Design, synthesis, and biological evaluation of 2-arylethenylquinoline derivatives as multifunctional agents for the treatment of Alzheimer's disease.

Abstract

A series of new 2-arylethenylquinoline derivatives (4a1-4a12, 4b1-4b8, 4c1-4c4, 4d1-4d3 and 4e1-4e9) were designed, synthesized, and evaluated as potential multifunctional agents for the treatment of Alzheimer's disease (AD). In vitro studies showed that these synthetic compounds inhibited self-induced Aβ1-42 aggregation effectively ranged from 23.6% to 83.9% at the concentration of 20 μM, and acted as potential antioxidants and biometal chelators. Their structure-activity relationships were obtained and discussed. In particular, compound 4b1, the most active compound, displayed strong inhibitory activity with an IC50 value of 9.7 μM for self-induced Aβ1-42 aggregation, good antioxidative activity with a value of 3.9-fold of Trolox, potent inhibitory activity for cholinesterase with IC50 values of 0.2 μM and 64.1 μM against butyrylcholinesterase (BuChE) and acetylcholinesterase (AChE), respectively. Besides, 4b1 was also capable of disassembling the self-induced Aβ1-42 aggregation fibrils with a ratio of 59.8% at 20 μM concentration, and had a good metal chelating activity. Taken together, these results suggest that compound 4b1 might be a promising lead compound for AD treatment.

• Authors: Xiao-Qin Wang, Chun-Li Xia, Shuo-Bin Chen, Jia-Heng Tan, Tian-Miao Ou, Shi-Liang Huang, Ding Li, Lian-Quan Gu, Zhi-Shu Huang
• Journal: European journal of medicinal chemistry (Eur J Med Chem) Vol. 89 Pg. 349-61 (Jan 07 2015) ISSN: 1768-3254 [Electronic] France
• PMID: 25462251 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2014 Elsevier Masson SAS. All rights reserved.

Chemical References

• Amyloid beta-Peptides
• Antioxidants
• Chelating Agents
• Cholinesterase Inhibitors
• Peptide Fragments
• Quinolines
• Stilbenes
• amyloid beta-protein (1-42)

Topics

• Alzheimer Disease (drug therapy, enzymology, metabolism)
• Amyloid beta-Peptides (metabolism)
• Antioxidants (chemical synthesis, chemistry, pharmacology)
• Cell Line, Tumor
• Cell Survival (drug effects)
• Chelating Agents (chemical synthesis, chemistry, pharmacology)
• Cholinesterase Inhibitors (chemical synthesis, chemistry, pharmacology)
• Drug Design
• Humans
• Molecular Structure
• Peptide Fragments (metabolism)
• Quinolines (chemical synthesis, chemistry, pharmacology)
• Stilbenes (chemical synthesis, chemistry, pharmacology)