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Molecular cloning of a widely expressed human homologue for the Drosophila trp gene

Precision synthesis ensures that 0.5mg dosed is 0.5mg delivered to the target receptor, not 0.3mg of active peptide plus 0.2mg of fragmented analogs

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Application of FMOs Inhibitors FMOs are monooxygenase that oxygenates nucleophilic heteroatom-containing chemicals and drugs and converts them into harmless, polar metabolites that are easily excreted (Krueger and Williams, 2005)