Design and Synthesis of Multi-Functional Ligands through Hantzsch Reaction: Targeting Ca(2+) Channels, Activating Nrf2 and Possessing Cathepsin S Inhibitory, and Antioxidant Properties

利用Hantzsch反应设计合成多功能配体:靶向Ca²⁺通道、激活Nrf2、抑制组织蛋白酶S并具有抗氧化特性

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Abstract

This work relates to the design and synthesis of a series of novel multi-target directed ligands (MTDLs), i.e., compounds 4a-l, via a convenient one-pot three-component Hantzsch reaction. This approach targeted calcium channel antagonism, antioxidant capacity, cathepsin S inhibition, and interference with Nrf2 transcriptional activation. Of these MTDLs, 4i emerged as a promising compound, demonstrating robust antioxidant activity, the ability to activate Nrf2-ARE pathways, as well as calcium channel blockade and cathepsin S inhibition. Dihydropyridine 4i represents the first example of an MTDL that combines these biological activities.

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