摘要:
Synthetic analogs of 2',5'-oligoadenylate wherein the aglycon, ribosyl moiety and/or terminal nucleoside have been modified are effective therapeutic agents, particularly against HIV infection. The analogs are utilized in compositions for the treatment of disorders characterized by 2-5A pathway defects.
摘要:
There are disclosed: a method of controlling viral infection in plants comprising administering an antiviral effective amount of the compound ( R p)-P-thioadenylyl-(2'-5')-( R p)-P-thioadenylyl-(2'-5')-adenosine, the 5'-monophosphate thereof, or a water-soluble salt of either compound; a conjugate of poly (L-lysine) and 2'-5'-phosporothioate oligoadenylate (for formula see claim 2); and a compound of the formula
wherein m is zero, 1, 2 or 3 and n is 2, and water-soluble salts thereof.
摘要:
Synthetic analogs of 2',5'-oligoadenylate wherein the aglycon, ribosyl moiety and/or terminal nucleoside have been modified are effective therapeutic agents, particularly against HIV infection. The analogs are utilized in compositions for the treatment of disorders characterized by 2-5A pathway defects.
摘要:
There are disclosed: a method of controlling viral infection in plants comprising administering an antiviral effective amount of the compound ( R p)-P-thioadenylyl-(2'-5')-( R p)-P-thioadenylyl-(2'-5')-adenosine, the 5'-monophosphate thereof, or a water-soluble salt of either compound; a conjugate of poly (L-lysine) and 2'-5'-phosporothioate oligoadenylate (for formula see claim 2); and a compound of the formula
wherein m is zero, 1, 2 or 3 and n is 2, and water-soluble salts thereof.