Edrophonium

CHEMBL1104 Phase 4 Approuvé Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
166.2 g/mol
LogP
1.8
Phase
4

A short-acting cholinesterase inhibitor used to diagnose myasthenia gravis and to reverse neuromuscular blockade after surgery. It temporarily increases the availability of acetylcholine at nerve-muscle junctions.

Masse moléculaire

166,2400 g/mol

LogP

1,80

TPSA

20,20 Ų

Règle des 5 de Lipinski

Conforme

Mécanisme d'action

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)

Mécanisme

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

Structure 2D

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SMILES

CC[N+](C)(C)c1cccc(O)c1

InChI

InChI=1S/C10H15NO/c1-4-11(2,3)9-6-5-7-10(12)8-9/h5-8H,4H2,1-3H3/p+1

Molecular Formula

C10H16NO+

HBD / HBA

1 / 1

Liaisons Rotatives

2

Atomes Lourds

12

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.

Foire aux questions

A short-acting cholinesterase inhibitor used to diagnose myasthenia gravis and to reverse neuromuscular blockade after surgery. It temporarily increases the availability of acetylcholine at nerve-muscle junctions.

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

Yes, Edrophonium 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). CHEMBL1104. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 3202. Chemical information database.

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

Avertissement médical

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.