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Selective phosphorylation spectrum

Tenofovir disoproxil fumarate is hydrolyzed rapidly to tenofovir and then is phosphorylated by cellular kinases to its active metabohte, tenofovir diphosphate the active moiety is, in fact, a triphosphate compound because the parent drug starts out as the monophosphate. The intracellular diphosphate is a competitive inhibitor of viral reverse transcriptases and is incorporated into HIV DNA to cause chain termination because it has an incomplete ribose ring. Although tenofovir diphosphate has broad-spectrum activity against viral DNA polymerases, it has low affinity for human DNA polymerases-a, -P, and -y, which is the basis for its selective toxicity. [Pg.675]


See other pages where Selective phosphorylation spectrum is mentioned: [Pg.108]    [Pg.356]    [Pg.69]    [Pg.356]    [Pg.116]    [Pg.356]    [Pg.297]    [Pg.328]    [Pg.961]    [Pg.963]    [Pg.524]    [Pg.526]    [Pg.33]    [Pg.30]    [Pg.233]    [Pg.358]    [Pg.20]    [Pg.28]    [Pg.339]    [Pg.359]    [Pg.134]    [Pg.222]    [Pg.335]    [Pg.144]    [Pg.328]    [Pg.549]    [Pg.488]   
See also in sourсe #XX -- [ Pg.23 , Pg.255 ]




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Selective phosphorylation

Selectivity phosphorylation

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