کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1394242 | 1501140 | 2014 | 18 صفحه PDF | دانلود رایگان |

• Genistein derivatives with carbon spacer-linked alkylbenzylamines were synthesized.
• Most compounds exhibited good acetylcholinesterase inhibitory and antioxidant activity.
• Some compounds exhibited potent inhibition Aβ aggregation.
• Some compounds markedly disassembled the Cu2+-induced Aβ aggregation.
• Some compounds significantly reversed scopolamine-induced memory deficit in mice.
A series of genistein derivatives with carbon spacer-linked alkylbenzylamines were designed, synthesized and tested as multifunctional agents for the treatment of Alzheimer's disease (AD). The results showed that most of these compounds exhibited good acetylcholinesterase (AChE) inhibitory activity, with moderate-to-good anti-oxidative activity. Specifically, compounds 10b, 19d and 25d exhibited significant inhibition of β-amyloid (Aβ) aggregation and exhibited metal chelating properties. In particular, 25d inhibited: self-induced Aβ1–42 aggregation, Cu2+-induced Aβ1–42 aggregation, and human AChE-induced Aβ1–40 aggregation by 35%, 77.8%, and 36.2%, respectively. Moreover, both kinetic analysis of AChE inhibition and the molecular modeling study suggested that 25d binds simultaneously to catalytic active site and peripheral anionic site of AChE. More importantly, compound 25d disassembled the well-structured Aβ fibrils generated by Cu2+-induced Aβ aggregation by 72.1%. Furthermore, the step-down passive avoidance test showed this compound significantly reversed scopolamine-induced memory deficit in mice. These results suggest that 25d may be a promising multifunctional agent for AD treatment.
A series of genistein derivatives with carbon spacer-linked alkylbenzylamines were designed, synthesized and tested as multifunctional agents for the treatment of Alzheimer's disease (AD). Compound 25d may be a promising multifunctional agent for AD treatment. Figure optionsDownload as PowerPoint slide
Journal: European Journal of Medicinal Chemistry - Volume 76, 9 April 2014, Pages 314–331