FIELD: organic synthesis and biologically-active compounds. SUBSTANCE: invention provides new pyrido[3,2-e] pyrazinones of general formula I: (I), wherein X, Y, and Z are nitrogen or group CR3, provided that at least one of X, Y, Z is nitrogen; R1 is optionally aryl- substituted C1-C10-alkyl; R2 hydrogen, C5-C7-cycloalkyl, or C1-C10-alkyl optionally substituted by radical selected from group including aryl, aryloxy, hydroxyl, sulfonyl, pyridyl, and quinolyl; A is methylene, group NR3, or oxygen atom; R3 hydrogen or C1-C6-alkyl; or their physiologically tolerable salts exhibiting anti-asthmatic and antiallergenic effects. EFFECT: increased choice of pharmaceutically active compounds. 8 cl, 2 tbl, 53 ex
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Authors
Dates
1999-12-27—Published
1996-03-25—Filed