| Literature DB >> 29500132 |
Rui Xu1, Ganyuan Xiao1, Yan Li1, Hongyan Liu1, Qing Song1, Xiaoyu Zhang1, Ziyi Yang1, Yunxiaozhu Zheng1, Zhenghuai Tan2, Yong Deng3.
Abstract
A series of 5,6-dimethoxybenzo[d]isothiazol-3(2H)-one-N-alkylbenzylamine derivatives were designed, synthesized and evaluated as potential multifunctional agents for the treatment of Alzheimer's disease (AD). The in vitro assays indicated that most of these derivatives were selective AChE inhibitors with good multifunctional properties. Among them, compounds 11b and 11d displayed comprehensive advantages, with good AChE (IC50 = 0.29 ± 0.01 μM and 0.46 ± 0.02 μM, respectively), MAO-A (IC50 = 8.2 ± 0.08 μM and 7.9 ± 0.07 μM, respectively) and MAO-B (IC50 = 20.1 ± 0.16 μM and 43.8 ± 2.0% at 10 μM, respectively) inhibitory activities, moderate self-induced Aβ1-42 aggregation inhibitory potency (35.4 ± 0.42% and 48.0 ± 1.53% at 25 μM, respectively) and potential antioxidant activity. In addition, the two representative compounds displayed high BBB permeability in vitro. Taken together, these multifunctional properties make 11b and 11d as a promising candidate for the development of efficient drugs against AD.Entities:
Keywords: Acetylcholinesterase inhibitors; Alzheimer’s disease; Aβ aggregation inhibitors; Benzo[d]isothiazol-3(2H)-one derivatives; Monoamine oxidase inhibitors; Multifunctional agents
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Year: 2018 PMID: 29500132 DOI: 10.1016/j.bmc.2018.02.037
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641