FIELD: medicine, pharmaceutics.
SUBSTANCE: present invention refers to heterocyclylsubstituted imidazole derivatives of general formula or to its pharmaceutically acceptable salts wherein R1 stands for a group of formula where * stands for a position whereon a carbonyl group is bound, R4 stands for phenyl or pyridyl, and phenyl or pyridyl can be substituted by one substitute where the substitute is chosen from a group including haloid, nitrogroup, cyanogroup, trifluoromethyl, (C1-C6)alkyl and (C1-C6)alkoxygroup, R6 and R7 stands for hydrogen, R2 stands for (C1-C6)alkyl, and alkyl can be substituted by a substitute where the substitute is chosen from a group including (C3-C6)cycloalkyl and (C6)aryl where aryl can be substituted by a trifluoromethyl substitute, R3 stands for phenyl, and phenyl can be substituted by substitutes in number 1 to 2 independently chosen from a group including haloid, trifluoromethyl, trifluoromethoxygroup, difluoromethoxygroup, trifluoromethylthiogroup and (C1-C6)alkyl. Also, the invention refers to methods for producing compounds of formula I, to a drug prepared of the compound of formula I, to applying the compound of formula I for preparing the drug and to a method of controlling cytomegalovirus infection.
EFFECT: production of new imidazole derivatives exhibiting antiviral activity, particularly in relation to cytomegaloviruses.
10 cl, 4 tbl, 31 ex
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Authors
Dates
2011-04-10—Published
2006-02-14—Filed