FIELD: chemistry.
SUBSTANCE: present invention relates to novel substituted 4(6)-bromine-5-hydroxy-1H-indol-3-yl acetic acids and their esters, their pharmaceutically acceptable salts and/or hydrates which have antiviral activity, particularly against influenza virus having general formula or : where: R1 is an amino group substitute selected from a hydrogen atom, C1-C5alkyl optionally substituted with a hydroxy group, mono- or di(C1-C5 alkyl)amino group; acyl which is benzoyl optionally substituted with a halogen; or sulphonyl which is (C1-C5alkyl)sulphonyl, phenylsulphonyl optionally substituted with a C1-C5alkyl group, phenyl-C1-C3 alkylsulphonyl, 6-member nitrogen-containing heteroarylsulphonyl; R2 is an alkyl substitute selected from a hydrogen atom, a halogen atom, hydroxyl, amino, mono-(C1-C5 alkyl)- or di(C1-C5 alkyl)amino group; R3 is hydrogen optionally substituted with C1-C5alkyl; R4 is a hydroxyl group substitute selected from a hydrogen atom, C1-C5alkyl, C1-C5acyl; R5 is cyclic system substitute selected from hydrogen or mono(C1-C5 alkyl)- or di(C1-C5 alkyl)aminomethylene group. The invention also relates to a focused library, a medicinal agent and a pharmaceutical composition.
EFFECT: obtaining of compounds with antiviral activity.
26 cl, 1 tbl, 18 ex
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Authors
Dates
2010-06-27—Published
2008-05-28—Filed