Rocuronium Bromide
A bromide salt form of rocuronium with the same therapeutic properties. A neuromuscular blocking agent used during surgery and intubation to produce muscle relaxation by blocking acetylcholine receptors at the neuromuscular junction.
Moleküler Ağırlık
609,7000 g/mol
TPSA
59,00 Ų
Terapötik Alanlar
Etki Mekanizması
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.
2D Yapı
Cite this structure
Embed this structure
SMILES
C=CC[N+]1([C@H]2C[C@H]3[C@@H]4CC[C@H]5C[C@H](O)[C@@H](N6CCOCC6)C[C@]5(C)[C@H]4CC[C@]3(C)[C@H]2OC(C)=O)CCCC1.[Br-]
InChI
InChI=1S/C32H53N2O4.BrH/c1-5-14-34(15-6-7-16-34)28-20-26-24-9-8-23-19-29(36)27(33-12-17-37-18-13-33)21-32(23,4)25(24)10-11-31(26,3)30(28)38-22(2)35;/h5,23-30,36H,1,6-21H2,2-4H3;1H/q+1;/p-1/t23-,24+,25-,26-,27-,28-,29-,30-,31-,32-;/m0./s1
Molecular Formula
C32H53BrN2O4
HBD / HBA
1 / 6
Döndürülebilir Bağlar
6
Ağır Atomlar
39
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.
Sıkça Sorulan Sorular
A bromide salt form of rocuronium with the same therapeutic properties. A neuromuscular blocking agent used during surgery and intubation to produce muscle relaxation by blocking acetylcholine receptors at the neuromuscular junction.
Blocks neuromuscular transmission at the motor end plate by competing with acetylcholine for nicotinic receptor binding sites, producing skeletal muscle relaxation and paralysis.
Yes, Rocuronium 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). CHEMBL1200648. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 441351. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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