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Decamethonium

From Wikipedia, the free encyclopedia
Medication
Pharmaceutical compound
Decamethonium
Clinical data
ATC code
  • None
Identifiers
  • Trimethyl-(10-trimethylammoniodecyl)ammonium
CAS Number
PubChemCID
DrugBank
ChemSpider
UNII
ChEBI
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC16H38N2
Molar mass258.494 g·mol−1
3D model (JSmol)
  • [Br-].[Br-].C(CCCC[N+](C)(C)C)CCCCC[N+](C)(C)C
  • InChI=1S/C16H38N2.2BrH/c1-17(2,3)15-13-11-9-7-8-10-12-14-16-18(4,5)6;;/h7-16H2,1-6H3;2*1H/q+2;;/p-2 checkY
  • Key:HLXQFVXURMXRPU-UHFFFAOYSA-L checkY
 ☒NcheckY (what is this?)  (verify)

Decamethonium (Syncurine) is adepolarizingmuscle relaxant or neuromuscular blocking agent,[1] and is used inanesthesia to induceparalysis.

Pharmacology

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Decamethonium, which has a short action time, is similar toacetylcholine and acts as a partialagonist of thenicotinic acetylcholine receptor. In themotor endplate, it causesdepolarization, preventing further effects to the normal release ofacetylcholine from thepresynaptic terminal, and therefore preventing the neural stimulus from affecting themuscle. In the process of binding, decamethonium activates (depolarizes) the motor endplate - but since the decamethonium itself is not degraded, the membrane remains depolarized and unresponsive to normal acetylcholine release.

Contraindications/limitations

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Decamethonium does not produce unconsciousness or anesthesia, and its effects may cause considerable psychological distress while simultaneously making it impossible for a patient to communicate. For these reasons, administration of the drug to a conscious patient is strongly advised against, except in necessary emergency situations.

Decamethonium was used clinically in the UK for many years, but it is now available only for research purposes.[citation needed]

See also

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References

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  1. ^Lee C, Jones T (May 2002)."Molecular conformation-activity relationship of decamethonium congeners".British Journal of Anaesthesia.88 (5):692–9.doi:10.1093/bja/88.5.692.PMID 12067008.
Peripherally acting
(primarilyantinicotinic,
NMJ block)
Non-depolarizing
Curarealkaloids
4° ammonium agents
Depolarizing
ACh release inhibitors
Centrally acting
Carbamic acid esters
Benzodiazepines
Nonbenzodiazepines
Thienodiazepines
Quinazolines
Anticholinergics
(Antimuscarinics)
Other
Directly acting
nAChRsTooltip Nicotinic acetylcholine receptors
Agonists
(andPAMsTooltip positive allosteric modulators)
Antagonists
(andNAMsTooltip negative allosteric modulators)
Precursors
(andprodrugs)
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