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Halothane

Catalog No. DB01159 Name DrugBank
CAS Number 151-67-7 Website http://www.ualberta.ca/
M. F. C2HBrClF3 Telephone (780) 492-3111
M. W. 197.3815496 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 1030

SYNONYMS

IUPAC name
2-bromo-2-chloro-1,1,1-trifluoroethane
IUPAC Traditional name
halothane
Brand Name
Narkotan
Fluktan
Halsan
Narcotan
Narcotane
Phthorothanum
Halothane
Anestan
Chalothane
Halan
Halotan
Rhodialothan
Fluothane
Synonyms
Fluorotane
Fluorothane
Ftorotan [Russian]
Halothanum [INN-Latin]
Alotano [Dcit]
Bromchlortrifluoraethanum
Ftuorotan
Halotano [INN-Spanish]
2-Bromo-2-Chloro-1,1,1-Trifluoroethane
Bromochlorotrifluoroethane
Cf3chclbr
Freon 123b1
Halothan
Narcotann Ne-Spofa [Russian]

DATABASE IDS

PubChem SID 46506589
PubChem CID 3562
CAS Number 151-67-7

PROPERTIES

Hydrophobicity(logP) 2.7
Solubility 3.45 mg/ml

DETAILS

Description (English)
Item Information
Drug Groups approved
Description A nonflammable, halogenated, hydrocarbon anesthetic that provides relatively rapid induction with little or no excitement. Analgesia may not be adequate. nitrous oxide is often given concomitantly. Because halothane may not produce sufficient muscle relaxation, supplemental neuromuscular blocking agents may be required. (From AMA Drug Evaluations Annual, 1994, p178)
Indication For the induction and maintenance of general anesthesia
Pharmacology Halothane is a general inhalation anesthetic used for induction and maintenance of general anesthesia. It reduces the blood pressure and frequently decreases the pulse rate and depresses respiration. It induces muscle relaxation and reduces pains sensitivity by altering tissue excitability. It does so by decreasing the extent of gap junction mediated cell-cell coupling and altering the activity of the channels that underlie the action potential.
Toxicity Toxic effects of halothane include malignant hyperthermia and hepatitis.
Affected Organisms
Humans and other mammals
Biotransformation Halothane is metabolized in the liver, primarily by CYP2E1, and to a lesser extent by CYP3A4 and CYP2A6.
References
Bovill JG: Inhalation anaesthesia: from diethyl ether to xenon. Handb Exp Pharmacol. 2008;(182):121-42. [Pubmed]
External Links
Wikipedia
RxList

REFERENCES

  • Bovill JG: Inhalation anaesthesia: from diethyl ether to xenon. Handb Exp Pharmacol. 2008;(182):121-42. Pubmed