A. Consider the Pharmacokinetic (PK) profiles of the NRTI below and 1. Discuss the structural basis for the observed PKs 2. Discuss any other Pharmacokinetic profiles that you think might be different. Remember to provide a structural basis for your reasoning. 3. Discus and account for the differences in clinical use (indications) and Toxicities of the drugs below. Table 1 In vitro activity and stability of TFV and its prodrugs TDF and TAF. EC 50 HIV-1 (μM) Half-life (min) TFV 5.0 TDF TAF 0.05 0.005 stable 0.41 90

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A. Consider the Pharmacokinetic (PK) profiles of the NRTI below and
1. Discuss the structural basis for the observed PKs
2. Discuss any other Pharmacokinetic profiles that you think might be different. Remember to
provide a structural basis for your reasoning.
3. Discus and account for the differences in clinical use (indications) and Toxicities of the
drugs below.
Table 1
In vitro activity and stability of TFV and its prodrugs TDF and TAF.
EC 50 HIV-1 (μM)
Half-life (min)
TFV
5.0
TDF
TAF
0.05
0.005
stable
0.41
90
Transcribed Image Text:A. Consider the Pharmacokinetic (PK) profiles of the NRTI below and 1. Discuss the structural basis for the observed PKs 2. Discuss any other Pharmacokinetic profiles that you think might be different. Remember to provide a structural basis for your reasoning. 3. Discus and account for the differences in clinical use (indications) and Toxicities of the drugs below. Table 1 In vitro activity and stability of TFV and its prodrugs TDF and TAF. EC 50 HIV-1 (μM) Half-life (min) TFV 5.0 TDF TAF 0.05 0.005 stable 0.41 90
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