Sulindac
Nonsteroidal Anti-inflammatory Drug — MUSCULO-SKELETAL SYSTEM
Also known as: clinoril, MK 231, MK-231, MK231
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Sulindac is an ofp drug in the Nonsteroidal Anti-inflammatory Drug class catalogued in DrugCentral. It was first approved by the FDA in 1978. Its mechanism of action is classified as Cyclooxygenase Inhibitors. DrugCentral lists 14 molecular targets, including AKR1B10, AKR1B1 and GLRA1. Recorded indications include Ankylosing spondylitis, Articular gout, Bursitis and Osteoarthritis.
- Approval status: ofp (first approved 1978 by the FDA).
- Drug class: Nonsteroidal Anti-inflammatory Drug.
- Mechanism of action: Cyclooxygenase Inhibitors.
- Molecular targets: AKR1B10, AKR1B1, GLRA1 and Akr1b1 (14 listed in DrugCentral).
- Indications: Ankylosing spondylitis, Articular gout, Bursitis, Osteoarthritis and Rheumatoid arthritis and others.
- ATC code: M01AB02 (Acetic acid derivatives and related substances).
- Molecular formula: C20H17FO3S; molecular weight 356.41 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (6)
- Ankylosing spondylitis
- Articular gout
- Bursitis
- Osteoarthritis
- Rheumatoid arthritis
- Tendinitis
Contraindications (23)
- Alcoholism
- Anemia
- Asthenia
- Blood coagulation disorder
- Breastfeeding (mother)
- Cardiovascular event risk
- Chronic heart failure
- Coronary artery bypass graft
- Disease of liver
- Disorder of cardiovascular system
- Disorder of connective tissue
- Edema
- Gastrointestinal hemorrhage
- Gastrointestinal perforation
- Gastrointestinal ulcer
- Hypertensive disorder
- Kidney disease
- Kidney stone
- Myocardial infarction
- Peptic ulcer
- Pregnancy, function
- Smokes tobacco daily
- Systemic lupus erythematosus
Mechanism & targets
| Mechanism of action (MoA) | Cyclooxygenase Inhibitors |
|---|---|
| Established pharmacologic class | Nonsteroidal Anti-inflammatory Drug |
Molecular targets (14)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Aldo-keto reductase family 1 member B10 | AKR1B10 | unknown | IC50 6.46 |
| Aldose reductase | AKR1B1 | unknown | IC50 6.43 |
| Glycine receptor subunit alpha-1 | GLRA1 | unknown | EC50 6.42 |
| Aldose reductase | Akr1b1 | unknown | IC50 6.36 |
| Complement C5 | C5 | unknown | Kd 6.24 |
| Prostaglandin G/H synthase 1 | PTGS1 | inhibitor | IC50 5.92 |
| Prostaglandin G/H synthase 1 | PTGS1 | unknown | IC50 4.80 |
| Peroxisome proliferator-activated receptor gamma | PPARG | unknown | EC50 4.64 |
| Prostaglandin G/H synthase 2 | PTGS2 | inhibitor | IC50 4.25 |
| Lactoylglutathione lyase | GLO1 | unknown | Ki 4.11 |
| Prostaglandin E synthase | PTGES | unknown | IC50 4.10 |
| Retinoic acid receptor RXR-alpha | RXRA | unknown | IC50 4.08 |
| Bile salt export pump | Abcb11 | unknown | IC50 4.06 |
| 72 kDa type IV collagenase | MMP2 | unknown | — |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 1978-09-27 | FDA | — | MERCK |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
M01AB02 | MUSCULO-SKELETAL SYSTEM › ANTIINFLAMMATORY AND ANTIRHEUMATIC PRODUCTS › ANTIINFLAMMATORY AND ANTIRHEUMATIC PRODUCTS, NON-STEROIDS › Acetic acid derivatives and related substances |
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 | 112.7 |
| Hangover | 68.5 |
| Musculoskeletal discomfort | 49.8 |
| Musculoskeletal chest pain | 41.0 |
| Skin disorder | 31.9 |
| Inflammatory pain | 30.7 |
| Neck pain | 27.7 |
| Nodal osteoarthritis | 27.6 |
| Crystal nephropathy | 26.0 |
| Accidental exposure to product | 25.1 |
| Gastric haemorrhage | 24.7 |
| Dry gangrene | 23.6 |
Chemical structure
| Molecular formula | C20H17FO3S |
|---|---|
| Molecular weight | 356.41 g/mol |
| CAS number | 38194-50-2 |
| InChIKey | MLKXDPUZXIRXEP-MFOYZWKCSA-N |
| PubChem CID | 1548887 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Sulindac used for?
DrugCentral lists the following indications for Sulindac: Ankylosing spondylitis, Articular gout, Bursitis, Osteoarthritis, Rheumatoid arthritis and Tendinitis.
How does Sulindac work?
Sulindac is classified as Cyclooxygenase Inhibitors; its molecular targets in DrugCentral include AKR1B10, AKR1B1, GLRA1 and Akr1b1.
When was Sulindac first approved?
Sulindac was first approved by the FDA in 1978.
What drug class does Sulindac belong to?
Sulindac is in the Nonsteroidal Anti-inflammatory Drug class.
What is the chemical formula of Sulindac?
Sulindac has the molecular formula C20H17FO3S and a molecular weight of 356.41 g/mol.
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Sources
- DrugCentral drug card 2534 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL15770 — compound record and bioactivity
- PubChem CID 1548887 — chemical identifiers
- DrugBank DB00605 — drug record
- FDA UNII 184SNS8VUH — substance identity
- DailyMed: FDA labels for Sulindac — current prescribing information (label search)
- UniProt O60218 (AKR1B10) — target protein
- UniProt P15121 (AKR1B1) — target protein
- UniProt P23415 (GLRA1) — target protein
- UniProt P01031 (C5) — target protein
- UniProt P23219 (PTGS1) — target protein
- UniProt P37231 (PPARG) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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