(1R,3aR,7aR)-7a-Methyl-1-((R)-1,4,4,6,6-pentamethyl-5-oxo-heptyl)-octahydro-inden-4-one | 866759-11-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (1R,3aR,7aR)-7a-Methyl-1-((R)-1,4,4,6,6-pentamethyl-5-oxo-heptyl)-octahydro-inden-4-one
• CAS: 866759-11-7
• 化学式: C₂₂H₃₈O₂
• 分子量: 334.543
• InChiKey: LIEFRICREQIEMR-DBHNTLKXSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.83
• 重原子数：
  24.0
• 可旋转键数：
  5.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.91
• 拓扑面积：
  34.14
• 氢给体数：
  0.0
• 氢受体数：
  2.0

反应信息

• 作为反应物：
  描述：

  (1R,3aR,7aR)-7a-Methyl-1-((R)-1,4,4,6,6-pentamethyl-5-oxo-heptyl)-octahydro-inden-4-one 在 正丁基锂 、 四丁基氟化铵 作用下， 以 四氢呋喃 、 正己烷 为溶剂， 反应 5.0h， 生成 (R)-7-{(1R,3aS,7aR)-4-[2-[(3S,5R)-3,5-Dihydroxy-2-methylene-cyclohex-(Z)-ylidene]-eth-(E)-ylidene]-7a-methyl-octahydro-inden-1-yl}-2,2,4,4-tetramethyl-octan-3-one
  参考文献：
  名称：

  Highly antiproliferative, low-calcemic, side-chain ketone analogs of the hormone 1α,25-dihydroxyvitamin D3

  摘要：

  A series 2a-4b of seven new side-chain ketone analogs of calcitriol (1) have been prepared. Unexpectedly, several of these 24- and 25-tert-butyl ketones, even though lacking the classical side-chain tertiary hydroxyl group, are considerably more antiproliferative in vitro than the hormone calcitriol (1) even at physiologically relevant low nanomolar concentrations and are less calcemic than calcitriol (1) in vivo. In addition, ketone analog 19-nor-2a is not significantly less calcemic in vivo than 19-methylene analog 2a. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2005.06.031
• 作为产物：
  描述：

  (R)-7-((1R,3aR,4S,7aR)-4-Hydroxy-7a-methyl-octahydro-inden-1-yl)-2,2,4,4-tetramethyl-octan-3-one 在 重铬酸吡啶 、 Celite 作用下， 以 二氯甲烷 为溶剂， 以94%的产率得到(1R,3aR,7aR)-7a-Methyl-1-((R)-1,4,4,6,6-pentamethyl-5-oxo-heptyl)-octahydro-inden-4-one
  参考文献：
  名称：

  Highly antiproliferative, low-calcemic, side-chain ketone analogs of the hormone 1α,25-dihydroxyvitamin D3

  摘要：

  A series 2a-4b of seven new side-chain ketone analogs of calcitriol (1) have been prepared. Unexpectedly, several of these 24- and 25-tert-butyl ketones, even though lacking the classical side-chain tertiary hydroxyl group, are considerably more antiproliferative in vitro than the hormone calcitriol (1) even at physiologically relevant low nanomolar concentrations and are less calcemic than calcitriol (1) in vivo. In addition, ketone analog 19-nor-2a is not significantly less calcemic in vivo than 19-methylene analog 2a. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2005.06.031

文献信息

• WO2006/74227
  申请人：——

  公开号：——

  公开（公告）日：——