Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Pival toxicity

Figure 8.21 The antiviral agent adefovir dipivoxil, a POM ester, is converted by esterase into its active component, adefovir. Two molecules of formaldehyde and two of pivalic acid are produced for each molecule of drug, the pivalic acid actually being a bigger concern for toxicity than formaldehyde. Figure 8.21 The antiviral agent adefovir dipivoxil, a POM ester, is converted by esterase into its active component, adefovir. Two molecules of formaldehyde and two of pivalic acid are produced for each molecule of drug, the pivalic acid actually being a bigger concern for toxicity than formaldehyde.
For more about the toxicity of pivalic acid, another common prodrug byproduct, see Brass, E.P. Pivalate-generating prodrugs and carnitine homeostasis in man. Pharmacol. Rev. 2002, 54, 589-598. [Pg.351]


See other pages where Pival toxicity is mentioned: [Pg.778]    [Pg.218]    [Pg.882]    [Pg.1193]    [Pg.371]    [Pg.122]    [Pg.130]    [Pg.102]   
See also in sourсe #XX -- [ Pg.378 , Pg.379 ]




SEARCH



Pival

Pivalate

Pivalates

© 2024 chempedia.info