A conformational restriction approach to the development of dual inhibitors of acetylcholinesterase and serotonin transporter as potential agents for Alzheimer's disease

被引:81
作者
Toda, N
Tago, K
Marumoto, S
Takami, K
Ori, M
Yamada, N
Koyama, K
Naruto, S
Abe, K
Yamazaki, R
Hara, T
Aoyagi, A
Abe, Y
Kaneko, T
Kogen, H
机构
[1] Sankyo Co Ltd, Exploratory Chem Res Labs, Shinagawa Ku, Tokyo 1408710, Japan
[2] Sankyo Co Ltd, Res Informat Dept, Shinagawa Ku, Tokyo 1408710, Japan
[3] Sankyo Co Ltd, Neurosci & Immunol Res Labs, Shinagawa Ku, Tokyo 1408710, Japan
关键词
D O I
10.1016/S0968-0896(03)00452-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alzheimer's disease (AD) has been treated with acetylcholinesterase (AChE) inhibitors such as donepezil. However, the clinical usefulness of AChE inhibitors is limited mainly due to their adverse peripheral effects. Depression seen in AD patients has been treated with serotonin transporter (SERT) inhibitors. We considered that combining SERT and AChE inhibition could improve the clinical usefulness of AChE inhibitors. In a previous paper, we found a potential dual inhibitor, 1, of AChE (IC50 = 101 nM) and SERT (IC50 = 42 nM), but its AChE inhibition activity was less than donepezil (IC50 = 10 nM). Here, we report the conformationally restricted (R)-18a considerably enhanced inhibitory activity against AChE (IC50 14 nM) and SERT (IC50 = 6 nM). (C) 2003 Elsevier Ltd. All rights reserved.
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收藏
页码:4389 / 4415
页数:27
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