机译:Improving Drug Delivery While Tailoring Prodrug Activation to Modulate C max and C min by Optimization of (Carbonyl)oxyalkyl Linker-Based Prodrugs of Atazanavir
机译:Discovery of Substituted Di(pyridin-2-yl)-1,2,4-thiadiazol-5-amines as Novel Macrofilaricidal Compounds for the Treatment of Human Filarial Infections
机译:Fragment Libraries Designed to Be Functionally Diverse Recover Protein Binding Information More Efficiently Than Standard Structurally Diverse Libraries
机译:Discovery of Novel 7‑Hydroxy-5-oxo-4,5-dihydrothieno3,2‑bpyridine-6-carboxamide Derivatives with Potent and Selective Antifungal Activity against Cryptococcus Species
机译:Discovery of a Novel Small-Molecule Inhibitor Disrupting TRBP–Dicer Interaction against Hepatocellular Carcinoma via the Modulation of microRNA Biogenesis
机译:Beyond Retigabine: Design, Synthesis, and Pharmacological Characterization of a Potent and Chemically Stable Neuronal Kv7 Channel Activator with Anticonvulsant Activity