| Weight | 324.341 g/mol |
|---|---|
| Formula | C13H20N6O4 |
| Hydrogen Acceptors | 9 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 7 |
valacyclovir (124832-26-4, 124832-27-5)
Score:
#111 in Microbiology
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#1214 in Biology
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#1391 in Chemistry
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- Valacyclovir for the prevention of cytomegalovirus disease after renal transplantation (The New England Journal of Medicine, 1999)
- Once-Daily Valacyclovir to Reduce the Risk of Transmission of Genital Herpes (The New England Journal of Medicine, 2004)
- Methylprednisolone, Valacyclovir, or the Combination for Vestibular Neuritis (The New England Journal of Medicine, 2004)
- Valacyclovir: a substrate for the intestinal and renal peptide transporters PEPT1 and PEPT2. (Biochemical and Biophysical Research Communications, 1998)
- Direct Evidence for Peptide Transporter (PepT1)-Mediated Uptake of a Nonpeptide Prodrug, Valacyclovir (Biochemical and Biophysical Research Communications, 1998)
- Antiviral therapy for herpes zoster: randomized, controlled clinical trial of valacyclovir and famciclovir therapy in immunocompetent patients 50 years and older. (Archives of Family Medicine, 2000)
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- Pubchem - valacyclovir
- Wikipedia - valacyclovir
Valaciclovir, also spelled valacyclovir, is an antiviral drug used in the management of herpes simplex, herpes zoster (shingles), and herpes B. It is a prodrug, being converted in vivo to aciclovir. Valaciclovir was approved for medical use in 1995.
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