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.

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Journal
Viruses
Published
2025-12-24
DOI
https://doi.org/10.3390/v18010033
Primary Topic
HIV/AIDS drug development and treatment
Type
article
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article

Anti-HIV-1 Activity of the Integrase Strand Transfer Inhibitor ACC017

Heliang Fu, Yong‐Tang Zheng, Guan-Cheng Huang, Rong-Hua Luo et al.
Viruses
HIV/AIDS drug development and treatment
article

Anti-HIV-1 Activity of the Integrase Strand Transfer Inhibitor ACC017

Heliang Fu, Yong‐Tang Zheng, Guan-Cheng Huang, Rong-Hua Luo, Xin-Yan Long, Chun-Yan Li, Feng-Ying He, Meng-Di Ma, Liu-Meng Yang
article en

Abstract

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.

VirusesVol. 18(1)
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)
Good health and well-being
Openalex Percentile: Top 31%
HIV/AIDS drug development and treatment
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Anti-HIV-1 Activity of the Integrase Strand Transfer Inhibitor ACC017 — Heliang Fu, Yong‐Tang Zheng, et al. · Viruses (2025) | TGRS Research Map | TGRS