FIELD: organic chemistry, medicine, pharmacy, biochemistry. SUBSTANCE: invention relates to substituted azethidinones of the general formula (I) given in description. Compound of the formula (I) is synthesized by interaction of compound of the formula (II) with H-Y -NR7R8-. Compound of the formula (I) is a powerful inhibitor of human leukocyte elastase activity and can be used as anti-inflammatory and antidegenerative agent. EFFECT: improved method of synthesis, valuable pharmacological properties of compound. 33 cl, 10 tbl, 2 dwg, 26 ex
Authors
Dates
2000-04-27—Published
1993-10-26—Filed