Anti-HIV-1 Activity of the Integrase Strand Transfer Inhibitor ACC017
HIV-1 integrase strand transfer inhibitors (INSTIs) are pivotal to antiretroviral therapy. However, the emergence of drug-resistant mutations necessitates the development of new agents. Here, we present ACC017 as a novel INSTI candidate. ACC017 demonstrated potent activity against the laboratory-adapted HIV-1<sub>IIIB</sub> strain (EC<sub>50</sub> = 0.59 nM; SI > 34,525) and maintained efficacy against a panel of drug-resistant strains (EC<sub>50</sub> range from 0.34 to 9.12 nM) and clinical isolated strains (EC<sub>50</sub> range from 0.11 to 1.78 nM). Mechanism of action studies confirmed its ability to inhibit the integrase enzyme (IC<sub>50</sub> = 9.19 nM) and effectively block viral genome integration. Notably, in vitro resistance selection primarily yielded D232N and R263K mutations, without the emergence of G140S/A/C/R or Q148H/R/K. This promising profile, combined with synergistic interactions with other antiretroviral drugs, positions ACC017 as a potential therapeutic option.
Authors
- Heliang Fu
- Yong‐Tang Zheng (ORCID: https://orcid.org/0000-0001-5469-0324)
- Guan-Cheng Huang
- Rong-Hua Luo
- Xin-Yan Long
- Chun-Yan Li
- Feng-Ying He
- Meng-Di Ma
- Liu-Meng Yang
Institutions
- Kunming Institute of Zoology (CN)
- Chengdu Organic Chemicals (China) (CN)
- Yangtze River Pharmaceutical Group (China) (CN)
- University of Chinese Academy of Sciences (CN)
- Dali University (CN)
- University of Hong Kong (HK)
Publication Details
- Journal
- Viruses
- Published
- 2025-12-24
- DOI
- https://doi.org/10.3390/v18010033
- Primary Topic
- HIV/AIDS drug development and treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00