Substance

ID:460

Names and Identifiers
Synonyms
Valaciclovir HydrochloridevalaciclovirValacyclover HydrochloricValacyclovir HydrochlorideValacyclovirValaciclovirValaciclovir HclValacyclover Hydrochloride
IUPAC Traditional name
valaciclovir
Brand Name
ValtrexZelitrex
IUPAC name
2-[(2-amino-6-oxo-6,9-dihydro-3H-purin-9-yl)methoxy]ethyl (2S)-2-amino-3-methylbutanoate
Registration numbers
PubChem CID
CAS Number
PubChem SID
Properties
Physical Property
Hydrophobicity(logP)
-0.3
Molecule Details
Drug Groups
approved; investigational
Description
Valaciclovir (INN) or valacyclovir (USAN) is an antiviral drug used in the management of herpes simplex and herpes zoster (shingles). It is a prodrug, being converted in vivo to aciclovir. It is marketed by GlaxoSmithKline under the trade name Valtrex or Zelitrex. [Wikipedia]
Indication
For the treatment or suppression of cold sores (herpes labialis), herpes zoster (shingles), genital herpes in immunocompetent individuals, and recurrent genital herpes in HIV-infected individuals.
Pharmacology
Valaciclovir (INN) or Valacyclovir (USAN) is a prodrug and synthetic purine nucleoside analogue with inhibitory activity against herpes simplex virus types 1 (HSV-1), 2 (HSV-2), varicella-zoster virus (VZV), Epstein-Barr virus (EBV), and cytomegalovirus (CMV). Valaciclovir is almost completely converted to acyclovir and L-valine. The inhibitory activity of valaciclovir is highly selective due to its affinity for the enzyme thymidine kinase (TK) encoded by HSV and VZV. This viral enzyme converts acyclovir into acyclovir monophosphate, which is then converted into acyclovir diphosphate and triphosphate by cellular enzymes. Acyclovir is selectively converted to the active triphosphate form by cells infected with herpes viruses.
Toxicity
Adverse effects of overexposure might include headache and nausea.
Affected Organisms
Human Herpes Virus
Biotransformation
Valaciclovir is rapidly and almost entirely (~99%) converted to the active compound, acyclovir, and L-valine by first-pass intestinal and hepatic metabolism by enzymatic hydrolysis. Neither valaciclovir nor acyclovir is metabolized by cytochrome P450 enzymes.
Absorption
After oral administration, valaciclovir hydrochloride is rapidly absorbed from the gastrointestinal tract. The absolute bioavailability of acyclovir after administration of valaciclovir is 54.5% ± 9.1%.
Half Life
2.5-3.3 hours
Protein Binding
13-18%
Elimination
Acyclovir accounted for 89% of the radioactivity excreted in the urine.
Clearance
* Renal cl=255 +/- ?86 mL/min [healthy]
* apparent cl=86.3 +/- 21.3 mL/min/1.73?m2 [dialysis patients]
* apparent cl=679.16 +/- 162.76 mL/min/1.73?m2 [healthy]
References
• O'Brien JJ, Campoli-Richards DM: Acyclovir. An updated review of its antiviral activity, pharmacokinetic properties and therapeutic efficacy. Drugs. 1989 Mar;37(3):233-309. [Pubmed]
Molecular Spectra
No Data Available
Click here to submit data
References
• O'Brien JJ, Campoli-Richards DM: Acyclovir. An updated review of its antiviral activity, pharmacokinetic properties and therapeutic efficacy. Drugs. 1989 Mar;37(3):233-309. Pubmed