Mofezolac

CHEMBL259972 Phase 4 Approved Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
339.3 g/mol
LogP
3.1
Phase
4

This NSAID from Japan selectively inhibits the COX-1 enzyme to provide pain relief and anti-inflammatory effects, with a mechanism somewhat different from most NSAIDs that primarily target COX-2. It has been used to treat various pain conditions and inflammatory states.

Molecular Weight

339.3000 g/mol

LogP

3.10

TPSA

81.80 Ų

Lipinski RO5

Pass

Mechanism of Action

Inhibits cyclooxygenase (COX-1 and/or COX-2) enzymes, reducing the synthesis of prostaglandins and thromboxanes from arachidonic acid. This produces anti-inflammatory, analgesic, and antipyretic effects.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanism

Inhibits cyclooxygenase (COX-1 and/or COX-2) enzymes, reducing the synthesis of prostaglandins and thromboxanes from arachidonic acid. This produces anti-inflammatory, analgesic, and antipyretic effects.

2D Structure

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SMILES

COc1ccc(-c2noc(CC(=O)O)c2-c2ccc(OC)cc2)cc1

InChI

InChI=1S/C19H17NO5/c1-23-14-7-3-12(4-8-14)18-16(11-17(21)22)25-20-19(18)13-5-9-15(24-2)10-6-13/h3-10H,11H2,1-2H3,(H,21,22)

Molecular Formula

C19H17NO5

HBD / HBA

1 / 6

Rotatable Bonds

6

Heavy Atoms

25

No targets recorded

Target interaction data is not yet available for this drug.

No interactions recorded

Drug interaction data is not yet available for this compound.

No side effects recorded

Side effect data is not yet available for this drug.

Frequently Asked Questions

This NSAID from Japan selectively inhibits the COX-1 enzyme to provide pain relief and anti-inflammatory effects, with a mechanism somewhat different from most NSAIDs that primarily target COX-2. It has been used to treat various pain conditions and inflammatory states.

Inhibits cyclooxygenase (COX-1 and/or COX-2) enzymes, reducing the synthesis of prostaglandins and thromboxanes from arachidonic acid. This produces anti-inflammatory, analgesic, and antipyretic effects.

Yes, Mofezolac is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

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References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL259972. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 4237. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

Medical Disclaimer

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.