FIELD: organic chemistry, medicine, pharmacy.
SUBSTANCE: invention discloses compounds of the formula (I) or their pharmaceutically acceptable salts wherein: dotted line means optional double bond; X1 means optionally substituted (C1-C12)-alkyl, (C3-C12)-cycloalkyl, phenyl, furanyl, thienyl, pyridyl, thiazolyl, 1H-indolyl group; X2 means -CHO, -CN, -(CH2)vOR13, -(CH2)vNR21R22 or -(CH2)vNHC(O)R21 wherein v = 0 or 1; or X1 means optionally substituted heterocyclic group condensed with benzene ring; X2 means hydrogen atom; or X1 and X2 form in common optional spiroheterocyclic group condensed with benzene ring; R1, R2, R3 and R4 mean independently hydrogen atom (H) and (C1-C6)-alkyl group, or (R2 and R4) can form in common alkylene bridge consisting of 1-3 carbon atoms; Z1 means substituted phenyl; Z2 means substituted phenyl; Z3 means hydrogen atom; or Z1, Z2 and Z3 in common with carbon atom to which they are bound form bicyclic saturated rings. Invention relates also to a pharmaceutical composition based on these compounds. Compounds elicit properties of agonist of nociceptive receptor ORL-1 and can be used in treatment of cough.
EFFECT: valuable medicinal properties of compounds.
10 cl, 4 dwg, 11 tbl, 13 ex
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Authors
Dates
2004-09-27—Published
1999-07-26—Filed