Pifoxime

CHEMBL1998966 Phase 4 承認済み Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
276.3 g/mol
LogP
1.8
Phase
4

Pifoxime is an oxime derivative with cholinesterase reactivating properties that was investigated as a treatment for organophosphate poisoning by regenerating inhibited acetylcholinesterase at neuromuscular junctions and in the central nervous system. Its clinical development was limited relative to pralidoxime, which became the standard oxime reactivator in organophosphate toxicity management.

分子量

276.3300 g/mol

LogP

1.80

TPSA

62.10 Ų

リピンスキーの五則

適合

作用機序

Blocks neuromuscular transmission at the motor end plate by competing with acetylcholine for nicotinic receptor binding sites, producing skeletal muscle relaxation and paralysis.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

機序

Blocks neuromuscular transmission at the motor end plate by competing with acetylcholine for nicotinic receptor binding sites, producing skeletal muscle relaxation and paralysis.

2D構造

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SMILES

C/C(=N\O)c1ccc(OCC(=O)N2CCCCC2)cc1

InChI

InChI=1S/C15H20N2O3/c1-12(16-19)13-5-7-14(8-6-13)20-11-15(18)17-9-3-2-4-10-17/h5-8,19H,2-4,9-11H2,1H3/b16-12+

Molecular Formula

C15H20N2O3

HBD / HBA

1 / 4

回転可能結合数

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.

よくある質問

Pifoxime is an oxime derivative with cholinesterase reactivating properties that was investigated as a treatment for organophosphate poisoning by regenerating inhibited acetylcholinesterase at neuromuscular junctions and in the central nervous system. Its clinical development was limited relative to pralidoxime, which became the standard oxime reactivator in organophosphate toxicity management.

Blocks neuromuscular transmission at the motor end plate by competing with acetylcholine for nicotinic receptor binding sites, producing skeletal muscle relaxation and paralysis.

Yes, Pifoxime 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). CHEMBL1998966. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 35755. Chemical information database.

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

医学的免責事項

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.