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The metabolic fate of α- and β-L-aspartyl-[U-(14)C]glycine was investigated in normal young rats in vivo and in vitro. The radioactive dipeptides were synthesized from L-aspartic acid and [U-(14)C]glycine in our laboratory. When labeled β-aspartylglycine was given intraperitoneally, about 66% of the dose was excreted in the urine and 8% was recovered in the(More)
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