Acta Pharmaceutica Sinica B
|
2025, 15(8): 4156-4173
• Original articles •
A novel C-3-substituted oleanolic acid benzyl amide derivative exhibits therapeutic potential against influenza A by targeting PA-PB1 interactions and modulating host macrophage inflammation
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Kunyu Lu1, Jianfu He1, Chongjun Hong2, Haowei Li1, Jiaai Ruan2, Jinshen Wang1, Haoxing Yuan1, Binhao Rong1, Chan Yang3,4, Gaopeng Song2, Shuwen Liu1,5,3,4
Affiliations
1 Guangdong Provincial Key Laboratory of New Drug Screening, NMPA Key Laboratory of Drug Metabolism Research and Evaluation, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515, China;
2 Key Laboratory for Biobased Materials and Energy of Ministry of Education, College of Materials and Energy, South China Agricultural University, Guangzhou 510642, China;
3 The Tenth Affiliated Hospital of Southern Medical University (Dongguan People's Hospital), Southern Medical University, Dongguan 523018, China;
4 MOE Key Laboratory of Infectious Diseases Research in South China, Southern Medical University, Guangzhou 510515, China;
5 State Key Laboratory of Organ Failure Research, Guangdong Provincial Institute of Nephrology, Southern Medical University, Guangzhou 510515, China
doi: 10.1016/j.apsb.2025.05.031
Outline
The influenza A virus (IAV), renowned for its high contagiousness and potential to catalyze global pandemics, poses significant challenges due to the emergence of drug-resistant strains. Given the critical role of RNA polymerase in IAV replication, it stands out as a promising target for anti-IAV therapies. In this study, we identified a novel C-3-substituted oleanolic acid benzyl amide derivative, A5, as a potent inhibitor of the PAC-PB1N polymerase subunit interaction, with an IC₅₀ value of 0.96 ± 0.21 μmol/L. A5 specifically targets the highly conserved PAC domain and demonstrates remarkable efficacy against both laboratory-adapted and clinically isolated IAV strains, including multidrug-resistant strains, with EC₅₀ values ranging from 0.60 to 1.83 μmol/L. Notably, when combined with oseltamivir, A5 exhibits synergistic effects both in vitro and in vivo. In a murine model, dose-dependent administration of A5 leads to a significant reduction in IAV titers, resulting in a high survival rate among treated mice. Additionally, A5 treatment inhibits virus-induced Toll-like receptor 4 activation, attenuates cytokine responses, and protects against IAV-induced inflammatory responses in macrophages. In summary, A5 emerges as a novel inhibitor with high efficiency and broad-spectrum anti-influenza activity.
Influenza A virus
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RNA polymerase
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Protein-protein interaction
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Pentacyclic triterpenoids
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Oleanolic acid amide derivatives
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Drug-resistant strains
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Inflammation
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Toll-like receptor 4
Kunyu Lu, Jianfu He, Chongjun Hong, Haowei Li, Jiaai Ruan, Jinshen Wang, Haoxing Yuan, Binhao Rong, Chan Yang, Gaopeng Song, Shuwen Liu.
A novel C-3-substituted oleanolic acid benzyl amide derivative exhibits therapeutic potential against influenza A by targeting PA-PB1 interactions and modulating host macrophage inflammation[J].
Acta Pharmaceutica Sinica B,
2025
, 15
(8)
: 4156
-4173
.
DOI: 10.1016/j.apsb.2025.05.031
Year 2025 volume 15 Issue 8
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Article Info
doi: 10.1016/j.apsb.2025.05.031
- Receive Date:2024-10-20
- Online Date:2026-09-17