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This is an old revision of this page, as edited by Beetstra (talk | contribs) at 11:46, 16 February 2012 (Saving copy of the {{drugbox}} taken from revid 477128398 of page Ketamine for the Chem/Drugbox validation project (updated: '').). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Revision as of 11:46, 16 February 2012 by Beetstra (talk | contribs) (Saving copy of the {{drugbox}} taken from revid 477128398 of page Ketamine for the Chem/Drugbox validation project (updated: '').)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)
This page contains a copy of the infobox ({{drugbox}}) taken from revid 477128398 of page Ketamine with values updated to verified values.
Ketamine
Clinical data
AHFS/Drugs.comConsumer Drug Information
Pregnancy
category
  • B
Dependence
liability		Medium
Routes of
administration		IV, IM, Insufflated, oral, topical
ATC code
Legal status
Legal status
Pharmacokinetic data
MetabolismHepatic, primarily by CYP3A4
Elimination half-life2.5–3 hours.
Excretionrenal (>90%)
Identifiers
IUPAC name
  • (RS)-2-(2-Chlorophenyl)-2-(methylamino)cyclohexanone
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
Chemical and physical data
FormulaC13H16ClNO
Molar mass237.725 g/mol g·mol
3D model (JSmol)
Melting point262 °C (504 °F)
SMILES
  • CNC1(CCCCC1=O)c2ccccc2Cl
InChI
  • InChI=1S/C13H16ClNO/c1-15-13(9-5-4-8-12(13)16)10-6-2-3-7-11(10)14/h2-3,6-7,15H,4-5,8-9H2,1H3
  • Key:YQEZLKZALYSWHR-UHFFFAOYSA-N
  (verify)
  1. Hijazi Y, Boulieu R (2002). "Contribution of CYP3A4, CYP2B6, and CYP2C9 isoforms to N-demethylation of ketamine in human liver microsomes". Drug Metabolism and Disposition. 30 (7): 853–8. doi:10.1124/dmd.30.7.853. PMID 12065445. {{cite journal}}: Unknown parameter |month= ignored (help)