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Temazepam

Catalog No. DB00231 Name DrugBank
CAS Number 846-50-4 Website http://www.ualberta.ca/
M. F. C16H13ClN2O2 Telephone (780) 492-3111
M. W. 300.73962 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 116

SYNONYMS

IUPAC name
7-chloro-3-hydroxy-1-methyl-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepin-2-one
IUPAC Traditional name
temazepam
Brand Name
Euhypnos
Euipnos
Levanzene
Crisonar
Cerepax
Temaz
Gelthix
Levanxene
Levanxol
Mabertin
Normison
Perdorm
Remestan
Restoril
Apo-Temazepam
Novo-Temazepam
Planum
Signopam
Synonyms
Methyloxazepam
Hydroxydiazepam
Oxydiazepam
N-Methyloxazepam

DATABASE IDS

PubChem SID 46506604
CAS Number 846-50-4
PubChem CID 5391

PROPERTIES

Hydrophobicity(logP) 3
Solubility 164 mg/L

DETAILS

Description (English)
Item Information
Drug Groups approved
Description A benzodiazepine that acts as a gamma-aminobutyric acid modulator and anti-anxiety agent. [PubChem]
Indication For the short-term treatment of insomnia (generally 7-10 days).
Pharmacology Temazepam is a benzodiazepine used as a hypnotic agent in the management of insomnia. Temazepam produces CNS depression at limbic, thalamic, and hypothalamic levels of the CNS. Temazepam increases the affinity of the neurotransmitter gamma-aminobutyric acid (GABA) for GABA receptors by binding to benzodiazepine receptors. Results are sedation, hypnosis, skeletal muscle relaxation, anticonvulsant activity, and anxiolytic action.
Affected Organisms
Humans and other mammals
Biotransformation Hepatic. Temazepam is completely metabolized through conjugation prior to excretion. The major metabolite is the O-conjugate of temazepam (90%).
Absorption Well absorbed, minimal first-pass metabolism.
Half Life 10-20 hours
Protein Binding 96%
Elimination Temazepam was completely metabolized through conjugation prior to excretion; 80% to 90% of the dose appeared in the urine.
References
Rickels K: The clinical use of hypnotics: indications for use and the need for a variety of hypnotics. Acta Psychiatr Scand Suppl. 1986;332:132-41. [Pubmed]
Oelschlager H: [Chemical and pharmacologic aspects of benzodiazepines] Schweiz Rundsch Med Prax. 1989 Jul 4;78(27-28):766-72. [Pubmed]
Vozeh S: [Pharmacokinetic of benzodiazepines in old age] Schweiz Med Wochenschr. 1981 Nov 21;111(47):1789-93. [Pubmed]
Shats V, Kozacov S: [Falls in the geriatric department: responsibility of the care-giver and the hospital] Harefuah. 1995 Jun 1;128(11):690-3, 743. [Pubmed]
Rooke KC: The use of flurazepam (dalmane) as a substitute for barbiturates and methaqualone/diphenhydramine (mandrax) in general practice. J Int Med Res. 1976;4(5):355-9. [Pubmed]
External Links
Wikipedia
RxList
PDRhealth
Drugs.com

REFERENCES

  • Rickels K: The clinical use of hypnotics: indications for use and the need for a variety of hypnotics. Acta Psychiatr Scand Suppl. 1986;332:132-41. Pubmed
  • Oelschlager H: [Chemical and pharmacologic aspects of benzodiazepines] Schweiz Rundsch Med Prax. 1989 Jul 4;78(27-28):766-72. Pubmed
  • Vozeh S: [Pharmacokinetic of benzodiazepines in old age] Schweiz Med Wochenschr. 1981 Nov 21;111(47):1789-93. Pubmed
  • Shats V, Kozacov S: [Falls in the geriatric department: responsibility of the care-giver and the hospital] Harefuah. 1995 Jun 1;128(11):690-3, 743. Pubmed
  • Rooke KC: The use of flurazepam (dalmane) as a substitute for barbiturates and methaqualone/diphenhydramine (mandrax) in general practice. J Int Med Res. 1976;4(5):355-9. Pubmed