Figure 2
Figure 2. Ezatiostat (TLK199) pharmacokinetics. (A) Pharmacokinetic model of ezatiostat and metabolites. Formation of metabolites is assumed to be unidirectional. TLK199 undergoes de-esterification to both TLK235 and TLK236; however, because the quantity of TLK235 measured in this study is consistently less than the level of quantification, this pathway is ignored (dashed lines). TLK236 undergoes further de-esterification to TLK117. Both TLK199 and TLK236 can be eliminated via more than one pathway. However, this study provides no insight into the fraction of each entity eliminated by each pathway. (B) Concentration of primary active metabolite TLK236 by dose level. Error bars represent SD of the mean at each sampling time point. (C) Fed/fast pharmacokinetic concentration of the primary active metabolite TLK236.

Ezatiostat (TLK199) pharmacokinetics. (A) Pharmacokinetic model of ezatiostat and metabolites. Formation of metabolites is assumed to be unidirectional. TLK199 undergoes de-esterification to both TLK235 and TLK236; however, because the quantity of TLK235 measured in this study is consistently less than the level of quantification, this pathway is ignored (dashed lines). TLK236 undergoes further de-esterification to TLK117. Both TLK199 and TLK236 can be eliminated via more than one pathway. However, this study provides no insight into the fraction of each entity eliminated by each pathway. (B) Concentration of primary active metabolite TLK236 by dose level. Error bars represent SD of the mean at each sampling time point. (C) Fed/fast pharmacokinetic concentration of the primary active metabolite TLK236.

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