
Journal of Antibiotics p. 700 - 709 (1999)
Update date:2022-08-30
Topics:
Chiba, Hiroyuki
Agematu, Hitosi
Dobashi, Kazuyuki
Yoshioka, Takeo
The structures of rhodopeptins, novel antifungal peptides, were determined on the basis of physico-chemical analyses of the intact molecules and their acid hydrolysates. The structures of rhodopeptins C1, C2, C3, C4 and B5 were determined to be cyclo (-Gly-L-Orn-L-Val-3-amino-10 -methyldodecanoyl-), cyclo (-Gly-L-Orn-L-Ile-3-amino-10-methyldodecanoyl-), cyclo (-Gly-L-Orn-L-Val-3 -amino-12-methyltridecanoyl-), cyclo (-Gly-L-Orn-L-Val-3-amino-l2-methyltetradecanoyl-) and cyclo (-Gly-L-Lys-L-Val-3-amino-13-methyltetradecanoyl-), respectively. They are novel cyclic tetrapeptides containing a lipophilic β-amino acid.
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