Ethionamide
Antimycobacterial — ANTIINFECTIVES FOR SYSTEMIC USE
Also known as: amidazine, ethioniamide
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Ethionamide is an ofm drug in the Antimycobacterial class catalogued in DrugCentral. It was first approved by the FDA in 1965. DrugCentral lists 3 molecular targets, including PPO2, katG and inhA. Recorded indications include Acute tuberculosis, Pulmonary Mycobacterium avium complex infection and Pulmonary tuberculosis.
- Approval status: ofm (first approved 1965 by the FDA).
- Drug class: Antimycobacterial.
- Molecular targets: PPO2, katG and inhA (3 listed in DrugCentral).
- Indications: Acute tuberculosis, Pulmonary Mycobacterium avium complex infection and Pulmonary tuberculosis.
- ATC code: J04AD03 (Thiocarbamide derivatives).
- Molecular formula: C8H10N2S; molecular weight 166.25 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (3)
- Acute tuberculosis
- Pulmonary Mycobacterium avium complex infection
- Pulmonary tuberculosis
Off-label uses (3)
- Atypical mycobacterial infection
- Leprosy
- Tuberculosis of meninges
Contraindications (5)
- Alcoholism
- Diabetes mellitus
- Disease of liver
- Hepatic failure
- Hypothyroidism
Mechanism & targets
| Established pharmacologic class | Antimycobacterial |
|---|
Molecular targets (3)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Polyphenol oxidase 2 | PPO2 | unknown | IC50 5.40 |
| Catalase-peroxidase | katG | unknown | — |
| Enoyl-[acyl-carrier-protein] reductase [NADH] | inhA | inhibitor | — |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 1965-04-30 | FDA | — | WYETH PHARMS INC |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
J04AD03 | ANTIINFECTIVES FOR SYSTEMIC USE › ANTIMYCOBACTERIALS › DRUGS FOR TREATMENT OF TUBERCULOSIS › Thiocarbamide 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 | 446.2 |
| Electrocardiogram QT prolonged | 195.2 |
| Neuropathy peripheral | 116.9 |
| Drug reaction with eosinophilia and systemic symptoms | 107.5 |
| Pathogen resistance | 89.5 |
| Urinary tract inflammation | 80.5 |
| Tuberculoma of central nervous system | 76.9 |
| Anaemia | 76.5 |
| Hepatitis cholestatic | 60.5 |
| Conductive deafness | 55.5 |
| Vomiting | 55.4 |
| Treatment failure | 48.6 |
Chemical structure
Full physicochemical, ADMET and 3D-structure analysis of Ethionamide is on its molecule page.
| Molecular formula | C8H10N2S |
|---|---|
| Molecular weight | 166.25 g/mol |
| CAS number | — |
| InChIKey | AEOCXXJPGCBFJA-UHFFFAOYSA-N |
| PubChem CID | 2761171 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Ethionamide used for?
DrugCentral lists the following indications for Ethionamide: Acute tuberculosis, Pulmonary Mycobacterium avium complex infection and Pulmonary tuberculosis.
How does Ethionamide work?
Its molecular targets in DrugCentral include PPO2, katG and inhA (inhibitor).
When was Ethionamide first approved?
Ethionamide was first approved by the FDA in 1965.
What drug class does Ethionamide belong to?
Ethionamide is in the Antimycobacterial class.
What is the chemical formula of Ethionamide?
Ethionamide has the molecular formula C8H10N2S and a molecular weight of 166.25 g/mol.
Browse: all drugs starting with E · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 1083 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1441 — compound record and bioactivity
- PubChem CID 2761171 — chemical identifiers
- DrugBank DB00609 — drug record
- FDA UNII OAY8ORS3CQ — substance identity
- DailyMed: FDA labels for Ethionamide — current prescribing information (label search)
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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