Design, Synthesis, and Biological Evaluation of Benzimidazole Derivatives as Potential Lassa Virus Inhibitors

• Published in: Molecules (Basel, Switzerland) Vol. 28; no. 4; p. 1579
• Main Authors: Chen, Jinwei, Xu, Likun, Wang, Baogang, Zhang, Dongna, Zhao, Liangliang, Bei, Zhuchun, Song, Yabin
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.02.2023; MDPI
• Subjects: Antiviral activity; Antiviral agents; benzimidazole derivatives; Benzimidazoles; Binding; Design; Disease; Drugs; Fever; glycoprotein complex; Hemorrhage; Hemorrhagic fever; Infections; Inhibitors; Lassa fever; Lassa virus; Lead compounds; Lipophilic; Mortality; Peptides; Proteins; pseudovirus; RNA polymerase; Safety margins; Surface plasmon resonance; Viruses; glycoprotein complex; pseudovirus; Lassa virus; surface plasmon resonance; benzimidazole derivatives
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules28041579

The Lassa virus (LASV) causes Lassa fever, a highly infectious and lethal agent of acute viral hemorrhagic fever. At present, there are still no effective treatments available, creating an urgent need to develop novel therapeutics. Some benzimidazole compounds targeting the arenavirus envelope glycoprotein complex (GPC) are promising inhibitors of LASV. In this study, we synthesized two series of LASV inhibitors based on the benzimidazole structure. Lentiviral pseudotypes bearing the LASV GPC were established to identify virus entry inhibitors. Surface plasmon resonance (SPR) was further used to verify the binding activities of the potential compounds. Compounds , , , , and showed relatively excellent antiviral activities with IC values ranging from 7.58 to 15.46 nM and their SI values above 1251. These five representative compounds exhibited stronger binding affinity with low equilibrium dissociation constants (K < 8.25 × 10 M) in SPR study. The compound displayed the most potent antiviral activity (IC = 7.58 nM) with a relatively high SI value (2496), which could be further studied as a lead compound. The structure-activity relationship indicated that the compounds with lipophilic and spatially larger substituents might possess higher antiviral activity and a much larger safety margin. This study will provide some good guidance for the development of highly active compounds with a novel skeleton against LASV.