FIELD: organic chemistry, peptides, pharmacy. SUBSTANCE: invention describes new lipopeptide derivatives of the formula (I) where R1 means OH or NH2; R2 means linear or branched, saturated or unsaturated, aliphatic C8-C22-acyl residue that can be broken by phenyl groups or oxygen atom, and their pharmaceutically acceptable salts. They are derivatives of antibiotics of lipopeptide complex A1437. Invention describes also a method of their synthesis and a pharmaceutical composition based on compounds of the formula (I). EFFECT: improved method of synthesis, new lipopeptides. 7 cl, 4 tbl, 72 ex
Authors
Dates
1999-11-27—Published
1995-03-29—Filed