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Valacyclovir hydrochloride

Cat. No. M5061
Valacyclovir hydrochloride Structure
Synonym:

Valaciclovir hydrochloride

Size Price Availability Quantity
10mg USD 60  USD60 In stock
50mg USD 90  USD90 In stock
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Quality Control & Documentation
Biological Activity

Valaciclovir inhibits the uptake of substrates of dipeptide transporters, such as cefalexin. The metabolism of Valaciclovir to Aciclovir probably occurs within the gut lumen prior to absorption, in the small intestine after uptake but before entry into the portal blood system, and in the liver before entry into systemic circulation.Valaciclovir, the L-valyl ester of acyclovir (ZOVIRAX), demonstrates good oral absorption and nearly complete conversion to acyclovir incynomolgus monkeys, indicating its suitability as an orally administered prodrug.

Chemical Information
Molecular Weight 360.8
Formula C13H21ClN6O4
CAS Number 124832-27-5
Form Solid
Solubility (25°C) DMSO 14 mg/ml
Water 72 mg/ml
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] MacDougall C,et.al. J Antimicrob Chemother. Pharmacokinetics of valaciclovir.

[2] de Miranda P,et.al. Drug Metab Dispos. Metabolic fate and pharmacokinetics of the acyclovir prodrug valaciclovir in cynomolgus monkeys.

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