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Temazepam

产品号 DB00231 公司名称 DrugBank
CAS号 846-50-4 公司网站 http://www.ualberta.ca/
分子式 C16H13ClN2O2 电 话 (780) 492-3111
分子量 300.73962 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 116

产品价格信息

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产品别名

标题
Temazepam
IUPAC标准名
7-chloro-3-hydroxy-1-methyl-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepin-2-one
IUPAC传统名
temazepam
商标名
Euhypnos
Euipnos
Levanzene
Crisonar
Cerepax
Temaz
Gelthix
Levanxene
Levanxol
Mabertin
Normison
Perdorm
Remestan
Restoril
Apo-Temazepam
Novo-Temazepam
Planum
Signopam
别名
Methyloxazepam
Hydroxydiazepam
Oxydiazepam
N-Methyloxazepam

产品登记号

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

产品性质

疏水性(logP) 3
溶解度 164 mg/L

产品详细信息

详细说明 (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

参考文献

  • 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