Rapacuronium Bromide
Rapacuronium bromide is the bromide salt form of rapacuronium, a rapid-onset non-depolarizing neuromuscular blocking agent that was withdrawn from clinical use due to an unacceptable rate of severe bronchospasm. See rapacuronium for complete pharmacological details.
Masse moléculaire
677,8000 g/mol
TPSA
55,80 Ų
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)
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
Cite this structure
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SMILES
C=CC[N+]1([C@H]2C[C@H]3[C@@H]4CC[C@H]5C[C@H](OC(C)=O)[C@@H](N6CCCCC6)C[C@]5(C)[C@H]4CC[C@]3(C)[C@H]2OC(=O)CC)CCCCC1.[Br-]
InChI
InChI=1S/C37H61N2O4.BrH/c1-6-20-39(21-12-9-13-22-39)32-24-30-28-15-14-27-23-33(42-26(3)40)31(38-18-10-8-11-19-38)25-37(27,5)29(28)16-17-36(30,4)35(32)43-34(41)7-2;/h6,27-33,35H,1,7-25H2,2-5H3;1H/q+1;/p-1/t27-,28+,29-,30-,31-,32-,33-,35-,36-,37-;/m0./s1
Molecular Formula
C37H61BrN2O4
HBD / HBA
- / 6
Liaisons Rotatives
9
Atomes Lourds
44
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
Rapacuronium bromide is the bromide salt form of rapacuronium, a rapid-onset non-depolarizing neuromuscular blocking agent that was withdrawn from clinical use due to an unacceptable rate of severe bronchospasm. See rapacuronium for complete pharmacological details.
Blocks neuromuscular transmission at the motor end plate by competing with acetylcholine for nicotinic receptor binding sites, producing skeletal muscle relaxation and paralysis.
Yes, Rapacuronium Bromide 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). CHEMBL1200549. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 5311398. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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