Pancuronium Bromide

CHEMBL1200757 Phase 4 Approved Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
732.7 g/mol
LogP
Phase
4

Temporary paralysis of skeletal muscle is the intended effect of pancuronium bromide, used during surgery and to facilitate mechanical ventilation. The agent acts at the neuromuscular junction, blocking transmission between motor nerve and muscle fibre so that contraction cannot occur; consciousness and sensation are unaffected, which is why it is given only alongside anaesthesia and sedation. Because ventilation itself depends on skeletal muscle, use is restricted to settings where the airway is controlled and respiration supported. The bromide salt carries the therapeutic properties of pancuronium without modification. Chemically the salt is C35H60Br2N2O4 with a mass near 732.7 g/mol, approved and developed through the final clinical phase.

A bromide salt form of pancuronium with the same therapeutic properties. This muscle relaxant is used during surgery or mechanical ventilation to temporarily paralyze muscles.

Molecular Weight

732.7000 g/mol

TPSA

52.60 Ų

Therapeutic Areas

Mechanism of Action

A long-acting non-depolarising neuromuscular blocking agent. Pancuronium competes with acetylcholine for nicotinic receptors at the motor end plate, preventing depolarisation and producing flaccid skeletal muscle paralysis that is reversed by acetylcholinesterase inhibitors such as neostigmine. Vagolytic and sympathomimetic activity accounts for the rise in heart rate seen after dosing.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanism

A long-acting non-depolarising neuromuscular blocking agent. Pancuronium competes with acetylcholine for nicotinic receptors at the motor end plate, preventing depolarisation and producing flaccid skeletal muscle paralysis that is reversed by …

2D Structure

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SMILES

CC(=O)O[C@H]1C[C@@H]2CC[C@@H]3[C@H](CC[C@@]4(C)[C@H]3C[C@H]([N+]3(C)CCCCC3)[C@@H]4OC(C)=O)[C@@]2(C)C[C@@H]1[N+]1(C)CCCCC1.[Br-].[Br-]

InChI

InChI=1S/C35H60N2O4.2BrH/c1-24(38)40-32-21-26-13-14-27-28(35(26,4)23-31(32)37(6)19-11-8-12-20-37)15-16-34(3)29(27)22-30(33(34)41-25(2)39)36(5)17-9-7-10-18-36;;/h26-33H,7-23H2,1-6H3;2*1H/q+2;;/p-2/t26-,27+,28-,29-,30-,31-,32-,33-,34-,35-;;/m0../s1

Molecular Formula

C35H60Br2N2O4

HBD / HBA

- / 6

Rotatable Bonds

6

Heavy Atoms

43

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.

Frequently Asked Questions

A bromide salt form of pancuronium with the same therapeutic properties. This muscle relaxant is used during surgery or mechanical ventilation to temporarily paralyze muscles.

A long-acting non-depolarising neuromuscular blocking agent. Pancuronium competes with acetylcholine for nicotinic receptors at the motor end plate, preventing depolarisation and producing flaccid skeletal muscle paralysis that is reversed by acetylcholinesterase inhibitors such as neostigmine. Vagolytic and sympathomimetic activity accounts for the rise in heart rate seen after dosing.

Yes, Pancuronium Bromide 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). CHEMBL1200757. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 27350. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-08-20.

Medical Disclaimer

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.