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Novel Acyl Thiourea-Based Hydrophobic Tagging Degraders Exert Potent Anti-Influenza Activity through Two Distinct Endonuclease Polymerase Acidic-Targeted Degradation Pathways

Xiaoyu Ma, Xueyun Wang, Feifei Chen, Wenting Zou, Junrui Ren, Lilan Xin, Pei He, Jinsen Liang, Zhichao Xu, Chune Dong, Ke Lan, Shuwen Wu, Hai‐Bing Zhou

2024Journal of Medicinal Chemistry20 citationsDOI

Abstract

The spread of the influenza virus has caused devastating pandemics and huge economic losses worldwide. Antiviral drugs with diverse action modes are urgently required to overcome the challenges of viral mutation and drug resistance, and targeted protein degradation strategies constitute excellent candidates for this purpose. Herein, the first degradation of the influenza virus polymerase acidic (PA) protein using small-molecule degraders developed by hydrophobic tagging (HyT) technology to effectively combat the influenza virus was reported. The SAR results revealed that compound 19b with Boc 2 –( L )-Lys demonstrated excellent inhibitory activity against A/WSN/33/H1N1 (EC 50 = 0.015 μM) and amantadine-resistant strain (A/PR/8/H1N1), low cytotoxicity, high selectivity, substantial degradation ability, and good drug-like properties. Mechanistic studies demonstrated that the proteasome system and autophagic lysosome pathway were the potential drivers of these HyT degraders. Thus, this study provides a powerful tool for investigating the targeted degradation of influenza virus proteins and for antiviral drug development.

Topics & Concepts

ChemistryInfluenza A virusVirusCytotoxicityProtein degradationViral proteinVirologyBiochemistryMicrobiologyIn vitroBiologyProtein Degradation and InhibitorsUbiquitin and proteasome pathwaysHIV Research and Treatment