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106819-53-8

106819-53-8 Structure

106819-53-8 Structure
IdentificationBack Directory
[Name]

DOXACURIUM CHLORIDE
[CAS]

106819-53-8
[Synonyms]

Nuromax
BW-A938U
Doxacurium
DOXACURIUM CHLORIDE
bis[3-[6,7,8-trimethoxy-2-methyl-1-[(3,4,5-trimethoxyphenyl)methyl]-3,4-dihydro-1h-isoquinolin-2-ium-2-yl]propyl] butanedioate dichloride
[Molecular Formula]

C56H78Cl2N2O16
[MDL Number]

MFCD00906167
[MOL File]

106819-53-8.mol
[Molecular Weight]

1106.13
Raw materials And Preparation ProductsBack Directory
[Raw materials]

SUCCINYL CHLORIDE-->PAPAVERINE HYDROCHLORIDE-->DoxacuriumChloride-->3-Iodopropanol
Hazard InformationBack Directory
[Description]

Doxacurium chloride is an injectable, noncumulative, nondepolarizing neuromuscular blocking agent which exhibits no significant cardiovascular effects. It is a mixture of (lR, l′S, 2S, 2′R), (lR, l′R, 2S, 2′s) and (lS, l′S, 2R, 2′R) isomers of a bis-benzylisoquinolinium diester.Doxacurium chloride provides satisfactory intubation with duration of action similar to d-tubocurarine or pancuronium. However, it is reported to be 2 to 3 times as potent as pancuronium.
[Originator]

Wellcome (United Kingdom)
[Uses]

Neuromuscular blocking agent.
[Brand name]

Nuromax (Abbott).
[General Description]

The molecular structure of doxacuriumchloride, 1,2,3,4-tetrahydro-2-(3-hydroxypropyl)-6,7,8-trimethoxy2-methyl-1-(3,4,5-trimethoxybenzyl) isoquinoliniumchloride succinate (Nuromax), provides thepossibility for 10 stereoisomers: 4 d,l pairs and two mesoforms. Of the 10 stereoisomers, 3 are all-trans configuration,and these are the only active ones. Doxacurium chlorideis a long-acting nondepolarizing blocking agent. The drugdiffers from drugs such as gallium and pancuronium in thatit has no vagolytic activity. It is used as a skeletal musclerelaxant in surgical procedures expected to last longer than90 minutes.
[Pharmacokinetics]

Doxacurium is a mixture of three trans, trans-stereoisomers, a dl pair [(1R,1′R,2S,2′S) and (1S,1′S,2R,2′R)] and a meso form (1R,1′S,2S,2′R). Doxacurium is hydrophilic, has a small volume of distribution, and is distributed primarily to extracellular fluids. It is not metabolized by plasma cholinesterase or hepatic enzymes and does not undergo Hofmann elimination.
Questions And AnswerBack Directory
[Reaction]

Ligand for the palladium catalyzed aqueous Lipshutz-Negishi cross-coupling of alkyl halides with aryl electrophiles. Reactions of 106819-53-8
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