FIELD: medicine.
SUBSTANCE: invention refers to a compound of formula (I) where Q represents a bond, CH-NR3 R4, NR5 or oxygen atom; X represents CH or nitrogen atom; Y represents a bond, CH2, oxygen atom or NR6; Z represents CH or nitrogen atom; R1, R2 represent, independently, hydrogen, halogen; R3, R4 represent, independently, hydrogen, (C1-C6)-alkyl; R5 represents hydrogen, (C1-C6)-alkyl, (CO)R7, SO2- (C1-C6)-alkyl or benzyl; R6 represents hydrogen, (C1-C6)-alkyl; R7 represents (C1-C6)-alkyl, phenyl, benzyl, OR8 or NR9R10; R8 represents (C1-C6)-alkyl; R9 represents hydrogen, (C1-C6)-alkyl; R9 represents hydrogen, (C1-C6)-alkyl; R11, R12 represent, independently, hydrogen or (C1-C6)-alkyl; and to their pharmaceutically acceptable salts; provided when X represents nitrogen atom, Y cannot represent oxygen atom or NR6; and except for the compounds (E)-N-hydroxy-3-(4-{(E)-3-[4-(4-methylpiperazine-1-yl)phenyl]-3-oxopropenyl}phenyl) acrylamide; (E)-N-hydroxy-3-{4-[(E)-3-(4-moropholine-4-ylphenyl)-3-oxopropenyl] phenyl}acrylamide; (E)-3-(3-flour-4-[(E)-3-(4-morpholine-4-ylphenyl)-3-oxopropenyl]phenyl}-N-hydroxyacrylamide. Also, the invention refers to a method for producing the compounds of formula (I), to a pharmaceutical composition, as well as to application of one or more compounds of formula (I), (la), (lb), (Ic).
EFFECT: producing new biologically active compounds which exhibit histone deacetylase inhibitor activity.
21 cl, 53 ex, 10 tbl
Title | Year | Author | Number |
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NOVEL HISTONE DEACETYLASE INHIBITORS | 2005 |
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RU2425826C2 |
METHOD OF SYNTHESIS OF 2,3-PYRIDINE DICARBOXIMIDE AND INTERMEDIATE COMPOUND FOR ITS SYNTHESIS | 1997 |
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RU2185382C2 |
SULPHONAMIDETHIAZOLE PYRIDINE DERIVATIVES AS GLUCOKINASE ACTIVATORS, SUITABLE FOR TREATING TYPE-2 DIABETES | 2005 |
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Authors
Dates
2011-06-10—Published
2007-03-30—Filed