FIELD: microbiology. SUBSTANCE: present invention describes compounds of formula I given in the claims wherein RI is hydrogen atom, or unsubstituted or substituted alkyl group, and A is number of cyclic or acyclic nitrogen containing groups. Said compounds are useful antibiotics and resistant to dehydropeptidase I in vivo. Present invention also describes methods of preparing said compounds and methods of use thereof. EFFECT: improved properties of the title compounds. 31 cl 9 tbl
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