Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Mexazolam

From Wikipedia, the free encyclopedia
Benzodiazepam
Pharmaceutical compound
Mexazolam
Clinical data
Trade namesMelex, Sedoxil
Other names13-chloro- 2-(2-chlorophenyl)- 5-methyl- 3-oxa- 6,9-diazatricyclo[8.4.0.02,6] tetradeca- 1(10),11,13-trien- 8-one
AHFS/Drugs.comInternational Drug Names
Routes of
administration
Oral
ATC code
Legal status
Legal status
Pharmacokinetic data
MetabolismLiver (CYP3A4)
ExcretionKidney
Identifiers
  • 10-chloro-11b-(2-chlorophenyl)-3-methyl-2,3,5,7-tetrahydro-[1,3]oxazolo[3,2-d][1,4]benzodiazepin-6-one
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC18H16Cl2N2O2
Molar mass363.24 g·mol−1
3D model (JSmol)
  • Clc1ccccc1C42OCC(N2CC(=O)Nc3c4cc(Cl)cc3)C
  • InChI=1S/C18H16Cl2N2O2/c1-11-10-24-18(13-4-2-3-5-15(13)20)14-8-12(19)6-7-16(14)21-17(23)9-22(11)18/h2-8,11H,9-10H2,1H3,(H,21,23) checkY
  • Key:ANUCDXCTICZJRH-UHFFFAOYSA-N checkY
  (verify)

Mexazolam[1] (marketed under the trade namesMelex andSedoxil)[2] is a drug which is abenzodiazepine derivative.[3] Mexazolam has been trialed for anxiety and was found to be effective in alleviating anxiety at one week follow-up. Mexazolam is metabolised via theCYP3A4 pathway.HMG-CoA reductase inhibitors includingsimvastatin,simvastatin acid,lovastatin,fluvastatin,atorvastatin andcerivastatin inhibit the metabolism of mexazolam,[4] but not the HMG-CoA reductase inhibitorpravastatin.[5][6] Its principal active metabolites are chlorodesmethyldiazepam (also known as chloronordiazepam ordelorazepam, trade name Dadumir) and chloroxazepam (also known aslorazepam, trade name Ativan).[7]

See also

[edit]

References

[edit]
  1. ^DE Patent 1954065
  2. ^"Benzodiazepine Names". non-benzodiazepines.org.uk. Archived fromthe original on 2008-12-08. Retrieved2009-04-05.
  3. ^Kurono Y, Kamiya K, Kuwayama T, Jinno Y, Yashiro T, Ikeda K (September 1987)."Kinetics and mechanism of the acid-base equilibrium of mexazolam and comparison with those of other commercial benzodiazepinooxazole drugs".Chemical & Pharmaceutical Bulletin.35 (9):3831–3837.doi:10.1248/cpb.35.3831.PMID 2893667.
  4. ^Mc Donnell CG, Harte S, O'Driscoll J, O'Loughlin C, Van Pelt FN, Shorten GD (September 2003)."The effects of concurrent atorvastatin therapy on the pharmacokinetics of intravenous midazolam".Anaesthesia.58 (9):899–904.doi:10.1046/j.1365-2044.2003.03339.x.PMID 12911366.S2CID 25382546.
  5. ^Ishigami M, Takasaki W, Ikeda T, Komai T, Ito K, Sugiyama Y (August 2002). "Sex difference in inhibition of in vitro mexazolam metabolism by various 3-hydroxy-3-methylglutaryl-coenzyme a reductase inhibitors in rat liver microsomes".Drug Metabolism and Disposition.30 (8):904–910.doi:10.1124/dmd.30.8.904.PMID 12124308.S2CID 2620104.
  6. ^Ishigami M, Honda T, Takasaki W, Ikeda T, Komai T, Ito K, Sugiyama Y (March 2001)."A comparison of the effects of 3-hydroxy-3-methylglutaryl-coenzyme a (HMG-CoA) reductase inhibitors on the CYP3A4-dependent oxidation of mexazolam in vitro".Drug Metabolism and Disposition.29 (3):282–288.PMID 11181496.
  7. ^Fernandes H, Moreira R (June 2014)."Mexazolam: clinical efficacy and tolerability in the treatment of anxiety".Neurology and Therapy.3 (1):1–14.doi:10.1007/s40120-014-0016-7.PMC 4381915.PMID 26000220.
1,4-Benzodiazepines
1,5-Benzodiazepines
2,3-Benzodiazepines*
Triazolobenzodiazepines
Imidazobenzodiazepines
Oxazolobenzodiazepines
Thienodiazepines
Thienotriazolodiazepines
Thienobenzodiazepines*
Pyridodiazepines
Pyridotriazolodiazepines
Pyrazolodiazepines
Pyrrolodiazepines
Tetrahydroisoquinobenzodiazepines
Pyrrolobenzodiazepines*
Benzodiazepine prodrugs
* atypical activity profile (notGABAA receptor ligands)
Alcohols
Barbiturates
Benzodiazepines
Carbamates
Flavonoids
Imidazoles
Kava constituents
Monoureides
Neuroactive steroids
Nonbenzodiazepines
Phenols
Piperidinediones
Pyrazolopyridines
Quinazolinones
Volatiles/gases
Others/unsorted
Stub icon

Thissedative-related article is astub. You can help Wikipedia byexpanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Mexazolam&oldid=1244803878"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp