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The drugs pharmacokinetics were characterized through interspecies scaling, and human pharmacokinetics were predicted using a population pharmacokinetic model integrating allometric scaling

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The researchers fed the mice: L-Tyrosine N-Acetyl L-Tyrosine L-Tyrosine Methyl Ester O-Phospho L-Tyrosine Researchers concluded that N-Acetyl-L-tyrosine was the least effective prodrug tested. [8] Here again, another myth of NALTs superiority has been shattered