1,1,5,5-tetramethyloctahydro-2,4α-methanonaphthalen-7-one

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: 1,1,5,5-tetramethyloctahydro-2,4α-methanonaphthalen-7-one
• 英文别名: (3S,6S,9R)-2,2,8,8-tetramethyl-octahydro-1H-2,4a-methanonapthalenone
• 化学式: C₁₅H₂₄O
• 分子量: 220.355
• InChiKey: MWPBNGVYOHBVGM-NVBFEUDRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  16
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.93
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  4,4'-二羟基二苯甲酮 、 1,1,5,5-tetramethyloctahydro-2,4α-methanonaphthalen-7-one 在 四氯化钛 、 锌 作用下， 以 四氢呋喃 为溶剂， 反应 1.5h， 以67%的产率得到7-[bis(4-hydroxyphenyl)methylene]-1,1,5,5-tetramethyloctahydro-2,4α-methanonaphthalene
  参考文献：
  名称：

  Bridged Bicyclic Cores Containing a 1,1-Diarylethylene Motif Are High-Affinity Subtype-Selective Ligands for the Estrogen Receptor

  摘要：

  The actions of estrogens are mediated through the two estrogen receptors, ERalpha and ERbeta. Compounds that interact selectively with ERalpha or ERbeta are of interest because they could be used to explore the biological roles of these ER subtypes and they might be interesting estrogen pharmaceuticals. In a new approach to develop ER subtype-selective ligands, we have embellished the 1,1-diarylethylene motif, common to many nonsteroidal estrogens, with various bridged bicyclic or tricyclic cores, including ones based on bicyclo [3.3.1] nonane, bicyclo [2.2.1] heptane, and selected bi- and tricyclic terpenoids. This design leads to three-dimensional ER ligands of unusual structure that we have used to probe the size and shape of the ligand binding pocket of ERalpha and ERbeta. Many of these compounds have high binding affinities, with the best having a bicyclo[3.3.1]nonane core and binding 3-5 times better than estradiol to both ER subtypes. Some of the compounds show significant affinity selectivity in favor of ERbeta (4- to 5-fold), and in cell-based assays for transcriptional activity most are partial agonists on ERalpha and full antagonists on ERbeta.

  DOI：

  10.1021/jm0204800
• 作为产物：
  描述：

  (-)-异长叶烯-9-酮 在 氨 、 lithium 作用下， 以 四氢呋喃 为溶剂， 反应 0.17h， 以82%的产率得到1,1,5,5-tetramethyloctahydro-2,4α-methanonaphthalen-7-one
  参考文献：
  名称：

  Bridged Bicyclic Cores Containing a 1,1-Diarylethylene Motif Are High-Affinity Subtype-Selective Ligands for the Estrogen Receptor

  摘要：

  The actions of estrogens are mediated through the two estrogen receptors, ERalpha and ERbeta. Compounds that interact selectively with ERalpha or ERbeta are of interest because they could be used to explore the biological roles of these ER subtypes and they might be interesting estrogen pharmaceuticals. In a new approach to develop ER subtype-selective ligands, we have embellished the 1,1-diarylethylene motif, common to many nonsteroidal estrogens, with various bridged bicyclic or tricyclic cores, including ones based on bicyclo [3.3.1] nonane, bicyclo [2.2.1] heptane, and selected bi- and tricyclic terpenoids. This design leads to three-dimensional ER ligands of unusual structure that we have used to probe the size and shape of the ligand binding pocket of ERalpha and ERbeta. Many of these compounds have high binding affinities, with the best having a bicyclo[3.3.1]nonane core and binding 3-5 times better than estradiol to both ER subtypes. Some of the compounds show significant affinity selectivity in favor of ERbeta (4- to 5-fold), and in cell-based assays for transcriptional activity most are partial agonists on ERalpha and full antagonists on ERbeta.

  DOI：

  10.1021/jm0204800

文献信息

• Bridged Bicyclic Cores Containing a 1,1-Diarylethylene Motif Are High-Affinity Subtype-Selective Ligands for the Estrogen Receptor
  作者：Rajeev S. Muthyala、Shubin Sheng、Kathryn E. Carlson、Benita S. Katzenellenbogen、John. A. Katzenellenbogen

  DOI：10.1021/jm0204800

  日期：2003.4.1

  The actions of estrogens are mediated through the two estrogen receptors, ERalpha and ERbeta. Compounds that interact selectively with ERalpha or ERbeta are of interest because they could be used to explore the biological roles of these ER subtypes and they might be interesting estrogen pharmaceuticals. In a new approach to develop ER subtype-selective ligands, we have embellished the 1,1-diarylethylene motif, common to many nonsteroidal estrogens, with various bridged bicyclic or tricyclic cores, including ones based on bicyclo [3.3.1] nonane, bicyclo [2.2.1] heptane, and selected bi- and tricyclic terpenoids. This design leads to three-dimensional ER ligands of unusual structure that we have used to probe the size and shape of the ligand binding pocket of ERalpha and ERbeta. Many of these compounds have high binding affinities, with the best having a bicyclo[3.3.1]nonane core and binding 3-5 times better than estradiol to both ER subtypes. Some of the compounds show significant affinity selectivity in favor of ERbeta (4- to 5-fold), and in cell-based assays for transcriptional activity most are partial agonists on ERalpha and full antagonists on ERbeta.