FIELD: organic chemistry; pharmacology.
SUBSTANCE: group of inventions relates to the preparation of nucleos(t)ide analogs targeted at the liver. A compound of formula IVa or a pharmaceutically acceptable salt of the said compound, where R1 and R2 are independently selected from the group consisting of C1-C6 alkyl; or alternatively R1 and R2 together with the atoms to which they are attached form a four to ten-membered heterocycle with two oxygen atoms as heteroatoms, optionally substituted with C1-C6 alkyl; each R3 is independently selected from the group consisting of hydrogen and C1-C6 alkyl, optionally substituted with phenyl; each R6 is independently C1-C6 alkyl; m is 0, 1, 2 or 3; n is 1 or 2; and X is O (oxygen) or NH are revealed. In addition, pharmaceutical compositions for the treatment of HIV and viral liver infection, methods for treating HIV and viral liver infection, as well as a method for inhibiting viral replication in the hepatocyte are disclosed. In addition, the use of the disclosed compound for the preparation of a medicament for the treatment of a viral infection of the liver, as well as the use of the compound for the treatment of a viral infection of the liver, is described.
EFFECT: group of inventions provides effective treatment of viral infection of the liver and HIV by interfering with molecular pathways in the liver.
49 cl, 3 tbl, 62 ex
(IVa)
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Authors
Dates
2023-05-23—Published
2019-01-08—Filed