Cyclic peptides. XVIII. Syntheses of AM-toxin I analogs containing bulky L-amino acid residues instead of an L-alanine*

Autor: Nobuo Izumiya, Tetsuo Kato, Sannamu Lee, Hisakazu Mihara, Tamio Ueno, Haruhiko Aoyagi
Rok vydání: 2009
Předmět:
Zdroj: International Journal of Peptide and Protein Research. 25:144-148
ISSN: 0367-8377
DOI: 10.1111/j.1399-3011.1985.tb02157.x
Popis: In order to investigate the influence of the alanine residue at position 1 of AM-toxin I (cyclic tetradepsipeptide) on necrotic activity for apple leaves, three analogs, [l-2-aminobutanoic acid1] AM-toxin I, [l-leucine1] AM-toxin I and [l-phenylalanine1] AM-toxin I, were synthesized by the conventional method for peptide synthesis. Spectra of 1H-n.m.r., u.v. and CD of the analogs were similar to those of natural AM-toxin I. The analogs showed appreciable biological activity including host-specificity, indicating that considerable variation in the size of side chain at position 1 is allowed for the induction of necrotic activity.
Databáze: OpenAIRE