Ambenonium
A long-acting cholinesterase inhibitor that prevents the breakdown of acetylcholine at the neuromuscular junction, used to treat myasthenia gravis, an autoimmune disease causing muscle weakness. By maintaining higher levels of acetylcholine at nerve-muscle connections, it improves muscle strength and endurance in affected individuals.
الوزن الجزيئي
537,6000 g/mol
LogP
5,10
TPSA
58,20 Ų
قاعدة ليبينسكي للخمسة
راسب
آلية العمل
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)
Blocks neuromuscular transmission at the motor end plate by competing with acetylcholine for nicotinic receptor binding sites, producing skeletal muscle relaxation and paralysis.
البنية ثنائية الأبعاد
Cite this structure
Embed this structure
SMILES
CC[N+](CC)(CCNC(=O)C(=O)NCC[N+](CC)(CC)Cc1ccccc1Cl)Cc1ccccc1Cl
InChI
InChI=1S/C28H40Cl2N4O2/c1-5-33(6-2,21-23-13-9-11-15-25(23)29)19-17-31-27(35)28(36)32-18-20-34(7-3,8-4)22-24-14-10-12-16-26(24)30/h9-16H,5-8,17-22H2,1-4H3/p+2
Molecular Formula
C28H42Cl2N4O2+2
HBD / HBA
2 / 2
الروابط القابلة للدوران
14
الذرات الثقيلة
36
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.
الأسئلة الشائعة
A long-acting cholinesterase inhibitor that prevents the breakdown of acetylcholine at the neuromuscular junction, used to treat myasthenia gravis, an autoimmune disease causing muscle weakness. By maintaining higher levels of acetylcholine at nerve-muscle connections, it improves muscle strength and endurance in affected individuals.
Blocks neuromuscular transmission at the motor end plate by competing with acetylcholine for nicotinic receptor binding sites, producing skeletal muscle relaxation and paralysis.
Yes, Ambenonium is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1652. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 2131. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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