Substance
ID:710
Names and Identifiers
IUPAC name
7-chloro-1-methyl-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepin-2-one
IUPAC Traditional name
diazepam
Synonyms
DiazepamDAPMethyldiazepinone
Brand Name
TranqdynTranquo-PurenUnisedilUsempax ApPro-PamQ-Pam RelaniumSarometSerenaminStesolidStesolinDiastatDiazepanDomaliumKabivitrumMorosanNoanApozepamBensedinBialzepamCeregulartConditionDiapamTranquiritValreleaseVeliumAlboralAmiprolSeduksenSerenackSetonilSibazonSolisSonaconPaceumPacitranPaxateQuetinilRelaminalSedapamDuxenFaustanFrustanGewacalmGihitanMandrozepAnsiolinApaurinAtensineCalmposeDiacepanDizacUmbriumValeoVivolZipanParantenPlidanSeduxenTensopamTranimulTranquo-TablinenLembrolLeviumLiberetasNeurolytrilNovazamNovo-DipamDiazemulsDiazepam IntensolDiazetardDuksenE-PamEvacalmVivalZetranApo-DiazepamArmonilDialagDialarTranquaseValaxonaValiquidValitranValiumVatranRenborinRuhsitusSedipamSerenzinServizepamSibazonePaxelPms-DiazepamQ-PamQuiatrilQuievitaRelaniumFaustan,FreudalKiatriumLA IIILa-IiiLamraDiazemulusDienpaxDipamDipezonaEridanEurosanAn-DingAnsiolisinaAssivalAtilenCalmociteneCercineAliseumAlupram
Properties
Physical Property
Solubility
Slightly soluble (50 mg/L)
Hydrophobicity(logP)
2.9
Molecule Details
Drug Groups
illicit; approved
Description
A benzodiazepine with anticonvulsant, anxiolytic, sedative, muscle relaxant, and amnesic properties and a long duration of action. Its actions are mediated by enhancement of gamma-aminobutyric acid activity. It is used in the treatment of severe anxiety disorders, as a hypnotic in the short-term management of insomnia, as a sedative and premedicant, as an anticonvulsant, and in the management of alcohol withdrawal syndrome. (From Martindale, The Extra Pharmacopoeia, 30th ed, p589)
Indication
Used in the treatment of severe anxiety disorders, as a hypnotic in the short-term management of insomnia, as a sedative and premedicant, as an anticonvulsant, and in the management of alcohol withdrawal syndrome.
Pharmacology
Diazepam, a benzodiazepine, generates the same active metabolite as chlordiazepoxide and clorazepate. In animals, diazepam appears to act on parts of the limbic system, the thalamus and hypothalamus, and induces calming effects. Diazepam, unlike chlorpromazine and reserpine, has no demonstrable peripheral autonomic blocking action, nor does it produce extrapyramidal side effects; however, animals treated with diazepam do have a transient ataxia at higher doses. Diazepam was found to have transient cardiovascular depressor effects in dogs. Long-term experiments in rats revealed no disturbances of endocrine function. Injections into animals have produced localized irritation of tissue surrounding injection sites and some thickening of veins after intravenous use.
Toxicity
Symptoms of overdose include somnolence, confusion, coma, and diminished reflexes. Respiration, pulse and blood pressure should be monitored.
Affected Organisms
Humans and other mammals
Biotransformation
Hepatic via the Cytochrome P450 enzyme system. The main active metabolite is desmethyldiazepam, in addition to minor active metabolites including temazepam and oxazepam.
Absorption
Essentially complete, with a bioavailability of 93%.
Half Life
Biphasic 1-2 days and 2-5 days, active metabolites with long half lives.
Protein Binding
98.5%
Elimination
Diazepam and its metabolites are excreted mainly in the urine, predominantly as their glucuronide conjugates.
Distribution
* 0.8 to 1.0 L/kg [young healthy males]
Clearance
* 20-30 mL/min
References
•
Mant A, Whicker SD, McManus P, Birkett DJ, Edmonds D, Dumbrell D: Benzodiazepine utilisation in Australia: report from a new pharmacoepidemiological database. Aust J Public Health. 1993 Dec;17(4):345-9.
[Pubmed]
•
Earley JV, Fryer RI, Ning RY: Quinazolines and 1,4-benzodiazepines. LXXXIX: Haptens useful in benzodiazepine immunoassay development. J Pharm Sci. 1979 Jul;68(7):845-50.
[Pubmed]
•
Usami N, Yamamoto T, Shintani S, Ishikura S, Higaki Y, Katagiri Y, Hara A: Substrate specificity of human 3(20)alpha-hydroxysteroid dehydrogenase for neurosteroids and its inhibition by benzodiazepines. Biol Pharm Bull. 2002 Apr;25(4):441-5.
[Pubmed]
•
Oishi R, Nishibori M, Itoh Y, Saeki K: Diazepam-induced decrease in histamine turnover in mouse brain. Eur J Pharmacol. 1986 May 27;124(3):337-42.
[Pubmed]
•
McLean MJ, Macdonald RL: Benzodiazepines, but not beta carbolines, limit high frequency repetitive firing of action potentials of spinal cord neurons in cell culture. J Pharmacol Exp Ther. 1988 Feb;244(2):789-95.
[Pubmed]
External Links
Molecular Spectra
No Data Available
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References
• Mant A, Whicker SD, McManus P, Birkett DJ, Edmonds D, Dumbrell D: Benzodiazepine utilisation in Australia: report from a new pharmacoepidemiological database. Aust J Public Health. 1993 Dec;17(4):345-9. Pubmed
• McLean MJ, Macdonald RL: Benzodiazepines, but not beta carbolines, limit high frequency repetitive firing of action potentials of spinal cord neurons in cell culture. J Pharmacol Exp Ther. 1988 Feb;244(2):789-95. Pubmed
• Usami N, Yamamoto T, Shintani S, Ishikura S, Higaki Y, Katagiri Y, Hara A: Substrate specificity of human 3(20)alpha-hydroxysteroid dehydrogenase for neurosteroids and its inhibition by benzodiazepines. Biol Pharm Bull. 2002 Apr;25(4):441-5. Pubmed
• Earley JV, Fryer RI, Ning RY: Quinazolines and 1,4-benzodiazepines. LXXXIX: Haptens useful in benzodiazepine immunoassay development. J Pharm Sci. 1979 Jul;68(7):845-50. Pubmed
• Oishi R, Nishibori M, Itoh Y, Saeki K: Diazepam-induced decrease in histamine turnover in mouse brain. Eur J Pharmacol. 1986 May 27;124(3):337-42. Pubmed