Indoprofen

CHEMBL15870 Phase 4 Onaylandı Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
281.3 g/mol
LogP
2.8
Phase
4

This NSAID was developed to treat pain and inflammation but was withdrawn from the market after reports of serious gastrointestinal bleeding and other adverse effects. It worked through the standard NSAID mechanism of inhibiting prostaglandin-producing enzymes.

Moleküler Ağırlık

281,3000 g/mol

LogP

2,80

TPSA

57,60 Ų

Lipinski RO5

Geçer

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

CC(C(=O)O)c1ccc(N2Cc3ccccc3C2=O)cc1

InChI

InChI=1S/C17H15NO3/c1-11(17(20)21)12-6-8-14(9-7-12)18-10-13-4-2-3-5-15(13)16(18)19/h2-9,11H,10H2,1H3,(H,20,21)

Molecular Formula

C17H15NO3

HBD / HBA

1 / 3

Döndürülebilir Bağlar

3

Ağır Atomlar

21

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

This NSAID was developed to treat pain and inflammation but was withdrawn from the market after reports of serious gastrointestinal bleeding and other adverse effects. It worked through the standard NSAID mechanism of inhibiting prostaglandin-producing enzymes.

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, Indoprofen 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). CHEMBL15870. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 3718. 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.