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ACS Medicinal Chemistry Letters|May 16, 2022
Discovery of 2-Phenylquinolines with Broad-Spectrum Anti-coronavirus ActivityMaria Giulia Nizi, Leentje Persoons, Angela Corona, et al.
Journal of Medicinal Chemistry|May 29, 2019
Synthesis and Structure-Activity Relationships of 3,5-Disubstituted-pyrrolo[2,3- b]pyridines as Inhibitors of Adaptor-Associated Kinase 1 with Antiviral ActivitySven Verdonck, Szu-Yuan Pu, Fiona J Sorrell, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|May 26, 2022
The discovery of Zika virus NS2B-NS3 inhibitors with antiviral activity via an integrated virtual screening approachMuhammad Usman Mirza, Ida Alanko, Michiel Vanmeert, et al.
The Journal of Clinical Investigation|February 28, 2017
Anticancer kinase inhibitors impair intracellular viral trafficking and exert broad-spectrum antiviral effectsElena Bekerman, Gregory Neveu, Ana Shulla, et al.
Steroids|July 27, 2024
Steroidal 21-imidazolium salt derivatives: Synthesis and anticancer activityNatalia S Sucman, Dmitri Ya Bilan, Sergiu V Cojocari, et al.
Antiviral Research|June 23, 2022
Numb-associated kinases are required for SARS-CoV-2 infection and are cellular targets for antiviral strategiesMarwah Karim, Sirle Saul, Luca Ghita, et al.
Journal of Medicinal Chemistry|February 20, 2026
Antiviral Profiling and Cellular Activation of Carbobicyclic Nucleoside AnaloguesStephan Scheeff, Joan Marie Javillo Baguio, Benny Zhibin Liang, et al.
Ebiomedicine|September 27, 2021
The combined treatment of Molnupiravir and Favipiravir results in a potentiation of antiviral efficacy in a SARS-CoV-2 hamster infection modelRana Abdelnabi, Caroline S Foo, Suzanne J F Kaptein, et al.
Chemmedchem|April 10, 2026
2-Phenylquinolines Exhibit Anti-Severe Acute Respiratory Syndrome Coronavirus-2 Activity Through the Nonstructural Protein 13 Helicase InhibitionGiada Cernicchi, Maria Giulia Nizi, Roberta Emmolo, et al.
Mbio|January 10, 2023
The Substitutions L50F, E166A, and L167F in SARS-CoV-2 3CLpro Are Selected by a Protease Inhibitor In Vitro and Confer Resistance To NirmatrelvirDirk Jochmans, Cheng Liu, Kim Donckers, et al.
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