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N-acyl substituted 7-amino-4-chloroisocoumarin: a peptide degradation model via an imide mechanism.

par Garino, Cédrik;Bihel, Frederic;Souard, Florence ;Quéléver, Gilles;Kraus, Jean-Louis
Référence Bioorganic & medicinal chemistry letters, 14, 7, page (1771-1774)
Publication Publié, 2004-04

Article révisé par les pairs

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Résumé :

During the coupling reaction between 3-alkoxy-7-amino-4-chloroisocoumarin and N-acyl alanine dipeptide, an unexpected deamidation reaction was observed. The proposed mechanism for this reaction involved the formation of an imide intermediate which after cleavage led to the release of amino acid moiety. The described deamidation reaction represents the first chemical model involving a non-peptidic moiety, which mimics biological and chemical deamidation processes occurring in proteins or peptides incorporating an asparagine or a glutamine residue.