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Viral 2’-deoxythymidine kinase

In the past, various serendipitous discoveries have capitalized on the differential expression of enzymes by host and viral infected cells. For example, the prodrug Acyclovir, used widely for the treatment of herpes simplex and herpes zoster infections, is selectively activated through phosphorylation by viral thymidine kinase to acyclovir monophosphate which is then converted to the triphosphate, which inhibits DNA polymerase, by host cellular enzymes. Similarly several 2, 3 -dideoxynucleoside analogs such as Zidovudine (azidothymidine, AZT) and 2, 3 -didehydro-3 -deoxythymidine (D4T) have potent antiviral activity against human immunodeficiency vims (HIV). These compounds are selectively phosphoiylated intracellularly to the 5 -triphosphate derivatives which inhibit the viral reverse transcriptase. [Pg.373]


See other pages where Viral 2’-deoxythymidine kinase is mentioned: [Pg.395]    [Pg.552]    [Pg.177]    [Pg.232]    [Pg.182]    [Pg.539]    [Pg.180]    [Pg.196]   
See also in sourсe #XX -- [ Pg.30 , Pg.395 ]

See also in sourсe #XX -- [ Pg.395 ]




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