FIELD: medicine.
SUBSTANCE: in new compounds of formula (I): R1 is specified from the group including -OR7 and -NR8R9; where R7 means hydrogen; R8 and R9 are independently chosen from the group including hydrogen, aryl, substituted aryl containing one to three substitutes, preferentially one to two substitutes independently chosen from the group including alkenyl, substituted alkenyl containing one to three, preferentially one to two substitutes independently chosen from the group including carboxyl and carboxyl esters; R2 and R12 are independently chosen from the group including hydrogen, alkyl and alkyl substituted with 5-hydroxy-indolyl group; or R2 and R12 together with carbon atom whereto attached, form cycloalkyl group; R3 means hydrogen; each R4 independently means halogen; Q means oxygen; X means oxygen; R5 means alkylene; R6 is specified from the group consisting of substituted aryl containing one to three, preferentially one to two substitutes independently chosen from group consisting of acylamino, aryl, substituted aryl, containing one to three, preferentially from one to two substitutes chosen from halogen; and n is equal 0 to 3; or to its pharmaceutically acceptable salts. Besides the invention concerns a pharmaceutical composition, to the method of treatment or prevention of virus infections in mammals.
EFFECT: production of the new biologically active compound active with respect to treatment of virus infections in mammals, partially mediated with a member of flaviviridae virus family.
12 cl, 5 ex
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Authors
Dates
2009-12-10—Published
2004-06-04—Filed