FIELD: medicine, pharmaceutics.
SUBSTANCE: invention relates to 2-methyl-4-phenyl-5-oxo-1,4,5,6,7,8-hexahydrochinoline derivatives of formula 1 , in which R1 represents (1-6C)alkyl; R2 represents halogen; R3 represents SO2NR5R6 or (1-4C)alkoxy; X represents O or NR7; R4 represents R8-(2-8C)alkyl, R8-(3-8C)alkenyl or R8-(2-4C)alkoxy-(2-4C)alkyl; Z represents CN or NO2; R5 and R6 independently on each other represent H or (1-4C)alkyl; or R5 together with R6 and N, to which they are bound, form 5-6-member saturated ring, optionally containing additional heteroatom, selected from O; R8 represents OH, (1-4C)alkoxy, NH2; NR9C(O)R11, NR9SO2R11 or C(O)NR9R10; R7 and R9 independently represent H or (1-4C)alkyl; R10 represents (1-4C)alkyl; R11 represents (1-4C)alkyl, (1-4C)alkoxy(1-4C)alkyl, (3-6C)cycloalkyl, (1-4C)alkoxy or phenyl, or (4-5C)heteroaryl, and (4-5C)heteroaryl stands for aromatic group, which has 4-5 carbon atoms and at least one heteroatom, selected from N and O; or to their pharmaceutically acceptable salts. Invention also relates to pharmaceutical composition, as well as to application of 2-methyl-4-phenyl-5-oxo-1,4,5,6,7,8-hexahydrochinoline derivatives.
EFFECT: obtaining novel biologically active compounds, possessing agonistic activity with respect to FSH receptor.
8 cl, 33 ex
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Authors
Dates
2010-11-10—Published
2006-05-02—Filed