Skip to content

Foscarnet

Pyrophosphate Analog DNA Polymerase Inhibitor — ANTIINFECTIVES FOR SYSTEMIC USE

Also known as: foscarnet sodium, foscarnet sodium hydrate, foscavir, phosphonocarboxylic acid, phosphonoformic acid

OfpFDA approvedPMDA approvedATC J05AD01

Data last refreshed: (DrugCentral release 2024-11-01)

Key facts

Foscarnet is an ofp drug in the Pyrophosphate Analog DNA Polymerase Inhibitor class catalogued in DrugCentral. It was first approved by the FDA in 1991. Its mechanism of action is classified as Chelating Activity and DNA Polymerase Inhibitors. DrugCentral lists 4 molecular targets, including pol, UL54 and reverse transcriptas. Recorded indications include Acyclovir-Resistant Mucocutaneous HSV in Immunocompromised Patients, CMV Retinitis in AIDS Patients and Encephalitis caused by human herpesvirus 6 infection.

  • Approval status: ofp (first approved 1991 by the FDA).
  • Drug class: Pyrophosphate Analog DNA Polymerase Inhibitor.
  • Mechanism of action: Chelating Activity; DNA Polymerase Inhibitors.
  • Molecular targets: pol, UL54, reverse transcriptas and DNA polymerase catalytic subunit (4 listed in DrugCentral).
  • Indications: Acyclovir-Resistant Mucocutaneous HSV in Immunocompromised Patients, CMV Retinitis in AIDS Patients and Encephalitis caused by human herpesvirus 6 infection.
  • ATC code: J05AD01 (Phosphonic acid derivatives).
  • Molecular formula: CH3O5P; molecular weight 126.00 g/mol.

Indications & contraindications

Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).

Indications (3)

  • Acyclovir-Resistant Mucocutaneous HSV in Immunocompromised Patients
  • CMV Retinitis in AIDS Patients
  • Encephalitis caused by human herpesvirus 6 infection

Off-label uses (4)

  • Acyclovir-Resistant HSV Infections
  • CMV-Related Polyradiculopathy in AIDS Patients
  • Herpes zoster associated with AIDS
  • Prevention of Cytomegalovirus Disease

Contraindications (14)

  • Anemia
  • Congenital long QT syndrome
  • Dehydration
  • Epilepsy
  • Granulocytopenic disorder
  • Hyperphosphatemia
  • Hypocalcemia
  • Hypokalemia
  • Hypomagnesemia
  • Hypophosphatemia
  • Kidney disease
  • Neutropenic disorder
  • Prolonged QT interval
  • Torsades de pointes

Mechanism & targets

Mechanism of action (MoA)Chelating Activity; DNA Polymerase Inhibitors
Established pharmacologic classPyrophosphate Analog DNA Polymerase Inhibitor

Molecular targets (4)

TargetGeneActionActivity
Reverse transcriptase/RNaseHpolunknownIC50 5.69
DNA polymerase catalytic subunitUL54unknownIC50 5.60
Reverse transcriptasereverse transcriptasunknownIC50 5.60
DNA polymerase catalytic subunit—inhibitorIC50 4.13

Regulatory approvals (2)

DateAgencyMarketed asApplicantOrphan
2019-03-26PMDA—CLINIGEN K.K.
1991-09-27FDA—CLINIGEN HLTHCARE

ATC classification

ATC codeTherapeutic hierarchy
J05AD01ANTIINFECTIVES FOR SYSTEMIC USE › ANTIVIRALS FOR SYSTEMIC USE › DIRECT ACTING ANTIVIRALS › Phosphonic acid derivatives

Reported adverse-event signals

Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.

MedDRA termLLR
Drug resistance1493.2
Pathogen resistance784.7
Nephropathy toxic644.6
Cytomegalovirus viraemia603.0
Off label use525.4
Cytomegalovirus infection reactivation498.5
Cytomegalovirus infection485.0
Encephalitis cytomegalovirus473.5
Cystitis haemorrhagic395.5
Pancytopenia360.7
BK virus infection353.3
Renal impairment307.2

Chemical structure

Full physicochemical, ADMET and 3D-structure analysis of Foscarnet is on its molecule page.

Molecular formulaCH3O5P
Molecular weight126.00 g/mol
CAS number—
InChIKeyZJAOAACCNHFJAH-UHFFFAOYSA-N
PubChem CID3415
OC(=O)P(O)(O)=O

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

What is Foscarnet used for?

DrugCentral lists the following indications for Foscarnet: Acyclovir-Resistant Mucocutaneous HSV in Immunocompromised Patients, CMV Retinitis in AIDS Patients and Encephalitis caused by human herpesvirus 6 infection.

How does Foscarnet work?

Foscarnet is classified as Chelating Activity and DNA Polymerase Inhibitors; its molecular targets in DrugCentral include pol, UL54, reverse transcriptas and DNA polymerase catalytic subunit (inhibitor).

When was Foscarnet first approved?

Foscarnet was first approved by the FDA in 1991.

What drug class does Foscarnet belong to?

Foscarnet is in the Pyrophosphate Analog DNA Polymerase Inhibitor class.

What is the chemical formula of Foscarnet?

Foscarnet has the molecular formula CH3O5P and a molecular weight of 126.00 g/mol.

Browse: all drugs starting with F · drug guides by category · protein targets A–Z.

Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

Quick facts

StatusOFP
First approval1991-09-27
AgencyFDA
Targets4
Indications3
FormulaCH3O5P
DrugCentral ID1241
Interactive profile