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2000
Volume 16, Issue 4
  • ISSN: 0929-8665
  • E-ISSN: 1875-5305

Abstract

A series of aldehyde inhibitors with the general formula Ac-Phe-Val-Thr-X-CHO, where X = Lys, Arg, Phe, Tyr, p-nitro-L-phenylalanine (Nif), p-amino-L-phenylalanine (Amf), p-guanidine-L-phenylalanine (Gnf), pyridyl-L-alanine (Pal), was synthesized. The starting structure of this series based on our previous work on cathepsin G chromogenic substrates. The synthesis of all compounds was performed in solid phase applying Fmoc chemistry. We investigated the inhibitory potency of the obtained compounds against cathepsin G and bovine α-chymotrypsin and evaluated their dissociation constants (Ki). The studied peptides displayed different inhibition profiles and potency. As a result, a potent and selective inhibitor of cathepsin G with the sequence Ac-Phe-Val-Thr-Gnf-CHO, displaying Ki = 22 nM was obtained.

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/content/journals/ppl/10.2174/092986609787848144
2009-04-01
2025-10-19
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/content/journals/ppl/10.2174/092986609787848144
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  • Article Type:
    Research Article
Keyword(s): Cathepsin G; chymotrypsin; peptide aldehydes; peptidomimetics
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