FIELD: medicine, pharmaceutics.
SUBSTANCE: invention refers to new indanone derivatives of formula I wherein the radicals A1-A4, D, E, X and G1-G4 have the values specified in the description, to their pharmaceutically acceptable salts or enantiomers, as well as to methods for producing them, and a pharmaceutical composition applicable for preventing and treating a viral disease and containing the above compounds as an active ingredient.
EFFECT: indanone derivatives possess the excellent inhibitory activity on picornaviruses, including Coxsackie viruses, entero-, echo-, polio- and rhinoviruses; it also possesses low cytotoxicity, and can be effective as an active ingredient of the pharmaceutical composition for preventing or treating a viral disease, including poliomyelitis, paralysis, acute haemorrhagic conjunctivitis, viral meningitis, hand-foot-and-mouth disease, vesicular fever, hepatitis A, myositis, myocarditis, pancreatitis, diabetes, epidemic myalgia, encephalitis, influenza, Coxsackie virus A disease, foot-and-mouth disease, asthma, chronic obstructive pulmonary disease, pneumonia, sinusitis or otitis media.
17 cl, 5 tbl, 307 ex
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Authors
Dates
2016-02-10—Published
2012-06-18—Filed