Triflusal
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Also known as SID11112328SID144203987
Summary
Triflusal (CHEMBL1332032) is a phase-3 clinical-stage small molecule (ATC B01AC18); indicated across 2 conditions including thrombotic disease.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Small molecule
- ATC class: B01AC18
- Indications: 2 conditions
- Clinical trials: 6
- Chemistry: 248.15 Da · C10H7F3O4
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1332032 |
| Name | Triflusal |
| Type | Small molecule |
| Max phase | 3 |
| FDA approved | no |
| PubChem CID | 9458 |
| ATC | B01AC18 |
| Molecular formula | C10H7F3O4 |
| Molecular weight | 248.15 |
| InChIKey | RMWVZGDJPAKBDE-UHFFFAOYSA-N |
SMILES: CC(=O)OC1=C(C=CC(=C1)C(F)(F)F)C(=O)O
IUPAC name: 2-acetyloxy-4-(trifluoromethyl)benzoic acid
Also known as: Triflusal, SID11112328, SID144203987, TRIFLUSAL, triflusal
Patent coverage: 836 distinct patent families (3,038 SureChEMBL compound mentions), from 3 matched compound structure(s). One matched structure accounts for 3,027 (100%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Broader ChEMBL bioactivity targets: 6 (assay-derived). Sample: Lysine-specific demethylase 4E, Ubiquitin carboxyl-terminal hydrolase 2, 15-hydroxyprostaglandin dehydrogenase [NAD(+)], Aldehyde dehydrogenase 1A1, Cytochrome P450 2C19, 3-hydroxyacyl-CoA dehydrogenase type-2.
Bioactivity
ChEMBL activities: 3 potent at pChembl ≥ 5 of 7 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| CYP2C19 | 5.4 | Potency | 3981 | nM | CHEMBL_ACT_4019292 |
| CYP2C19 | 5.4 | AC50 | 3981 | nM | CHEMBL_ACT_6064736 |
| USP2 | 5.3 | Potency | 5012 | nM | CHEMBL_ACT_4719762 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
2 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| thrombotic disease | 3 | MONDO:0000831 | HP:0004419 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 6.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 3 |
| PHASE2 | 3 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT01174693 | PHASE4 | COMPLETED | Comparison of Triflusal and Clopidogrel in Secondary Prevention of Stroke Based on the Genotyping |
| NCT01612273 | PHASE4 | COMPLETED | The Effect of Triflusal on Peripheral Microcirculation Dysfunction |
| NCT02616497 | PHASE4 | COMPLETED | ASpirin vs Triflusal for Event Reduction In Atherothrombosis Secondary Prevention (ASTERIAS) |
| NCT00162799 | PHASE2 | COMPLETED | Efficacy Pilot Study of Triflusal in the Attenuation of Insulin Resistance in Human Obesity |
| NCT02321852 | PHASE2 | COMPLETED | Influence of Triflusal on Cognitive Functions in Healthy Subjects |
| NCT02904109 | PHASE2 | COMPLETED | Influence of Triflusal on Cognitive Functions in Subjects Under Chronic Stress |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- Diseases: thrombotic disease