Atracurium Besylate
Atracurium Besylate
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Atracurium Besylate

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Catalog Number PR64228815
CAS 64228-81-5
Description Atracurium besylate is the bisbenzenesulfonate salt of atracurium. It has a role as a nicotinic antagonist and a muscle relaxant. It is a quaternary ammonium salt and an organosulfonate salt.
Synonyms Atracurium besilate; Tracrium
IUPAC Name benzenesulfonate;5-[3-[1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-2-ium-2-yl]propanoyloxy]pentyl 3-[1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-2-ium-2-yl]propanoate
Molecular Weight 1243.5
Molecular Formula C65H82N2O18S2
InChI XXZSQOVSEBAPGS-UHFFFAOYSA-L
InChI Key InChI=1S/C53H72N2O12.2C6H6O3S/c1-54(22-18-38-32-48(62-7)50(64-9)34-40(38)42(54)28-36-14-16-44(58-3)46(30-36)60-5)24-20-52(56)66-26-12-11-13-27-67-53(57)21-25-55(2)23-19-39-33-49(63-8)51(65-10)35-41(39)43(55)29-37-15-17-45(59-4)47(31-37)61-6;2*7-10(8,9)6-4-2-1-3-5-6/h14-17,30-35,42-43H,11-13,18-29H2,1-10H3;2*1-5H,(H,7,8,9)/q+2;;/p-2
Associated Therapies Neuromuscular blocking therapy, Facilitation of small bowel intubation therapy
Documentation/Certification EDMF
Drug Categories Anticholinergic Agents; Benzylisoquinolines; Central Nervous System Depressants; Cholinergic Agents; Heterocyclic Compounds, Fused-Ring; Isoquinolines; Miscellaneous Skeletal Muscle Relaxants; Neuromuscular Agents; Neuromuscular Blocking Agents; Neuromuscular-Blocking Agents (Nondepolarizing); Neurotransmitter Agents; Nicotinic Antagonists; Peripheral Nervous System Agents
Drug Interactions 1,2-Benzodiazepine-The risk or severity of CNS depression can be increased when Atracurium besylate is combined with 1,2-Benzodiazepine.
Acetazolamide-The risk or severity of CNS depression can be increased when Atracurium besylate is combined with Acetazolamide.
Acetophenazine-The risk or severity of CNS depression can be increased when Atracurium besylate is combined with Acetophenazine.
Acetyldigitoxin-The risk or severity of Cardiac Arrhythmia can be increased when Atracurium besylate is combined with Acetyldigitoxin.
Aclidinium-The risk or severity of adverse effects can be increased when Atracurium besylate is combined with Aclidinium.
Half-Life The elimination half-life is approximately 20 minutes.
Isomeric SMILES C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)OC)OC)CCC(=O)OCCCCCOC(=O)CC[N+]4(CCC5=CC(=C(C=C5C4CC6=CC(=C(C=C6)OC)OC)OC)OC)C.C1=CC=C(C=C1)S(=O)(=O)[O-].C1=CC=C(C=C1)S(=O)(=O)[O-]
Type Small Molecule
Therapeutic Category Muscle Relaxant
Pharmacology

Indications

Atracurium Besylate is indicated as an adjunct to general anesthesia. It is employed to facilitate endotracheal intubation and ensure skeletal muscle relaxation during surgical procedures or mechanical ventilation.

Pharmacodynamics

Atracurium functions as a nondepolarizing skeletal muscle relaxant. Its effectiveness can be optimized by monitoring the muscle twitch response to peripheral nerve stimulation, which helps in assessing the extent of muscle relaxation. Compared to other neuromuscular blockers like d-tubocurarine, metocurine, and pancuronium, Atracurium provides a neuromuscular block with a duration approximately one-third to one-half shorter at equivalent doses. The onset of paralysis occurs more quickly and the duration of maximum effect lengthens with higher doses of Atracurium. Importantly, when maintenance doses are repeated, Atracurium does not exhibit cumulative effects on the neuromuscular blockade duration, assuming recovery is initiated before additional doses are administered. Consequently, recovery time remains consistent with repeated dosing, allowing for regular intervals of administration with predictable outcomes.

Mechanism of Action

Atracurium Besylate functions by competitively binding to cholinergic receptor sites on the motor end-plate, thereby antagonizing the action of the neurotransmitter acetylcholine. This binding process prevents acetylcholine from exerting its usual effect, resulting in neuromuscular blockade. However, this antagonism can be effectively counteracted and the neuromuscular block reversed through the administration of acetylcholinesterase inhibitors, including neostigmine, edrophonium, and pyridostigmine.

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