1-((1S,4aS,8aS)-2,5,5,8a-Tetramethyl-1,4,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl)-pent-4-en-2-ol | 195702-77-3

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-((1S,4aS,8aS)-2,5,5,8a-Tetramethyl-1,4,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl)-pent-4-en-2-ol
• 英文别名: 1-[(1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]pent-4-en-2-ol
• CAS: 195702-77-3
• 化学式: C₁₉H₃₂O
• 分子量: 276.462
• InChiKey: UUURDKSGECDKAX-OSCZMGMTSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.4
• 重原子数：
  20
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.79
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  1-((1S,4aS,8aS)-2,5,5,8a-Tetramethyl-1,4,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl)-pent-4-en-2-ol 在 pyridine-SO3 complex 作用下， 反应 24.0h， 生成 1-[(1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]pent-4-en-2-yl hydrogen sulfate
  参考文献：
  名称：

  Synthesis and phosphatase inhibitory activity of analogs of sulfircin

  摘要：

  Analogs of sulfircin (1) were synthesized and tested for inhibitory activity against a panel of phosphatases. We attempted to optimize the potency and selectivity of sulfircin for Cdc25A by modifying three structural areas of the molecule. An anionic group is required for potency and malonate was found to be an effective substitute for sulfate. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0960-894x(97)00357-0
• 作为产物：
  描述：

  methyl 2-((1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,5,6,7,8,8a-octahydronaphthalen-1-yl)acetate 在 lithium aluminium tetrahydride 、 草酰氯 、 二甲基亚砜 、 三乙胺 作用下， 以 四氢呋喃 、 乙醚 、 二氯甲烷 为溶剂， 反应 2.25h， 生成 1-((1S,4aS,8aS)-2,5,5,8a-Tetramethyl-1,4,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl)-pent-4-en-2-ol
  参考文献：
  名称：

  Synthesis and phosphatase inhibitory activity of analogs of sulfircin

  摘要：

  Analogs of sulfircin (1) were synthesized and tested for inhibitory activity against a panel of phosphatases. We attempted to optimize the potency and selectivity of sulfircin for Cdc25A by modifying three structural areas of the molecule. An anionic group is required for potency and malonate was found to be an effective substitute for sulfate. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0960-894x(97)00357-0

文献信息

• Synthesis and phosphatase inhibitory activity of analogs of sulfircin
  作者：Regina E. Cebula、Jill L. Blanchard、Michael D. Boisclair、Kollol Pal、Nicholas J. Bockovich

  DOI：10.1016/s0960-894x(97)00357-0

  日期：1997.8

  Analogs of sulfircin (1) were synthesized and tested for inhibitory activity against a panel of phosphatases. We attempted to optimize the potency and selectivity of sulfircin for Cdc25A by modifying three structural areas of the molecule. An anionic group is required for potency and malonate was found to be an effective substitute for sulfate. (C) 1997 Elsevier Science Ltd.