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We validated previously reported pharmacokinetic parameters [48] in diabetic rats (i.e., elimination half-life, volume of distribution, bioavailability, and absorption rate) by conducting a 24-hour pharmacokinetic (PK) study following intravenous (IV) administration of a 20 g dose of Sema in a saline vehicle ( Table S1 )

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Ex-4 inhibits mTOR, an autophagy inhibitor in tumor cells, by downregulating Akt and simultaneously activating AMPK, subsequently attenuating the phosphorylation of its major downstream targets, eukaryotic translation initiation factor 4e binding protein 1(4E-BP1) and ribosomal s6 kinase 1(S6K1)