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In an in vivo study, a quercetin metabolite (4,5-diacetyl-3,Y,7-trimethyl-quercetin), administered orally BID for 4 days protected mice against lethal infection by Coxsackie virus, promoting survival in a dose-response scale: 10, 20, and 40 mg/kg increased survival by 30, 40, and 50%, respectively ( in vitro ( Inhibition of Reverse Transcriptase Quercetin has been investigated in vitro as an antiviral agent for HIV due to its ability to inhibit crucial enzymes: reverse transcriptase (RT), integrase (IN), and protease (PR) (80)

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28 Several studies demonstrated a synergistic approach to inducing a rat model of T2DM