FIELD: peptides. SUBSTANCE: product: derivatives of peptides of the general formula (I):
where: R1 - free phenyl or phenyl substituted with halogen or lower alkoxy; benzofuryl; pyridyl or indolyl; R2 - hydrogen or lower alkyl; R3 - lower unsubstituted alkyl or alkyl substituted 1-3 times with halogen; amino; lower alkanesulfonylamino; carboxy (lower) alkoxy; unsubstituted or esterified halogen, lower alkoxy, nitro; R4 - lower alkyl; R5 - phenyl (lower) alkyl; R7 - hydrogen; lower alkyl; halogen; A - hydroxy- or didehydroxyproline; Y - bond, lower alkylene, lower alkenylene or their pharmaceutically acceptable salts. Reagent 1: HAN(R2)CH(CH2C6H5R3R7)CONR4R5. Reagent 2: R1-Y-COOH. In the synthesized product ester group R3 is removed or nitro-group in radical R3 is reduced. Pharmaceutical composition has pharmaceutically acceptable carrier and compound of the formula (I) as an active agent at amount 0.1-1000 mg as a single dose. Method of treatment of diseases intermediary agent of that is tachikinin involves prescription to patient the compound of the formula (I) at dose 0.1-1000 mg/day. EFFECT: improved method of synthesis, enhanced effectiveness of treatment. 9 tbl
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Authors
Dates
1997-02-20—Published
1991-10-23—Filed