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It is stable in human gastric juice for more than 24 hours — the property that made per-oral administration viable in its animal studies — and the published literature reports a defined cascade: VEGFR2 receptor activation, then Src/FAK and Akt, then eNOS and nitric-oxide bioavailability
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In this study, essential dynamics assessment was performed for each generated MD trajectory using Bio3d package (Released version 2.4-1
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