Synthesis and activity studies of N-[ω-N′-(adamant-1′-yl)aminoalkyl]-2-(4′-dimethylaminophenyl)acetamides: In the search of selective inhibitors for the different molecular forms of acetylcholinesterase
摘要:
A series of N-[omega-N'-(adamant-1'-yl)aminoalkyl]-2-(4'-dimethylaminophen were synthesized and tested as acetylcholinesterase inhibitors. A significant selectivity toward acetyl cholinesterases from various natural sources, mainly differing in their quaternary structure and solubility, was pointed out. The interest of this kind of molecules as potential therapeutic agents for Alzheimer's disease is discussed. (C) 1998 Elsevier Science Ltd. All rights reserved.
Synthesis and activity studies of N-[ω-N′-(adamant-1′-yl)aminoalkyl]-2-(4′-dimethylaminophenyl)acetamides: In the search of selective inhibitors for the different molecular forms of acetylcholinesterase
摘要:
A series of N-[omega-N'-(adamant-1'-yl)aminoalkyl]-2-(4'-dimethylaminophen were synthesized and tested as acetylcholinesterase inhibitors. A significant selectivity toward acetyl cholinesterases from various natural sources, mainly differing in their quaternary structure and solubility, was pointed out. The interest of this kind of molecules as potential therapeutic agents for Alzheimer's disease is discussed. (C) 1998 Elsevier Science Ltd. All rights reserved.
Synthesis and activity studies of N-[ω-N′-(adamant-1′-yl)aminoalkyl]-2-(4′-dimethylaminophenyl)acetamides: In the search of selective inhibitors for the different molecular forms of acetylcholinesterase
作者:Emanuele Perola、Luciano Cellai、Mario Brufani
DOI:10.1016/s0960-894x(98)00076-6
日期:1998.3
A series of N-[omega-N'-(adamant-1'-yl)aminoalkyl]-2-(4'-dimethylaminophen were synthesized and tested as acetylcholinesterase inhibitors. A significant selectivity toward acetyl cholinesterases from various natural sources, mainly differing in their quaternary structure and solubility, was pointed out. The interest of this kind of molecules as potential therapeutic agents for Alzheimer's disease is discussed. (C) 1998 Elsevier Science Ltd. All rights reserved.