FIELD: organic chemistry, medicine, pharmacy. SUBSTANCE: invention relates to N-substituted aminotetralines of the formula (I): wherein R1 is taken independently among the group consisting of hydrogen atom, hydroxy-group, halogen atom, C1-8--alkoxy-group, substituted C1-8--alkoxy-group wherein substituent represents halogen atom; n = 0-2; Y represents methylene; m = 0-3; B1 represents hydrogen atom; B2 represents hydrogen atom; R2 is taken among the group consisting of hydrogen atom, hydroxy-group, C1-6-alkyl, C1-6-alkenyl, phenyl, substituted phenyl wherein substituent is taken among halogen atom, C1-6-alkyl, C1-6--alkoxy-group, trifluoro-C1-6-alkyl, nitro-group, naphthyl and pyridyl; L is taken among the group consisting of C1-8-alkylene, C1-4-alkylene-C3-7-cycloalkyl-C1-4-alkylene, C1-4--alkylenearyl-C1-4-alkylene; R3 is taken among phenyl, substituted phenyl where substituent is taken among halogen atom, nitro-group, C1-8-alkoxy-group, trifluoromethyl group and amino-C1-8-alkyl, naphthyl and thienyl; and their enantiomers, diastereoisomers and pharmaceutically acceptable salts. Compounds of the formula (I) are ligands of receptor Y5 of neuropeptide Y that allows their using in pharmaceutical composition for treatment of diseases and disorders associated with inhibition of subtype Y5 of receptor NPY. EFFECT: valuable medicinal properties of compounds. 20 cl, 3 tbl, 9 ex
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Authors
Dates
2003-12-20—Published
1999-04-12—Filed