Foscarnet
Pyrophosphate Analog DNA Polymerase Inhibitor — ANTIINFECTIVES FOR SYSTEMIC USE
Also known as: foscarnet sodium, foscarnet sodium hydrate, foscavir, phosphonocarboxylic acid, phosphonoformic acid
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 class | Pyrophosphate Analog DNA Polymerase Inhibitor |
Molecular targets (4)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Reverse transcriptase/RNaseH | pol | unknown | IC50 5.69 |
| DNA polymerase catalytic subunit | UL54 | unknown | IC50 5.60 |
| Reverse transcriptase | reverse transcriptas | unknown | IC50 5.60 |
| DNA polymerase catalytic subunit | — | inhibitor | IC50 4.13 |
Regulatory approvals (2)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2019-03-26 | PMDA | — | CLINIGEN K.K. | |
| 1991-09-27 | FDA | — | CLINIGEN HLTHCARE |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
J05AD01 | ANTIINFECTIVES 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 term | LLR |
|---|---|
| Drug resistance | 1493.2 |
| Pathogen resistance | 784.7 |
| Nephropathy toxic | 644.6 |
| Cytomegalovirus viraemia | 603.0 |
| Off label use | 525.4 |
| Cytomegalovirus infection reactivation | 498.5 |
| Cytomegalovirus infection | 485.0 |
| Encephalitis cytomegalovirus | 473.5 |
| Cystitis haemorrhagic | 395.5 |
| Pancytopenia | 360.7 |
| BK virus infection | 353.3 |
| Renal impairment | 307.2 |
Chemical structure
Full physicochemical, ADMET and 3D-structure analysis of Foscarnet is on its molecule page.
| Molecular formula | CH3O5P |
|---|---|
| Molecular weight | 126.00 g/mol |
| CAS number | — |
| InChIKey | ZJAOAACCNHFJAH-UHFFFAOYSA-N |
| PubChem CID | 3415 |
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.
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Sources
- DrugCentral drug card 1241 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL666 — compound record and bioactivity
- PubChem CID 3415 — chemical identifiers
- DrugBank DB00529 — drug record
- FDA UNII 364P9RVW4X — substance identity
- DailyMed: FDA labels for Foscarnet — current prescribing information (label search)
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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