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Identification of a Non-Nucleoside Reverse Transcriptase Inhibitor against Human Immunodeficiency Virus-1

  • Min Jung Kim
  • , Kyung Lee Yu
  • , Ri Han
  • , Yoonji Lee
  • , Kyungsoo Oh
  • , Ji Chang You
  • Avixgen Inc.
  • The Catholic University of Korea, College of Medicine
  • Chung-Ang University

Research output: Contribution to journal › Article › peer-review

7 Scopus citations

Abstract

The HIV-1 infection epidemic remains a global health problem. Current antiretroviral treatments are effective in controlling the progression of a severe infection. However, the emergence of drug resistance requires an urgent identification of new treatment regimes. HIV-1 reverse transcriptase (RTs) has been a successful therapeutic target owing to its high specificity and potent antiviral properties; therefore, it has become an essential component of current HIV-1 standard treatments. This study identified a new HIV-1 RTs inhibitor (Compound #8) that is structurally unique and greatly effective against HIV-1 through chemical library screening and a medicinal chemistry program by analyzing the structure-activity relationship (SAR). Further analysis of molecular docking and mechanisms of action demonstrated that Compound #8 is a novel type of HIV-1 non-nucleoside reverse transcriptase inhibitor (NNRTI) with a flexible binding mode. Therefore, it exhibits great therapeutic potential when combined with other existing HIV-1 drugs. Our current studies suggest that Compound #8 is a promising novel scaffold for the development of new HIV-1 treatments.

Original languageEnglish
Pages (from-to)1582-1592
Number of pages11
JournalACS Infectious Diseases
Volume9
Issue number8
DOIs
StatePublished - 11 Aug 2023

Bibliographical note

Publisher Copyright:
© 2023 American Chemical Society.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • HIV-1
  • NNRTI
  • novel chemical scaffold
  • phenotypic screening
  • reverse transcriptase
  • structure−activity relationship

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