Home > Compound List > Product Information
Temazepam_Molecular_structure_CAS_846-50-4)
Click picture or here to close

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