FIELD: medicine, pharmaceutics.
SUBSTANCE: given invention refers to drugs containing compounds of specified structural formulae or to their pharmaceutically acceptable salts. Besides, the invention refers to pharmaceutical compositions for treating a host infected by hepatitis B virus, on the basis of each of said compounds separately (or their pharmaceutically acceptable salt), and also in their combination with an effective amount of a compound chosen from a group consisting of β-L-2-hydroxymethyl-5-(cytosine-1-yl)-1,3-oxathiolane (3TC), cys-2-hydroxymethyl-5-(5-fluorocytosine-5-yl)-1,3-oxathiolane (FTC), β-L-2'-fluor-5-methyl-arabinofuranosyl-uridine (L-FMAU), β-D-2,6-diaminopurindioxolane (DAPD), famciclovir, penciclovir, 2-amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)2-methylenecyclopentyl]-6H-purine-6-one (entecavir, BMS-200475), 9-[2-(phosphono-methoxy)ethyl]adenine (PMEA, adefovir, dipivoxyl), lobucavir, ganciclovir and ribavirin.
.
EFFECT: creation of the drug for treating a host infected by hepatitis B virus.
12 cl, 6 tbl, 4 dwg, 11 ex
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