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Structure-Based Design, Synthesis, and Biological Evaluation of Irreversible Human Rhinovirus 3C Protease Inhibitors. 8. Pharmacological Optimization of Orally Bioavailable 2-Pyridone-Containing

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1993 Annual report of the American Association of Poison Control Centers Toxic Exposure Surveillance System

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Binding profiles for oligoethylene glycols and oligoethylene glycol monomethyl ethers and an assessment of their abilities to catalyze phase-transfer reactions

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