Less Cytotoxic Protoflavones as Antiviral Agents: Protoapigenone 1′-O-isopropyl ether Shows Improved Selectivity Against the Epstein–Barr Virus Lytic CycleMáté Vágvölgyi(University of Szeged), Attila Hunyadi(University of Szeged)International Journal of Molecular SciencesDecember 12, 201910.3390/ijms20246269Cited by 9SaveCiteExport RISWatch citationsRelated PapersLess Cytotoxic Protoflavones as Antiviral Agents: Protoapigenone 1′-O-isopropyl Ether Shows Improved Selectivity Against the Epstein-Barr Virus Lytic Cycle|Preprints.org|2019|7