Diclofenac Sodium

CHEMBL1034 Phase 4 已批准 Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
318.1 g/mol
LogP
Phase
4

The sodium salt and most common oral formulation of diclofenac, an NSAID used for chronic inflammatory conditions including rheumatoid arthritis, osteoarthritis, and ankylosing spondylitis. Extended-release tablets allow twice-daily dosing.

分子量

318.1000 g/mol

TPSA

52.20 Ų

治疗领域

作用机制

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)

机制

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.

二维结构

SVG PNG

Cite this structure


                        

Embed this structure


                        

SMILES

O=C([O-])Cc1ccccc1Nc1c(Cl)cccc1Cl.[Na+]

InChI

InChI=1S/C14H11Cl2NO2.Na/c15-10-5-3-6-11(16)14(10)17-12-7-2-1-4-9(12)8-13(18)19;/h1-7,17H,8H2,(H,18,19);/q;+1/p-1

Molecular Formula

C14H10Cl2NNaO2

HBD / HBA

1 / 3

可旋转键数

4

重原子数

20

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.

常见问题

The sodium salt and most common oral formulation of diclofenac, an NSAID used for chronic inflammatory conditions including rheumatoid arthritis, osteoarthritis, and ankylosing spondylitis. Extended-release tablets allow 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, Diclofenac Sodium 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). CHEMBL1034. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 5018304. Chemical information database.

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

医疗免责声明

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.