Foscarmet
Brand names,
Foscarmet
Analogs
Foscarmet
Brand Names Mixture
Foscarmet
Chemical_Formula
CH3O5P
Foscarmet
RX_link
http://www.rxlist.com/cgi/generic2/foscarnet.htm
Foscarmet
fda sheet
Foscarmet
msds (material safety sheet)
Foscarmet
Synthesis Reference
Noren, Jan O.; et al., J.Med.Chem. 26(2) 264-270(1983)
Foscarmet
Molecular Weight
126.005 g/mol
Foscarmet
Melting Point
88.06 oC
Foscarmet
H2O Solubility
Complete
Foscarmet
State
Solid
Foscarmet
LogP
No information avaliable
Foscarmet
Dosage Forms
Injection
Foscarmet
Indication
For the treatment of CMV retinitis in patients with acquired immunodeficiency syndrome (AIDS) and for treatment of acyclovir-resistant mucocutaneous HSV infections in immunocompromised patients.
Foscarmet
Pharmacology
Foscarnet is an organic analogue of inorganic pyrophosphate that inhibits replication of herpes viruses in vitro including cytomegalovirus (CMV) and herpes simplex virus types 1 and 2 (HSV-1 and HSV-2). Foscarnet does not require activation (phosphorylation) by thymidine kinase or other kinases and therefore is active in vitro against HSV TK deficient mutants and CMV UL97 mutants. Thus, HSV strains resistant to acyclovir or CMV strains resistant to ganciclovir may be sensitive to foscarnet. However, acyclovir or ganciclovir resistant mutants with alterations in the viral DNA polymerase may be resistant to foscarnet and may not respond to therapy with foscarnet. The combination of foscarnet and ganciclovir has been shown to have enhanced activity in vitro.
Foscarmet
Absorption
Poorly absorbed after oral administration (bioavailability from 12 to 22%).
Foscarmet
side effects and Toxicity
Oral, rat LD50: >2,000 mg/kg. Signs of overdose include renal impairment.
Foscarmet
Patient Information
Foscarmet
Organisms Affected
Human herpes viruses