Diclofenac Potassium

CHEMBL1200804 Phase 4 已批准 Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
334.2 g/mol
LogP
Phase
4

The potassium salt of diclofenac, a faster-absorbing oral NSAID formulation used for acute pain conditions including primary dysmenorrhea, migraine, and postoperative pain. The potassium salt dissolves more rapidly than the sodium salt.

分子量

334.2000 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

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SMILES

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

InChI

InChI=1S/C14H11Cl2NO2.K/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

C14H10Cl2KNO2

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 potassium salt of diclofenac, a faster-absorbing oral NSAID formulation used for acute pain conditions including primary dysmenorrhea, migraine, and postoperative pain. The potassium salt dissolves more rapidly than the sodium salt.

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 Potassium 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). CHEMBL1200804. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 23667642. 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.