FIELD: pharmaceutical industry. SUBSTANCE: present invention describes compounds of general formula I wherein at least one of R1, R2, R3 or R4 is wherein L is O or CH2; m is integer of 0 to 14 inclusive; n is integer of 0 to 14; p and q are independently integers of 0 to 10; each of R1, R2, R3 and R4 is independently -C(O)-(CH2)z, -C(O)-(CH2)xCH3;, -(CH2)z+1-C(OH)H-(CH2)xCH3, -C(O)-(CH2)z-G and (CH2)xCH3, wherein G is -S-(O)-; X is integer of 0 to 14; Z is integer of 0 to 10; each of A1 and A2 is independently OH, OCH3, -OP(O)(OH)2, -O-(CH2)d+1-OPO(OH)2, wherein d is independently integer of 0 to 5; X is (CH2)tO(CH2)vCH3, (CH2)tOPO(OH)2, wherein t and v are integers of 0 to 14; Y is OH, O(CH2)wCH3,, halogen atom, -OC(O)-(CH2)wCH3 wherein W is integer of 0 to 14, and pharmaceutically acceptable salts thereof. Compound I and pharmaceutically acceptable salts thereof have antiviral activity. Present invention describes intermediate compound and pharmaceutical composition. EFFECT: improved properties of the pharmaceutical composition. 21 cl
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