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Fragmentation pathways may involve cleavage at amide bonds, producing characteristic fragment ions corresponding to partial backbone structures

TB-500s primary mechanism operates through G-actin sequestration by binding free G-actin monomers, TB-500 promotes cytoskeletal reorganisation that drives cell motility

Despite the absence of a statistically significant doseresponse relationship observed in this analysis, clinical decision-making should consider that absorption efficiencyrather than absolute dosagemay be the limiting factor

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Not assumed from a clean chromatogram