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Vecuronium (bromide)

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    Vecuronium (bromide)
  • Vecuronium (bromide)
Cat No: 15603
Biochemicals - Receptor Pharmacology
Cayman

Vecuronium is a non-depolarizing muscle relaxant derived from the aminosteroid pancuronium (Item No. 23778) and used adjunctively to general anesthesia.{25532} It competitively blocks cholinergic receptors at the motor end plate of the neuromuscular j...

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This product can only be bought through Cayman Chemical. Please contact us.

Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 1-[(2?,3?,5?,16?,17?)-3,17-bis(acetyloxy)-2-(1-piperidinyl)androstan-16-yl]-1-methyl-piperidinium, monobromide
Correlated keywords:
  • 86029-43-8 63884-?29-?7 72254-?12-?7 74531-?67-?2 ORG NC45 Norcuron nondepolarizing muscles relaxant pancuronium anesthesia cholinergic receptors blockers neuromuscular junctions paralysis bromides non-depolarizing non depolarizing musculax norcuron NCs NC45 NC-45 45 twitch tensions Org-NC 45 Musculax Androstane piperidinium deriv derivatives NC
Product Overview:
Vecuronium is a non-depolarizing muscle relaxant derived from the aminosteroid pancuronium (Item No. 23778) and used adjunctively to general anesthesia.{25532} It competitively blocks cholinergic receptors at the motor end plate of the neuromuscular junction, inducing temporary paralysis.{25531} In humans, it has been shown to reduce muscle twitch tension with an ED50 value of 0.15 mg/kg for a duration of 27 minutes without inducing cardiovascular effects.{25532}
Size 10 mg
Shipping room temp.
CAS Number 50700-72-6
Molecular Formula C34H57N2O4 • Br
SMILES C[C@@]12[C@](C[C@H]([N+]3(C)CCCCC3)[C@@H]2OC(C)=O)([H])[C@]4([H])CC[C@@]5([H])C[C@H](OC(C)=O)[C@@H](N6CCCCC6)C[C@]5(C)[C@@]4([H])CC1.[Br-]
Molecular Weight 637,7
Formulation A solid
Purity ≥98%
Custom Code 2933.39
UNSPSC code 12352100

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Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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