Substance

ID:177

Names and Identifiers
IUPAC name
ethyl 1-(1-phenylethyl)-1H-imidazole-5-carboxylate
Synonyms
EtomidateEtomidic acid
IUPAC Traditional name
etomidate
Brand Name
HypnomidateAmidate
Registration numbers
CAS Number
Properties
Physical Property
Hydrophobicity(logP)
2.9
Solubility
63.2 mg/L
Molecule Details
Drug Groups
approved
Description
Imidazole derivative anesthetic and hypnotic with little effect on blood gases, ventilation, or the cardiovascular system. It has been proposed as an induction anesthetic. [PubChem]
Indication
Used in the induction of general anesthesia.
Pharmacology
Etomidate is a non-barbiturate hypnotic that acts at the level of the reticular-activating system to produce anesthesia. Etomidate is an imidazole compound that appears to depress CNS function via GABA. Duration of action is intermediate between thiopental and methohexital, and recovery from a single dose is rapid with little residual depression. Like the barbiturates and propofol, etomidate is does not induce analgesia. Etomidate induces unconsciousness within one circulation time. Recovery is rapid as a result of extensive redistribution and rapid metabolism.
Toxicity
Undesirable side effects of etomidate that may limit its use include pain on injection, myoclonus and adrenocortical suppression lasting 4-6 hours following an induction dose.
Affected Organisms
Humans and other mammals
Biotransformation
Hepatic. Metabolized rapidly by ester hydrolysis to inactive metabolites.
Half Life
75 minutes.
Protein Binding
76%, primarily to serum albumin.
Elimination
Approximately 75% of the administered dose is excreted in the urine during the first day after injection.
External Links
Molecular Spectra
No Data Available
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References
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