Dexibuprofen
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Also known as (s)-ibuprofenDexibuprofeneDexibuprofenoNSC-759814S-ibuprofenSeractilS(+)-IbuprofenSID11111293SID11111294SID11112775SID50106464SID85231335SID90340840SID47193724SID50100253SID144206692(S,+) Ibuprofenibuprofen-(s)(S)-(+)-Ibuprofen
Summary
Dexibuprofen (CHEMBL175) is an approved small-molecule non-narcotic analgesic (ATC M01AE14); indicated across 3 conditions including rheumatic disorder.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: M01AE14
- Indications: 3 conditions
- Clinical trials: 6
- Chemistry: 206.28 Da · C13H18O2
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL175 |
| Name | Dexibuprofen |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 39912 |
| ChEBI | CHEBI:43415 |
| ATC | M01AE14 |
| Molecular formula | C13H18O2 |
| Molecular weight | 206.28 |
| InChIKey | HEFNNWSXXWATRW-JTQLQIEISA-N |
SMILES: C[C@@H](C1=CC=C(C=C1)CC(C)C)C(=O)O
IUPAC name: (2S)-2-[4-(2-methylpropyl)phenyl]propanoic acid
Pharmacological roles (ChEBI): non-narcotic analgesic, non-steroidal anti-inflammatory drug.
Also known as: (s)-ibuprofen, Dexibuprofen, Dexibuprofene, Dexibuprofeno, NSC-759814, S-ibuprofen, Seractil, (S)-ibuprofen, S(+)-Ibuprofen, SID11111293, SID11111294, SID11112775
Parent form; salt/anhydrous children: CHEMBL1778537
Patent coverage: 3,300 distinct patent families (12,118 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 12,114 (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: 13 (assay-derived). Sample: Prelamin-A/C, RecQ-like DNA helicase BLM, Endonuclease 4, Peripheral myelin protein 22, Thyrotropin receptor, Interleukin-8 receptors, CXCR1/CXCR2, Prostaglandin G/H synthase 1, Prostaglandin G/H synthase 2, Prostaglandin G/H synthase 1, Cytochrome P450 2C9.
Bioactivity
ChEMBL activities: 18 potent at pChembl ≥ 5 of 27 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| BLM | 8.55 | Potency | 2.8 | nM | CHEMBL_ACT_4742002 |
| BLM | 8.55 | Potency | 2.8 | nM | CHEMBL_ACT_4913956 |
| PTGS1 | 7.01 | IC50 | 98.65 | nM | CHEMBL_ACT_8017611 |
| CXCR1 | 7 | IC50 | 100 | nM | CHEMBL_ACT_1492270 |
| PTGS1 | 6.98 | IC50 | 105 | nM | CHEMBL_ACT_7685382 |
| P0A6C1 | 6.6 | Potency | 251.2 | nM | CHEMBL_ACT_4084644 |
| PTGS2 | 6.14 | IC50 | 730 | nM | CHEMBL_ACT_8017613 |
| P05979 | 5.83 | IC50 | 1480 | nM | CHEMBL_ACT_8017741 |
| P79208 | 5.82 | IC50 | 1500 | nM | CHEMBL_ACT_3436572 |
| P05979 | 5.65 | IC50 | 2260 | nM | CHEMBL_ACT_777586 |
| PTGS2 | 5.61 | IC50 | 2460 | nM | CHEMBL_ACT_22789191 |
| LMNA | 5.6 | Potency | 2512 | nM | CHEMBL_ACT_3644595 |
| TSHR | 5.6 | Potency | 2512 | nM | CHEMBL_ACT_3921019 |
| TSHR | 5.6 | Potency | 2512 | nM | CHEMBL_ACT_4618229 |
| PTGS1 | 5.58 | IC50 | 2600 | nM | CHEMBL_ACT_2460290 |
| P05979 | 5.5 | IC50 | 3200 | nM | CHEMBL_ACT_3436604 |
| P05979 | 5.35 | IC50 | 4500 | nM | CHEMBL_ACT_22789174 |
| P05979 | 5.3 | IC50 | 4960 | nM | CHEMBL_ACT_22789241 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
3 indications (1 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 |
|---|---|---|---|
| rheumatic disorder | 4 | MONDO:0005554 | EFO:0005755 |
2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 6.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE1 | 3 |
| PHASE4 | 1 |
| PHASE3 | 1 |
| PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT01066676 | PHASE4 | COMPLETED | Dexibuprofen 400 mg Sachet Versus Ibuprofen 400 mg Sachet in Patients With Osteoarthritis of the Hip or Knee |
| NCT00812422 | PHASE3 | COMPLETED | The Efficacy and Safety of Dexibuprofen Syrup |
| NCT03852459 | PHASE2 | COMPLETED | Controlled Study to Assess the Efficacy and Safety of S-Ibuprofen Topical Gel 5% (AP0302) in the Treatment of DOMS |
| NCT00442585 | PHASE1 | COMPLETED | S(+)-Ibuprofen Effects on Asprin Treated Volunteers |
| NCT02956512 | PHASE1 | COMPLETED | Phase I Study to Evaluate the Safety of Dexibuprofen 300mg Under Fasting and Fed Conditions |
| NCT02956525 | PHASE1 | COMPLETED | Phase I Study to Evaluate the Safety of Dexibuprofen 200mg Under Fasting and Fed Conditions |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- Diseases: rheumatic disorder