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Contents

   



(Top)
  


1 Legal status  




2 See also  




3 References  













Metizolam






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From Wikipedia, the free encyclopedia
  

Metizolam
Clinical data
Dependence
liability		Moderate
Routes of
administration		Oral, sublingual, rectal
Legal status
Legal status
  • CA: Unscheduled
  • DE: NpSG (Industrial and scientific use only)
  • UK: Under Psychoactive Substances Act
  • Illegal in Sweden
    • Identifiers

    • 4-(2-Chlorophenyl)-2-ethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine

    CAS Number
    PubChem CID
    ChemSpider
    UNII
    ChEMBL
    CompTox Dashboard (EPA)
    Chemical and physical data
    FormulaC16H13ClN4S
    Molar mass328.82 g·mol−1
    3D model (JSmol)

    • ClC1=C(C=CC=C1)C3=NCC2=NN=C[N]2C4=C3C=C(S4)CC

    • InChI=1S/C16H13ClN4S/c1-2-10-7-12-15(11-5-3-4-6-13(11)17)18-8-14-20-19-9-21(14)16(12)22-10/h3-7,9H,2,8H2,1H3

    • Key:NQSSWDKQLVBUQN-UHFFFAOYSA-N

    Metizolam (also known as desmethyletizolam) is a thienotriazolodiazepine that is the demethylated analogue of the closely related etizolam.[1][2][3][4][5][6]

    [edit]

    Following its sale as a designer drug,[7] metizolam was classified as controlled substance in Sweden on 26. January 2016.[8]

    See also

    [edit]

    References

    [edit]
    1. ^ Weber K, Bauer A, Langbein A, Daniel H (20 September 1978). "Heteroaromaten mit anellierten Siebenringen, III. Umwandlung von Thienotriazolooxazepinen in Diazepine". Justus Liebigs Annalen der Chemie (in German). 1978 (8): 1257–1265. doi:10.1002/jlac.197819780806. ISSN 1099-0690.
  • ^ US 3904641, Nakanishi M, Tahara T, Araki K, Shiroki M, "Triazolothienodiazepine compounds", issued 9 September 1975, assigned to Welfide Corp 
  • ^ EP 0776892, Hiroshi K, Ehara Syuji E, Hideaki S, Moriwaki Minoru M, Kenichi O, "Thienylazole compound and thienotriazolodiazepine compound", published 1997-06-04, assigned to Yoshitomi Pharmaceutical Industries, Ltd. 
  • ^ EP 0315698, Moriwaki M, Abe M, Mikashima H, Tahara T, "Thieno(triazolo)diazepine compounds and medicinal application of the same", published 1993-03-03, assigned to Yoshitomi Pharmaceutical Industries, Ltd. 
  • ^ Moosmann B, Bisel P, Franz F, Huppertz LM, Auwärter V (November 2016). "Characterization and in vitro phase I microsomal metabolism of designer benzodiazepines - an update comprising adinazolam, cloniprazepam, fonazepam, 3-hydroxyphenazepam, metizolam and nitrazolam". Journal of Mass Spectrometry. 51 (11): 1080–1089. Bibcode:2016JMSp...51.1080M. doi:10.1002/jms.3840. PMID 27535017.
  • ^ Kintz P, Richeval C, Jamey C, Ameline A, Allorge D, Gaulier JM, Raul JS (July 2017). "Detection of the designer benzodiazepine metizolam in urine and preliminary data on its metabolism". Drug Testing and Analysis. 9 (7): 1026–1033. doi:10.1002/dta.2099. PMID 27671107.
  • ^ "Desmethyletizolam". New Synthetic Drugs Database. Archived from the original on 2016-06-25. Retrieved 2016-01-16.
  • ^ "31 nya ämnen kan klassas som narkotika eller hälsofarlig vara" (in Swedish). Folkhälsomyndigheten. November 2015.
    • Stub icon

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    • Retrieved from "https://en.wikipedia.org/w/index.php?title=Metizolam&oldid=1178608659"
    Categories: 
    ●Chloroarenes
     ●Designer drugs
     ●GABAA receptor positive allosteric modulators
     ●Hypnotics
     ●Thienotriazolodiazepines
     ●Sedative stubs
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    ●This page was last edited on 4 October 2023, at 19:11 (UTC).
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