Naproxen Sodium

CHEMBL1200806 Phase 4 Disetujui Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
252.2 g/mol
LogP
Phase
4

This is the sodium salt form of naproxen that is absorbed more quickly, providing faster pain relief for the same conditions.

Berat Molekul

252,2400 g/mol

TPSA

49,40 Ų

Area Terapeutik

Mekanisme Kerja

Non-selective COX inhibitor.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mekanisme

Non-selective COX inhibitor.

Struktur 2D

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SMILES

COc1ccc2cc([C@H](C)C(=O)[O-])ccc2c1.[Na+]

InChI

InChI=1S/C14H14O3.Na/c1-9(14(15)16)10-3-4-12-8-13(17-2)6-5-11(12)7-10;/h3-9H,1-2H3,(H,15,16);/q;+1/p-1/t9-;/m0./s1

Molecular Formula

C14H13NaO3

HBD / HBA

- / 3

Ikatan yang Dapat Dirotasi

3

Atom Berat

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.

Pertanyaan yang Sering Diajukan

This is the sodium salt form of naproxen that is absorbed more quickly, providing faster pain relief for the same conditions.

Non-selective COX inhibitor.

Yes, Naproxen 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). CHEMBL1200806. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 23681059. Chemical information database.

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

Penyangkalan Medis

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.