(1R,3aS,5S,7aR)-5-cyclohexyl-α,3a-oxide-7a-methylperhydroindene-1-ethanol | 392235-24-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 氧杂环己烷
• 英文名称: (1R,3aS,5S,7aR)-5-cyclohexyl-α,3a-oxide-7a-methylperhydroindene-1-ethanol
• 英文别名: (1S,3S,6R,7R)-3-cyclohexyl-6-methyl-10-oxatricyclo[5.3.2.01,6]dodecan-9-ol
• CAS: 392235-24-4
• 化学式: C₁₈H₃₀O₂
• 分子量: 278.435
• InChiKey: PKCYPBWRLHHNMH-MJWQQNNUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5
• 重原子数：
  20
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  29.5
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-(氨基氧基)乙胺 、 (1R,3aS,5S,7aR)-5-cyclohexyl-α,3a-oxide-7a-methylperhydroindene-1-ethanol 在 盐酸 作用下， 以 1,4-二氧六环 为溶剂， 反应 16.0h， 生成 (1R,3aS,5S,7aR)-1-[(2Z)-2-(2-aminoethoxyimino)ethyl]-5-cyclohexyl-7a-methyl-2,3,4,5,6,7-hexahydro-1H-inden-3a-ol 、 (1R,3aS,5S,7aR)-1-[2-aminoethoxy-(E)-iminoethyl]-5-cyclohexyl-7a-methylperhydroinden-3a-ol
  参考文献：
  名称：

  Synthesis and Inotropic Activity of 1-(O-Aminoalkyloximes) of Perhydroindene Derivatives as Simplified Digitalis-like Compounds Acting on the Na⁺,K⁺-ATPase

  摘要：

  A series of 5-substituted (3aS,7aR)-7a-methylperhydroinden-3a-ol derivatives bearing a 1(S)(omega-aminoalkoxy)iminoalkyl or -alkenyl substituent was synthesized, starting from the Hajos-Parrish ketol 47, as simplified analogues of very potent 17beta-aminoalkyloximes with digitalis skeleton, previously reported. The target compounds were evaluated in vitro for displacement of the specific [H-3]ouabain binding from the dog kidney Na+,K+-ATPase receptor. Some of them revealed IC50 values in the micromolar range. The most active compounds possess a cyclohexyl group in the 5(S) position and in position 1(S) the same aminoalkyloxime groups already reported for the digitoxigenin-like series in position 17beta. Although the ring conformation of these derivatives was comparable to that of uzarigenin, the binding affinities of the most active ones were 4/8-fold lower in comparison to that standard, Three compounds among those with the highest affinities were assayed in vitro for their inotropic activity on an electrically driven guinea pig left atrium and were found to be less potent than both digoxin, the most widely used inotropic agent, and the corresponding digitalis 17beta-aminoalkyloximes.

  DOI：

  10.1021/jm011001k
• 作为产物：
  描述：

  (+)-六氢-3a-羟基-7a-甲基-1H-茚-1,5(6H)-二酮 在 5percent Rh/Al₂₀₃ 硼烷 、 potassium tert-butylate 、 氢气 、 草酸 、 镍 、 对甲苯磺酸 、 2-碘酰基苯甲酸 作用下， 以 四氢呋喃 、 甲醇 、 乙醚 、 乙醇 、 环己烷 、 水 、 二甲基亚砜 、 乙腈 、 叔丁醇 为溶剂， -78.0~20.0 ℃ 、435.73 kPa 条件下， 反应 79.17h， 生成 (1R,3aS,5S,7aR)-5-cyclohexyl-α,3a-oxide-7a-methylperhydroindene-1-ethanol
  参考文献：
  名称：

  Synthesis and Inotropic Activity of 1-(O-Aminoalkyloximes) of Perhydroindene Derivatives as Simplified Digitalis-like Compounds Acting on the Na⁺,K⁺-ATPase

  摘要：

  A series of 5-substituted (3aS,7aR)-7a-methylperhydroinden-3a-ol derivatives bearing a 1(S)(omega-aminoalkoxy)iminoalkyl or -alkenyl substituent was synthesized, starting from the Hajos-Parrish ketol 47, as simplified analogues of very potent 17beta-aminoalkyloximes with digitalis skeleton, previously reported. The target compounds were evaluated in vitro for displacement of the specific [H-3]ouabain binding from the dog kidney Na+,K+-ATPase receptor. Some of them revealed IC50 values in the micromolar range. The most active compounds possess a cyclohexyl group in the 5(S) position and in position 1(S) the same aminoalkyloxime groups already reported for the digitoxigenin-like series in position 17beta. Although the ring conformation of these derivatives was comparable to that of uzarigenin, the binding affinities of the most active ones were 4/8-fold lower in comparison to that standard, Three compounds among those with the highest affinities were assayed in vitro for their inotropic activity on an electrically driven guinea pig left atrium and were found to be less potent than both digoxin, the most widely used inotropic agent, and the corresponding digitalis 17beta-aminoalkyloximes.

  DOI：

  10.1021/jm011001k

文献信息

• Synthesis and Inotropic Activity of 1-(<i>O</i>-Aminoalkyloximes) of Perhydroindene Derivatives as Simplified Digitalis-like Compounds Acting on the Na⁺,K⁺-ATPase
  作者：Alberto Cerri、Nicoletta Almirante、Paolo Barassi、Alessandra Benicchio、Sergio De Munari、Giuseppe Marazzi、Isabella Molinari、Fulvio Serra、Piero Melloni

  DOI：10.1021/jm011001k

  日期：2002.1.1

  A series of 5-substituted (3aS,7aR)-7a-methylperhydroinden-3a-ol derivatives bearing a 1(S)(omega-aminoalkoxy)iminoalkyl or -alkenyl substituent was synthesized, starting from the Hajos-Parrish ketol 47, as simplified analogues of very potent 17beta-aminoalkyloximes with digitalis skeleton, previously reported. The target compounds were evaluated in vitro for displacement of the specific [H-3]ouabain binding from the dog kidney Na+,K+-ATPase receptor. Some of them revealed IC50 values in the micromolar range. The most active compounds possess a cyclohexyl group in the 5(S) position and in position 1(S) the same aminoalkyloxime groups already reported for the digitoxigenin-like series in position 17beta. Although the ring conformation of these derivatives was comparable to that of uzarigenin, the binding affinities of the most active ones were 4/8-fold lower in comparison to that standard, Three compounds among those with the highest affinities were assayed in vitro for their inotropic activity on an electrically driven guinea pig left atrium and were found to be less potent than both digoxin, the most widely used inotropic agent, and the corresponding digitalis 17beta-aminoalkyloximes.