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2000
Volume 14, Issue 1
  • ISSN: 0929-8665
  • E-ISSN: 1875-5305

Abstract

Sites of exendin-4 that that are relatively susceptible to degradation in plasma were identified with the aim of providing information for designing new exendin-4 analogues. The stability of exendin-4 in human plasma was evaluated in vitro. The results showed that the peptide was slowly degraded with a half-life of 9.57 h and the principal cleavage sites are between Thr5 and Phe6, Phe6 and Thr7, and Thr7 and Ser8 of the N-terminus region of exendin-4.

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/content/journals/ppl/10.2174/092986607779117272
2007-01-01
2025-05-25
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