Diflunisal

CHEMBL898 Phase 4 Onaylandı Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
250.2 g/mol
LogP
4.4
Phase
4

An NSAID derived from salicylic acid, used to treat mild to moderate pain including that from osteoarthritis. It is metabolized differently from aspirin and does not produce the same level of antiplatelet effects. Its half-life is longer than aspirin, allowing twice-daily dosing.

Moleküler Ağırlık

250,2000 g/mol

LogP

4,40

TPSA

57,50 Ų

Lipinski RO5

Geçer

Terapötik Alanlar

Etki Mekanizması

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)

Mekanizma

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 Yapı

SVG PNG

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SMILES

O=C(O)c1cc(-c2ccc(F)cc2F)ccc1O

InChI

InChI=1S/C13H8F2O3/c14-8-2-3-9(11(15)6-8)7-1-4-12(16)10(5-7)13(17)18/h1-6,16H,(H,17,18)

Molecular Formula

C13H8F2O3

HBD / HBA

2 / 5

Döndürülebilir Bağlar

2

Ağır Atomlar

18

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.

Sıkça Sorulan Sorular

An NSAID derived from salicylic acid, used to treat mild to moderate pain including that from osteoarthritis. It is metabolized differently from aspirin and does not produce the same level of antiplatelet effects. Its half-life is longer than aspirin, allowing twice-daily dosing.

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

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL898. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 3059. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Tıbbi Sorumluluk Reddi

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.