Alclofenac

CHEMBL94081 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
226.6 g/mol
LogP
2.5
Phase
4

A nonsteroidal anti-inflammatory drug (NSAID) that reduces pain and inflammation by inhibiting prostaglandin synthesis. Though largely withdrawn from many markets due to hypersensitivity concerns, it was used for arthritis and musculoskeletal pain management.

Khối lượng phân tử

226,6500 g/mol

LogP

2,50

TPSA

46,50 Ų

Lipinski RO5

Đạt

Cơ chế tác dụng

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)

Cơ chế

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.

Cấu trúc 2D

SVG PNG

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SMILES

C=CCOc1ccc(CC(=O)O)cc1Cl

InChI

InChI=1S/C11H11ClO3/c1-2-5-15-10-4-3-8(6-9(10)12)7-11(13)14/h2-4,6H,1,5,7H2,(H,13,14)

Molecular Formula

C11H11ClO3

HBD / HBA

1 / 3

Liên kết có thể quay

5

Nguyên tử nặng

15

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.

Câu hỏi thường gặp

A nonsteroidal anti-inflammatory drug (NSAID) that reduces pain and inflammation by inhibiting prostaglandin synthesis. Though largely withdrawn from many markets due to hypersensitivity concerns, it was used for arthritis and musculoskeletal pain management.

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, Alclofenac 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). CHEMBL94081. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 30951. Chemical information database.

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

Tuyên bố miễn trách y tế

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.