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teknopedia

Flag Counter
  2. World Encyclopedia
  3. Demoxepam - Wikipedia
Demoxepam - Wikipedia
From Wikipedia, the free encyclopedia

Demoxepam
Pharmacokinetic data
Elimination half-life35–40 hours
Identifiers
  • 7-Chloro-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepin-2-one-4-oxide
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.012.287 Edit this at Wikidata
Chemical and physical data
FormulaC15H11ClN2O2
Molar mass286.71 g·mol−1
3D model (JSmol)
  • ClC1=CC2=C(NC(C[N+]([O-])=C2C3=CC=CC=C3)=O)C=C1
  • InChI=1S/C15H11ClN2O2/c16-11-6-7-13-12(8-11)15(10-4-2-1-3-5-10)18(20)9-14(19)17-13/h1-8H,9H2,(H,17,19) checkY
  • Key:GGRWZBVSUZZMKS-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Demoxepam[1] is a drug which is a benzodiazepine derivative. It is a metabolite of chlordiazepoxide[2] and has anticonvulsant properties[3][4] and presumably other characteristic benzodiazepine properties.

See also

References

  1. ^ US Patent 3136815
  2. ^ Greenblatt DJ, Shader RI, MacLeod SM, Sellers EM (1978). "Clinical pharmacokinetics of chlordiazepoxide". Clinical Pharmacokinetics. 3 (5): 381–94. doi:10.2165/00003088-197803050-00004. PMID 359214.
  3. ^ "nortetrazepam". psychotropics.dk. 2003. Retrieved 7 December 2009.
  4. ^ "LIST OF INTERNATIONAL NON-PROPRIETARY NAMES (INNS), PROVIDED FOR PHARMACEUTICAL SUBSTANCES BY THE WORLD HEALTH ORGANIZATION, WHICH ARE FREE OF DUTY" (PDF). Official Journal of the European Communities. eur-lex.europa.eu. 23 October 2001. Retrieved 7 December 2009.
Stub icon

This sedative-related article is a stub. You can help Wikipedia by adding missing information.

Sunting pranala
url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url 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