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Updated: Sep 18, 2025

Quantitative Structure-Activity Relationship, Activity Prediction, and Molecular Dynamics of Non-nucleotide Reverse Transcriptase Inhibitors
Published on: May 9, 2025
Discovery and SAR exploration of novel nanomolar 3,4-dihydroquinazolin-2(1H)-one non-nucleoside reverse transcriptase
Eline Goffin1, Laurynn Torfs1, Fanos Tsingis1
1KU Leuven, Rega Institute for Medical Research, Laboratory of Medicinal Chemistry, Herestraat 49 - box 1041, 3000, Leuven, Belgium.
Abstract:
HIV continues to affect people every day and is still considered a global pandemic. Due to the absence of a cure or a vaccine, patients are subjected to a life-long treatment that is often complicated by antiviral drug resistance, highlighting the need to develop new therapies. One of the key targets for this antiviral drug development is reverse transcriptase. In this paper, we describe the discovery, synthesis and biological evaluation of a novel chemotype of potent 3,4-dihydroquinazolin-2(1H)-one non-nucleoside reverse transcriptase inhibitors (NNRTIs). Several compounds exhibit nanomolar antiviral activity against wild-type (WT) human immunodeficiency virus-1 (HIV-1) and maintain an excellent activity profile against various clinically relevant mutations. These promising first results provide an exciting foundation for further research into this novel NNRTI scaffold.

