Pifoxime

CHEMBL1998966 Phase 4 Aprovado 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.

Peso Molecular

276,3300 g/mol

LogP

1,80

TPSA

62,10 Ų

Regra dos 5 de Lipinski

Aprovado

Mecanismo de Ação

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)

Mecanismo

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

Estrutura 2D

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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

Ligações Rotacionáveis

4

Átomos Pesados

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.

Perguntas frequentes

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.

Aviso Médico

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.