Author:
Mercorelli Beatrice,Desantis Jenny,Celegato Marta,Bazzacco Alessandro,Siragusa Lydia,Benedetti Paolo,Eleuteri Michela,Croci Federico,Cruciani Gabriele,Goracci Laura,Loregian Arianna
Cited by
10 articles.
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1. Design, synthesis, and biological evaluation of first-in-class indomethacin-based PROTACs degrading SARS-CoV-2 main protease and with broad-spectrum antiviral activity;European Journal of Medicinal Chemistry;2024-02
2. Medicinal chemistry strategies towards the development of non-covalent SARS-CoV-2 Mpro inhibitors;Acta Pharmaceutica Sinica B;2024-01
3. Design, Synthesis, and Biological Evaluation of Trisubstituted Piperazine Derivatives as Noncovalent Severe Acute Respiratory Syndrome Coronavirus 2 Main Protease Inhibitors with Improved Antiviral Activity and Favorable Druggability;Journal of Medicinal Chemistry;2023-11-22
4. An efficient eco-friendly, simple, and green synthesis of some new spiro-N-(4-sulfamoyl-phenyl)-1,3,4-thiadiazole-2-carboxamide derivatives as potential inhibitors of SARS-CoV-2 proteases: drug-likeness, pharmacophore, molecular docking, and DFT exploration;Molecular Diversity;2023-11-09
5. Discovery of PLpro and Mpro Inhibitors for SARS-CoV-2;ACS Omega;2023-06-14