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S.Antonic-BakerA.PitsillouE.LiangJ.FrenchC.HungA.et al (2022)
Oral bioavailability ranges from 1030% due to first-pass hepatic metabolism and gastric degradation, while subcutaneous injection achieves near-100% bioavailability with direct systemic distribution

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The classification of predicted targets showed that 28.0% were kinases, 26.0% enzymes, and 11.0% lyases (Supplementary Fig