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Fospropofol information


Fospropofol
Clinical data
AHFS/Drugs.comMonograph
License data
  • US FDA: Fospropofol
Pregnancy
category
  • B
Dependence
liability
unknown
Routes of
administration
Intravenous
ATC code
  • N01
Legal status
Legal status
  • US: Schedule IV
Pharmacokinetic data
Protein binding98%[1]
MetabolismHepatic glucuronidation
Elimination half-life0.81 hours[1]
ExcretionRenal
Identifiers
IUPAC name
  • disodium [2,6-di(propan-2-yl)phenoxy]methyl phosphate[2]
CAS Number
  • 258516-89-1 checkY
    258516-87-9 (disodium salt)
PubChem CID
  • 3038498
DrugBank
  • DB06716 ☒N
ChemSpider
  • 2302062 ☒N
UNII
  • LZ257RZP7K
KEGG
  • D04257 checkY
ChEMBL
  • ChEMBL1201766 ☒N
CompTox Dashboard (EPA)
  • DTXSID50870295 Edit this at Wikidata
Chemical and physical data
FormulaC13H21O5P
Molar mass288.280 g·mol−1
3D model (JSmol)
  • Interactive image
SMILES
  • CC(C)c1cccc(c1OCOP(=O)(O)O)C(C)C
InChI
  • InChI=1S/C13H21O5P/c1-9(2)11-6-5-7-12(10(3)4)13(11)17-8-18-19(14,15)16/h5-7,9-10H,8H2,1-4H3,(H2,14,15,16) ☒N
  • Key:QVNNONOFASOXQV-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Fospropofol (INN[3]), often used as the disodium salt (trade name Lusedra[4]) is an intravenous sedative-hypnotic agent. It is currently approved for use in sedation of adult patients undergoing diagnostic or therapeutic procedures such as endoscopy.

  1. ^ a b "LUSEDRA (fospropofol disodium) Injection" (PDF). Woodcliff Lake, New Jersey: Eisai Inc. October 2009. Archived from the original (PDF) on 22 November 2010. Retrieved 2 August 2010.
  2. ^ "Fospropofol disodium". PubChem Compound. Bethesda, Maryland: U.S. National Library of Medicine. Retrieved 9 February 2017.
  3. ^ "Recommended INNs 2006, pt 56" (PDF). World Health Organization. Retrieved 20 April 2016.
  4. ^ "FDA Approves Fospropofol and Follows ASAs Labeling Recommendation". American Society of Anesthesiologists. 2008-12-15. Archived from the original on 2011-05-26. Retrieved 2011-03-30.

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