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Suprofen

From Wikipedia, the free encyclopedia
Non-steroidal anti-inflammatory drug

Pharmaceutical compound
Suprofen
Clinical data
AHFS/Drugs.comMicromedex Detailed Consumer Information
Routes of
administration
Oral, eye drops
ATC code
Legal status
Legal status
  • Discontinued
Pharmacokinetic data
Protein binding20%
Identifiers
  • (RS)-2-[4-(2-thienylcarbonyl)phenyl]propanoic acid
CAS Number
PubChemCID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.050.071Edit this at Wikidata
Chemical and physical data
FormulaC14H12O3S
Molar mass260.31 g·mol−1
3D model (JSmol)
  • O=C(c1ccc(cc1)C(C(=O)O)C)c2sccc2
  • InChI=1S/C14H12O3S/c1-9(14(16)17)10-4-6-11(7-5-10)13(15)12-3-2-8-18-12/h2-9H,1H3,(H,16,17) ☒N
  • Key:MDKGKXOCJGEUJW-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Suprofen is anonsteroidal anti-inflammatory drug (NSAID) developed byJanssen Pharmaceutica[1] that was marketed as 1% eye drops under thetrade nameProfenal.

Uses

[edit]

Suprofen was originally used astablet, but oral uses have been discontinued due torenal effects.[2] It was subsequently used exclusively as atopicalophthalmic solution, typically to preventmiosis during and after ophthalmicsurgery.[3] This application has been discontinued as well, at least in the US.[4]

References

[edit]
  1. ^DE 2353357, Janssen PA, Van Daele GH, Boey JM, "Antiphlogistic aroyl-substituted phenylacetic acid derivatives", issued 1974 
  2. ^Nies AS (1988). "Renal Effects of Nonsteroidal Anti-Inflammatory Drugs".Basis for Variability of Response to Anti-Rheumatic Drugs. Vol. 24. pp. 95–106.doi:10.1007/978-3-0348-9160-8_9 (inactive 12 July 2025).ISBN 978-3-0348-9931-4.PMID 3142236.{{cite book}}:|journal= ignored (help)CS1 maint: DOI inactive as of July 2025 (link)
  3. ^"Pharmacy Compounding".Guidance for FDA Staff and Industry Compliance Policy Guides Manual. U.S. Food and Drug Administration. Archived fromthe original on 1 January 2009.
  4. ^"Suprofen ophthalmic".Drugs.com. Archived fromthe original on 2021-09-09. Retrieved2018-01-23.
pyrazolones /
pyrazolidines
salicylates
acetic acid derivatives
and related substances
oxicams
propionic acid
derivatives (profens)
n-arylanthranilic
acids (fenamates)
COX-2 inhibitors
(coxibs)
other
NSAID
combinations
Key:underline indicates initially developed first-in-class compound of specific group;#WHO-Essential Medicines;withdrawn drugs;veterinary use.
Receptor
(ligands)
DP (D2)Tooltip Prostaglandin D2 receptor
DP1Tooltip Prostaglandin D2 receptor 1
DP2Tooltip Prostaglandin D2 receptor 2
EP (E2)Tooltip Prostaglandin E2 receptor
EP1Tooltip Prostaglandin EP1 receptor
EP2Tooltip Prostaglandin EP2 receptor
EP3Tooltip Prostaglandin EP3 receptor
EP4Tooltip Prostaglandin EP4 receptor
Unsorted
FP (F)Tooltip Prostaglandin F receptor
IP (I2)Tooltip Prostacyclin receptor
TP (TXA2)Tooltip Thromboxane receptor
Unsorted
Enzyme
(inhibitors)
COX
(
PTGS)
PGD2STooltip Prostaglandin D synthase
PGESTooltip Prostaglandin E synthase
PGFSTooltip Prostaglandin F synthase
PGI2STooltip Prostacyclin synthase
TXASTooltip Thromboxane A synthase
Others
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