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. 2009 May 12;11(2):353–363. doi: 10.1208/s12248-009-9111-6

Table III.

Key Biopharmaceutical and Pharmacokinetic Properties of Valacyclovir

Property Value Reference
S+Log P −0.95 Estimated by ADMET Predictor (Simulations Plus, Inc.)
Aqueous solubility (mg/mL) 174 Merck index
Passive jejunal permeability (cm/s) 0.03 × 10−4 Estimated from Caco-2 Papp (37)
pK a values Acid = 9.4 (45)
Base1 = 1.9
Base2 = 7.4
Clearance (L h−1 kg−1) 0.211 Fitted from 5 mg/kg i.v. infusion data
V c (L/kg) 0.216 Fitted from 5 mg/kg i.v. infusion data
K 12 (h−1) 1.31 Fitted from 5 mg/kg iv infusion data
K 21 (h−1) 0.87 Fitted from 5 mg/kg iv infusion data
First pass extraction (%) 34 Fixed across all five oral doses
Lumenal degradation (%/h) at pH = 5 2.69 (30)
Lumenal degradation (%/h) at pH = 6.5 40.4 (30)
Lumenal degradation (%/h) at pH = 7.5 80.6 (30)
In situ transporter K m (μM) 1200 (30)