Laudexium metilsulfate
File:Laudexium metilsulfate.png | |
Systematic (IUPAC) name | |
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1-[(3,4-Dimethoxyphenyl)methyl]-2-[10-[1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-2-ium-2-yl]decyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-2-ium methyl sulfate
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Clinical data | |
Legal status |
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Routes of administration |
IV |
Pharmacokinetic data | |
Bioavailability | 100% (IV) |
Identifiers | |
CAS Number | 3253-60-9 ![]() |
PubChem | CID: 18618 |
ChemSpider | 17584 ![]() |
UNII | D067KDG4NU ![]() |
Synonyms | Laudolissin |
Chemical data | |
Formula | C54H80N2O16S2 |
Molecular mass | 1077.35 g/mol |
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Laudexium metilsulfate is a neuromuscular blocking drug or skeletal muscle relaxant in the category of non-depolarizing neuromuscular-blocking drugs, used adjunctively in surgical anesthesia to facilitate endotracheal intubation and to provide skeletal muscle relaxation during surgery or mechanical ventilation.
Laudexium[1] is no longer used in clinical practice, though it was introduced clinically in the early 1950s.[citation needed] It has about half the potency, a slower onset of action and a duration of action much longer than that of d-tubocurarine.[2] As with all clinically established (as well as experimental agents) with a non-depolarizing mechanism of action, its pharmacological action can be antagonized by anticholinesterases.
The displacement of laudexium from clinical use was assured owing to recurrent reports of significant post-operative re-curarization.[3]
References
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External links
- Neuromuscular blocking agents at the US National Library of Medicine Medical Subject Headings (MeSH)
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- Quaternary ammonium compounds
- Tetrahydroisoquinolines
- Phenol ethers