Amifampridine

CHEMBL354077 Phase 4 अनुमोदित Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
109.1 g/mol
LogP
-0.5
Phase
4

A potassium channel blocker that prolongs nerve action potentials, thereby increasing acetylcholine release at neuromuscular junctions, used to treat Lambert-Eaton myasthenic syndrome (LEMS), a rare autoimmune neuromuscular disorder. By compensating for the impaired nerve-to-muscle signaling caused by autoantibodies in LEMS, it improves muscle strength.

आणविक भार

109.1300 g/mol

LogP

-0.50

TPSA

64.90 Ų

लिपिंस्की RO5

उत्तीर्ण

चिकित्सीय क्षेत्र

क्रिया का तंत्र

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)

तंत्र

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

2D संरचना

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SMILES

Nc1ccncc1N

InChI

InChI=1S/C5H7N3/c6-4-1-2-8-3-5(4)7/h1-3H,7H2,(H2,6,8)

Molecular Formula

C5H7N3

HBD / HBA

2 / 3

घूर्णनीय बंधन

0

भारी परमाणु

8

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.

अक्सर पूछे जाने वाले प्रश्न

A potassium channel blocker that prolongs nerve action potentials, thereby increasing acetylcholine release at neuromuscular junctions, used to treat Lambert-Eaton myasthenic syndrome (LEMS), a rare autoimmune neuromuscular disorder. By compensating for the impaired nerve-to-muscle signaling caused by autoantibodies in LEMS, it improves muscle strength.

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

Yes, Amifampridine 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). CHEMBL354077. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 5918. Chemical information database.

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

चिकित्सा अस्वीकरण

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.