Rofecoxib
MUSCULO-SKELETAL SYSTEM
Also known as: ceeoxx, vioxx
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Rofecoxib is an ofm drug catalogued in DrugCentral. It was first approved by the FDA in 1999. DrugCentral lists 10 molecular targets, including Ptgs2, PTGER2 and PTGS2. Recorded indications include Dysmenorrhea, Juvenile rheumatoid arthritis, Migraine and Osteoarthritis.
- Approval status: ofm (first approved 1999 by the FDA).
- Molecular targets: Ptgs2, PTGER2, PTGS2 and PTGS2 (10 listed in DrugCentral).
- Indications: Dysmenorrhea, Juvenile rheumatoid arthritis, Migraine, Osteoarthritis and Pain and others.
- ATC code: M01AH02 (Coxibs).
- Molecular formula: C17H14O4S; molecular weight 314.36 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (6)
- Dysmenorrhea
- Juvenile rheumatoid arthritis
- Migraine
- Osteoarthritis
- Pain
- Rheumatoid arthritis
Mechanism & targets
Molecular targets (10)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Prostaglandin G/H synthase 2 | Ptgs2 | unknown | IC50 7.92 |
| Prostaglandin E2 receptor EP2 subtype | PTGER2 | unknown | Ki 7.47 |
| Prostaglandin G/H synthase 2 | PTGS2 | unknown | IC50 6.52 |
| Prostaglandin G/H synthase 2 | PTGS2 | inhibitor | IC50 6.51 |
| Prostaglandin G/H synthase 2 | PTGS2 | unknown | IC50 6.37 |
| Prostaglandin G/H synthase 2 | Ptgs2 | unknown | IC50 6.12 |
| Prostaglandin G/H synthase 1 | PTGS1 | unknown | IC50 5.77 |
| Cytochrome c oxidase subunit 2 | MT-CO2 | unknown | IC50 5.52 |
| Prostaglandin G/H synthase 1 | Ptgs1 | unknown | IC50 4.94 |
| Prostaglandin G/H synthase 1 | PTGS1 | unknown | IC50 4.63 |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 1999-05-20 | FDA | — | — |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
M01AH02 | MUSCULO-SKELETAL SYSTEM › ANTIINFLAMMATORY AND ANTIRHEUMATIC PRODUCTS › ANTIINFLAMMATORY AND ANTIRHEUMATIC PRODUCTS, NON-STEROIDS › Coxibs |
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 hypersensitivity | 614.5 |
| Oesophageal spasm | 255.3 |
| Acne cystic | 249.1 |
| Oesophageal pain | 239.8 |
| Lymphoedema | 181.1 |
| Stress | 175.2 |
| Drug intolerance | 172.7 |
| Drug ineffective | 150.5 |
| Sleep apnoea syndrome | 138.0 |
| Cystitis | 111.6 |
| Tinnitus | 107.6 |
| Anaphylactic reaction | 100.1 |
Chemical structure
Full physicochemical, ADMET and 3D-structure analysis of Rofecoxib is on its molecule page.
| Molecular formula | C17H14O4S |
|---|---|
| Molecular weight | 314.36 g/mol |
| CAS number | 162011-90-7 |
| InChIKey | RZJQGNCSTQAWON-UHFFFAOYSA-N |
| PubChem CID | 5090 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Rofecoxib used for?
DrugCentral lists the following indications for Rofecoxib: Dysmenorrhea, Juvenile rheumatoid arthritis, Migraine, Osteoarthritis, Pain and Rheumatoid arthritis.
How does Rofecoxib work?
Its molecular targets in DrugCentral include Ptgs2, PTGER2, PTGS2 and PTGS2 (inhibitor).
When was Rofecoxib first approved?
Rofecoxib was first approved by the FDA in 1999.
What is the chemical formula of Rofecoxib?
Rofecoxib has the molecular formula C17H14O4S and a molecular weight of 314.36 g/mol.
Browse: all drugs starting with R · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 2397 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL122 — compound record and bioactivity
- PubChem CID 5090 — chemical identifiers
- DrugBank DB00533 — drug record
- FDA UNII 0QTW8Z7MCR — substance identity
- DailyMed: FDA labels for Rofecoxib — current prescribing information (label search)
- UniProt P43116 (PTGER2) — target protein
- UniProt P35354 (PTGS2) — target protein
- UniProt P23219 (PTGS1) — target protein
- UniProt P00403 (MT-CO2) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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