| abstract |
The present invention relates to novel antiviral compounds, which are aryl 3-deazauridine analogues at the C3 position, to a method for synthesizing said compounds, as well as to the antiviral uses thereof. The compounds are of the general formula (I), where: R1 is a hydrogen atom or a C 2 -C 6 acyl, R2, R3, R4, R5 and R6 are independently selected from a hydrogen atom, a C 1 -C 6 alkyl, a C 1 -C 6 alkoxy, a halogen atom, a nitro grouping or a cyano grouping, provided that at least one of R2, R3, R4, R5 and R6 is not the hydrogen atom. The invention also relates to the pharmaceutically acceptable salts thereof, to the enantiomers or diastereomers thereof, or to the mixtures thereof. |