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While AA derivatives consist of a chemical blocking group added to an alpha-amino group or a modified acyl group in a specific free AA, AA analogs are developed by replacing the alpha-amino group with a non-nitrogenous group (Schwab, 1995)

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both systolic and diastolic), body mass index (BMI), fibrinolytic activity, waist-hip ratio, and enzymatic activity (catalase [CAT], superoxide dismutase [SOD], and glutathione peroxidase [GPx])

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