It is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B. More
It is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B.
Valacyclovir
Valacyclovir; Valaciclovir; Valtrex; Zelitrex; Valacyclovir hydrochloride
Valamac, Valavir, Valcivir
2-[(2-amino-6-oxo-6,9-dihydro-3H-purin-9-yl)methoxy]ethyl (2S)-2-amino-3-methylbutanoate
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). It is converted to L-valine and acyclovir. 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.
NA
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.
Headache, vomiting, diarrhea, fainting, convulsion, confusion
Valacyclovir may interact with lithium, methotrexate, NSAIDs, immunosuppressive drugs, IV antibiotics, mesalamine, anti-viral drugs, anti-cancer drugs including cisplatin and carmustine.
Hypersensitivity
Store at 20-25°C.
324.3357
C13H20N6O4
124832-26-4