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QuickView for Pancuronium (compound)


PubChem
Name: Pancuronium
PubChem Compound ID: 27350
Description: A bis-quaternary steroid that is a competitive nicotinic antagonist. As a neuromuscular blocking agent it is more potent than CURARE but has less effect on the circulatory system and on histamine release.
Molecular formula: C35H60Br2N2O4
Molecular weight: 732.67 g/mol
Synonyms:
Bromure de pancuronium [INN-French]; Piperidinium, 1,1'-((2beta,3alpha,5alpha,16beta,17beta)-3,17-bis(acetyloxy)androstane-2,16-diyl)bis(1-methyl)-, dibromide; 1,1'-(3alpha,17beta-Bis(acetyloxy)-5alpha-androstane-2beta,16beta-diyl)bis(1-methylpiperidinium) dibromide; NA 97; Piperidinium, 1,1'-(2-beta,16-beta-(3-alpha,17-beta-dihydroxy-5-alpha-androstanylene))bis(1-methyl-, dibromide, diacetate; 3alpha,17beta-Diacetoxy-2beta,16beta-dipiperidino-5alpha-androstane dimethobromide; Org NA 97; Pancuronium bromide [USAN:BAN:INN:JAN]; Pancuronium bromide (JP15/USAN); D00492.
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DrugBank
Identification
Name: Pancuronium
Name (isomeric): DB01337
Drug Type: small molecule
Description: A bis-quaternary steroid that is a competitive nicotinic antagonist. As a neuromuscular blocking agent it is more potent than CURARE but has less effect on the circulatory system and on histamine release.
Synonyms:
Pancuronium dibromide; Bromure de pancuronium [inn-french]; Pancuronium bromide; Bromuro de pancuronio [inn-spanish]
Brand: Mioblock, Pavulon
Category: Neuromuscular Nondepolarizing Agents, Nicotinic Antagonists
CAS number: 15500-66-0
Pharmacology
Indication: Used as a muscle relaxant during anesthesia and surgical procedures.
Pharmacology:
Pancuronium is a typical non-depolarising curare-mimetic muscle relaxant. It acts as a competitive acetylcholine antagonist on neuromuscular junctions, displacing acetylcholine (hence competitive) from its post-synaptic nicotinic acetylcholine receptors. It is, unlike suxamethonium, a non-depolarising agent, which means, that it causes no spontaneo...
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Mechanism of Action: Nondepolarizing neuromuscular blocking agents inhibit neuromuscular transmission by competing with acetylcholine for the cholinergic receptors of the motor end plate, thereby reducing the response of the end plate to acetylcholine. This type of neuromuscular block is usually antagonized by anticholinesterase agents.
Protein binding: 77 to 91%
Biotransformation: Hepatic.
Half Life: 1.5 to 2.7 hours.
Clearance: Plasma cl=1.1–1.9 mL/minute/kg
Affected organisms: Humans and other mammals
Interactions
Drug interaction:
TobramycinThe agent increases the effect of the muscle relaxant
QuinineThe quinine derivative increases the effect of the muscle relaxant
AzathioprineThe agent decreases the effect of the muscle relaxant
PhenytoinPhenytoin decreases the effect of the muscle relaxant
AminophyllineTheophylline decreases the effect of muscle relaxant
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