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Biokhimiia ; 59(10): 1535-43, 1994 Oct.
Artigo em Russo | MEDLINE | ID: mdl-7819395

RESUMO

A review of synthetic methods of peptide substrates containing aminonaphthalenesulphonamide (ANSA) as the detected leaving group is presented. Variations of aminoacylic and peptide ANSA derivatives using ANSA as the C-protect group at all stages of the peptide synthesis, condensations of the ANSA with the N-protected peptide fragment obtained preliminary, the application of aminoacyl-ANSA as syntones are discussed. The synthesis scheme used while determining optimal ANSA substrates that involves reactions of aminoacyl derivatives of aminonaphthalenesulfonylchlorides with amines is shown. The application of di-tert-butylpyrocarbonate, DCC, chlorodimethylformiminium chloride, alkylchloroformate as condensing agents is described. The protection of amino groups was carried out by using Boc- and Cbz- groups.


Assuntos
Naftalenossulfonato de Anilina/síntese química , Compostos Cromogênicos/síntese química , Endopeptidases/metabolismo , Naftalenossulfonato de Anilina/metabolismo , Compostos Cromogênicos/metabolismo , Mapeamento de Peptídeos , Especificidade por Substrato
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