyryl)-17-azaandrost-4-en-3-one 在 potassium permanganate 、 sodium periodate 、 sodium carbonate 作用下， 以 叔丁醇 为溶剂， 反应 1.0h， 以71%的产率得到17-(3,3-dimethylbutyryl)-4-nor-3,5-seco-5-oxo-17-azaandrostan-3-oic acid
  参考文献：
  名称：

  Synthesis of 4,17-diazasteroid inhibitors of human 5α-reductase

  摘要：

  The synthesis of the 17-aza isomer of finasteride is described. With the side chain amide group of the compound existing in the Z configuration the structure is similar to one of the two favored conformations of finasteride. A series of 4,17-diazasteroids was assayed against the isoenzymes of human 5 alpha-reductase. Copyright (C) 1996 Elsevier Science Ltd

  DOI：

  10.1016/0968-0896(96)00109-5

文献信息

• Synthesis of 4,17-diazasteroid inhibitors of human 5α-reductase
  作者：Jacek W. Morzycki、Zenon z.xl;Lotowski、Agnieszka Z. Wilczewska、J. Darren Stuart

  DOI：10.1016/0968-0896(96)00109-5

  日期：1996.8

  The synthesis of the 17-aza isomer of finasteride is described. With the side chain amide group of the compound existing in the Z configuration the structure is similar to one of the two favored conformations of finasteride. A series of 4,17-diazasteroids was assayed against the isoenzymes of human 5 alpha-reductase. Copyright (C) 1996 Elsevier Science Ltd