(1-Benzyl-piperidin-4-ylmethyl)-(2,6-dimethoxy-5-methyl-5,6,7,8-tetrahydro-quinolin-5-yl)-amine | 259653-68-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: (1-Benzyl-piperidin-4-ylmethyl)-(2,6-dimethoxy-5-methyl-5,6,7,8-tetrahydro-quinolin-5-yl)-amine
• 英文别名: N-[(1-benzylpiperidin-4-yl)methyl]-2,6-dimethoxy-5-methyl-7,8-dihydro-6H-quinolin-5-amine
• CAS: 259653-68-4
• 化学式: C₂₅H₃₅N₃O₂
• 分子量: 409.572
• InChiKey: GEAUSXVZTKJMQR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  30
• 可旋转键数：
  7
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.56
• 拓扑面积：
  46.6
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  (1-Benzyl-piperidin-4-ylmethyl)-(2,6-dimethoxy-5-methyl-5,6,7,8-tetrahydro-quinolin-5-yl)-amine 在 碘代三甲硅烷 作用下， 以 氯仿 为溶剂， 以58%的产率得到5-[(1-Benzyl-piperidin-4-ylmethyl)-amino]-6-hydroxy-5-methyl-5,6,7,8-tetrahydro-1H-quinolin-2-one
  参考文献：
  名称：

  Synthesis and acetylcholinesterase inhibitory activity of huperzine A—E2020 combined compound

  摘要：

  The synthesis of huperzine-E2020 combined compound (3) has been accomplished and the activities of 3 and the intermediates 12 and 13 to inhibit the activity of acetylcholinesterase have been measured. Conformation analyses and molecular docking studies of E2020 and the eight isomers of 12 were carried out. The results indicated that binding energies of all isomers of 12 with AChE was much lowe; than E2020 except for isomer RRZ, which might be the reason that the activity of 12 was lower than that of E2020. Interaction pattern of RRZ in AChE was also studied. Both binding energy and interaction pattern shows that the biological activity of RRZ might be higher than that of E2020. (C) 1999 Elsevier Science Ltd. Ail rights reserved.

  DOI：

  10.1016/s0960-894x(99)00597-1
• 作为产物：
  描述：

  (2,6-Dimethoxy-5-methyl-5,6,7,8-tetrahydro-quinolin-5-yl)-carbamic acid methyl ester 在 氢氧化钾 、 lithium aluminium tetrahydride 、 18-冠醚-6 、 N,N'-二环己基碳二亚胺 作用下， 以 乙醚 、 二氯甲烷 、 甲苯 为溶剂， 生成 (1-Benzyl-piperidin-4-ylmethyl)-(2,6-dimethoxy-5-methyl-5,6,7,8-tetrahydro-quinolin-5-yl)-amine
  参考文献：
  名称：

  Synthesis and acetylcholinesterase inhibitory activity of huperzine A—E2020 combined compound

  摘要：

  The synthesis of huperzine-E2020 combined compound (3) has been accomplished and the activities of 3 and the intermediates 12 and 13 to inhibit the activity of acetylcholinesterase have been measured. Conformation analyses and molecular docking studies of E2020 and the eight isomers of 12 were carried out. The results indicated that binding energies of all isomers of 12 with AChE was much lowe; than E2020 except for isomer RRZ, which might be the reason that the activity of 12 was lower than that of E2020. Interaction pattern of RRZ in AChE was also studied. Both binding energy and interaction pattern shows that the biological activity of RRZ might be higher than that of E2020. (C) 1999 Elsevier Science Ltd. Ail rights reserved.

  DOI：

  10.1016/s0960-894x(99)00597-1

文献信息

• Synthesis and acetylcholinesterase inhibitory activity of huperzine A—E2020 combined compound
  作者：Fanxing Zeng、Hualiang Jiang、Yufeng Zhai、Haiyan Zhang、Kaixian Chen、Ruyun Ji

  DOI：10.1016/s0960-894x(99)00597-1

  日期：1999.12

  The synthesis of huperzine-E2020 combined compound (3) has been accomplished and the activities of 3 and the intermediates 12 and 13 to inhibit the activity of acetylcholinesterase have been measured. Conformation analyses and molecular docking studies of E2020 and the eight isomers of 12 were carried out. The results indicated that binding energies of all isomers of 12 with AChE was much lowe; than E2020 except for isomer RRZ, which might be the reason that the activity of 12 was lower than that of E2020. Interaction pattern of RRZ in AChE was also studied. Both binding energy and interaction pattern shows that the biological activity of RRZ might be higher than that of E2020. (C) 1999 Elsevier Science Ltd. Ail rights reserved.