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Ketazolam

Catalog No. DB01587 Name DrugBank
CAS Number 27223-35-4 Website http://www.ualberta.ca/
M. F. C20H17ClN2O3 Telephone (780) 492-3111
M. W. 368.81358 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 1365

SYNONYMS

IUPAC name
14-chloro-4,10-dimethyl-2-phenyl-3-oxa-7,10-diazatricyclo[9.4.0.0^{2,7}]pentadeca-1(11),4,12,14-tetraene-6,9-dione
IUPAC Traditional name
ketazolam

DATABASE IDS

CAS Number 27223-35-4
PubChem SID 46507008
PubChem CID 33746

PROPERTIES

DETAILS

Description (English)
Item Information
Drug Groups approved
Description Ketazolam is a drug which is a benzodiazepine derivative. It possesses anxiolytic, anticonvulsant, sedative and skeletal muscle relaxant properties. Ketazolam is not approved for sale in the United States or Canada.
Indication Ketazolam could be used for the treatment of anxiety. In approved countries, it is indicated for the treatment of anxiety, tension, irritability and similar stress related symptoms.
Pharmacology Benzodiazepines enhance the effect of the neurotransmitter gamma-aminobutyric acid (GABA), which results in sedative, hypnotic, anxiolytic, anticonvulsant, muscle relaxant and amnesic action.
Benzodiazepines bind nonspecifically to benzodiazepine receptors which mediate sleep, affects muscle relaxation, anticonvulsant activity, motor coordination, and memory. As benzodiazepine receptors are thought to be coupled to gamma-aminobutyric acid-A (GABAA) receptors, this enhances the effects of GABA by increasing GABA affinity for the GABA receptor. Binding of GABA to the site opens the chloride channel, resulting in a hyperpolarized cell membrane that prevents further excitation of the cell.
Toxicity Symptoms of overdose include somnolence, confusion, coma, and diminished reflexes. Respiration, pulse and blood pressure should be monitored.
Biotransformation Ketazolam breaks down in the blood to diazepam which breaks down to demoxepam which breaks down to desmethyldiazepam.
Half Life 26-200 hours
Elimination Diazepam and its metabolites are excreted mainly in the urine, predominantly as their glucuronide conjugates.
External Links
Wikipedia

REFERENCES