A Simple Method of Preparation of Labelled Peptides Possessing Antibiotic Properties

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Abstract
Preparation of derivatives of peptide antibiotics polymyxin B and colistin- substituted on free amino groups by aminoacyl residues is described. The first procedure is based on the condensation of the antibiotic with active ester of a suitably protected amino acid. The second one makes use of Woodward’s reagent by condensation of the antibiotic with a protected amino acid. The following compounds were prepared: glycyl-14C-polymyxin B and glutaminyl-polymyxin B and glycylcolistin, also under conditions suitable for a radioactive synthesis. All the preparations preserve a substantial part of the biological activity comparable with polymyxin B and colistin.

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