Design, Synthesis and Evaluation of Novel Pyrrolidinone-Based ACE2 Inhibitors: Preliminary Study

This study focuses on the rational design and synthesis of new pyrrolidinone derivatives aimed at inhibiting the ACE2 receptor, a key entry point for SARS-CoV-2. Building on structural insights from known inhibitors like MLN-4760, five compounds featuring a pyrrolidinone core, with some incorporating indole rings, were synthesized and characterized. Their inhibitory activity against ACE2 was evaluated in vitro, with compound 4 showing the most promising results, further confirmed through cytotoxicity assays and molecular docking studies. Docking analysis revealed favorable binding interactions within the ACE2 active site, supporting the potential of compound 4 as a therapeutic agent. These findings provide a foundation for future in vivo studies and highlight the potential development of novel therapeutics targeting ACE2-related diseases, including COVID-19.

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Publication Details

Journal
Applied Sciences
Published
2026-02-09
DOI
https://doi.org/10.3390/app16041718
Primary Topic
Pharmacological Receptor Mechanisms and Effects
Type
article
Field-Weighted Citation Impact
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article

Design, Synthesis and Evaluation of Novel Pyrrolidinone-Based ACE2 Inhibitors: Preliminary Study

Maria Francesca Armentano, Federica Giuzio, Carmela Saturnino, Francesca Finelli et al.
Applied Sciences
Pharmacological Receptor Mechanisms and Effects
article

Design, Synthesis and Evaluation of Novel Pyrrolidinone-Based ACE2 Inhibitors: Preliminary Study

Maria Francesca Armentano, Federica Giuzio, Carmela Saturnino, Francesca Finelli, Ilaria Nigro, Hussein El‐Kashef, Magnus Monné, Antonio Vassallo, Anna Caruso
article en

Abstract

This study focuses on the rational design and synthesis of new pyrrolidinone derivatives aimed at inhibiting the ACE2 receptor, a key entry point for SARS-CoV-2. Building on structural insights from known inhibitors like MLN-4760, five compounds featuring a pyrrolidinone core, with some incorporating indole rings, were synthesized and characterized. Their inhibitory activity against ACE2 was evaluated in vitro, with compound 4 showing the most promising results, further confirmed through cytotoxicity assays and molecular docking studies. Docking analysis revealed favorable binding interactions within the ACE2 active site, supporting the potential of compound 4 as a therapeutic agent. These findings provide a foundation for future in vivo studies and highlight the potential development of novel therapeutics targeting ACE2-related diseases, including COVID-19.

Applied SciencesVol. 16(4)
University of Salerno (IT), University of Basilicata (IT), Azienda Ospedaliera S.Giuseppe Moscati (IT), University of the Republic of San Marino (SM), Sphinx University (EG), Assiut University (EG)
Openalex Percentile: Top 62%
Pharmacological Receptor Mechanisms and Effects
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