4-(2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran-5-yl)-1-phenylpiperazine

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 英文名称: 4-(2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran-5-yl)-1-phenylpiperazine
• 英文别名: 1-(2,2,4,6,7-pentamethyl-3H-1-benzofuran-5-yl)-4-phenylpiperazine
• 化学式: C₂₃H₃₀N₂O
• 分子量: 350.504
• InChiKey: DQHAAPBTMCNUFJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.4
• 重原子数：
  26
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.48
• 拓扑面积：
  15.7
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  2,3,5-三甲基苯酚 在 盐酸 、 N-溴代丁二酰亚胺(NBS) 、 palladium diacetate 、 potassium carbonate 、 对甲苯磺酸 、 R-(+)-1,1'-联萘-2,2'-双二苯膦 、 N,N-二乙基苯胺 、 sodium t-butanolate 作用下， 以 水 、 乙酸乙酯 、 N,N-二甲基甲酰胺 、 甲苯 、 乙腈 为溶剂， 反应 51.75h， 生成 4-(2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran-5-yl)-1-phenylpiperazine
  参考文献：
  名称：

  Discovery of Benzofuran Derivatives that Collaborate with Insulin-Like Growth Factor 1 (IGF-1) to Promote Neuroprotection

  摘要：

  A series of benzofuran derivatives with neuroprotective activity in collaboration with IGF-1 was discovered using a newly developed cell-based assay involving primary neural cells prepared from rat hippocampal and cerebral cortical tissues. A structure activity relationship study identified compound 8 as exhibiting potent activity and brain penetrability. An in vitro pharmacological study demonstrated that although IGF-1 and 8 individually exhibited the neuroprotective effect, the latter acted in collaboration with IGF-1 to enhance neuroprotective activity.

  DOI：

  10.1021/acs.jmedchem.6b00191

文献信息

• Discovery of Benzofuran Derivatives that Collaborate with Insulin-Like Growth Factor 1 (IGF-1) to Promote Neuroprotection
  作者：Takeshi Wakabayashi、Norihito Tokunaga、Kazuyuki Tokumaru、Taiichi Ohra、Nobuyuki Koyama、Satoru Hayashi、Ryuji Yamada、Mikio Shirasaki、Yoshitaka Inui、Tetsuya Tsukamoto

  DOI：10.1021/acs.jmedchem.6b00191

  日期：2016.5.26

  A series of benzofuran derivatives with neuroprotective activity in collaboration with IGF-1 was discovered using a newly developed cell-based assay involving primary neural cells prepared from rat hippocampal and cerebral cortical tissues. A structure activity relationship study identified compound 8 as exhibiting potent activity and brain penetrability. An in vitro pharmacological study demonstrated that although IGF-1 and 8 individually exhibited the neuroprotective effect, the latter acted in collaboration with IGF-1 to enhance neuroprotective activity.