FIELD: chemistry.
SUBSTANCE: invention relates to a novel compound of formula (Ie) having antiviral RNA activity, in particular picornavirus activity, for example, paraechovirus, cardiovirus, enterovirus, such as EV virus, Coxsackie, polyellitis, rhinovirus, and hepatitis virus. In formula (Ie) (Ie) R1 is methyl; each R2 is methoxy; R3 is methyl; m is integer from 0 to 2; each R4 is independently selected from C1-C6 alkyl, R12O, halogen atom, R13R14NC(O) -, R16C(O)N(R15)-, R17OC(O)-, R19S(O)2-, R20S (O)2N(H) -, NH2S (O)2-, R21C (O) -, N (R22) (R23) - and -O-; R12, R13, R14, R15, R22 and R23 are independently selected from H and C1-C6 alkyl; R16, R17, R19, R20 and R21 are independently selected from C1-6 alkyl; any alkyl is optionally substituted with one or more F atoms; or two R4, attached to adjacent atoms of cycle B, form together with atoms to which they are bonded, 5- or 6-member heterocyclic or carbocyclic ring or a benzene ring; cycle B is 5- or 6-member heteroaryl containing 1 or 2 heteroatoms selected from N, O and S; or cycle B is phenyl.
EFFECT: compound can be used for treating a viral infection, for example caused by a non-enveloped virus with single-stranded (+) RNA.
20 cl, 1 dwg, 6 tbl, 112 ex
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Authors
Dates
2019-05-29—Published
2015-01-21—Filed