Carprofen

Carprofen
Two-dimensional monochrome diagram showing the structure of the molecule of Carprofen, uing the hexagonal style to depict a chemical compound.
Carprofen molecule
Clinical data
AHFS/Drugs.comFDA Professional Drug Information
Routes of
administration
Oral, injection
ATCvet code
Legal status
Legal status
  • US: Veterinary use only[1]
Pharmacokinetic data
Protein bindingHigh (99%)
Elimination half-lifeApproximately 8 h (range 4.5–9.8 h) in dogs
Identifiers
  • (RS)-2-(6-Chloro-9H-carbazol-2-yl)propanoic acid
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.053.357 Edit this at Wikidata
Chemical and physical data
FormulaC15H12ClNO2
Molar mass273.72 g·mol−1
3D model (JSmol)
ChiralityRacemic mixture
  • CC(C1=CC=C2C(NC3=CC=C(C=C32)Cl)=C1)C(O)=O
  • InChI=1S/C15H12ClNO2/c1-8(15(18)19)9-2-4-11-12-7-10(16)3-5-13(12)17-14(11)6-9/h2-8,17H,1H3,(H,18,19) checkY
  • Key:PUXBGTOOZJQSKH-UHFFFAOYSA-N checkY
  (verify)
A 100 mg Rimadyl tablet approximately 19 mm (0.75 in) wide by 8.6 mm (0.34 in) thick, as sold in the USA.

Carprofen is a nonsteroidal anti-inflammatory drug (NSAID) of the carbazole and propionic acid class that was previously for use in humans and animals but is now only available to veterinarians for prescribing as a supportive treatment for various conditions in animals.[1] Carprofen reduces inflammation by inhibition of COX-1 and COX-2; its specificity for COX-2 varies from species to species.[1] Marketed under many brand names worldwide,[2] carprofen is used as a treatment for inflammation and pain, including joint pain and postoperative pain.[1]

  1. ^ a b c d "Rimadyl (carprofen) prescribing information leaflet" (PDF). www2.ZoetisUS.com. Zoetis Inc. Retrieved 5 February 2022.
  2. ^ "International brand names for Carprofen". www.Drugs.com. Drugs.com. Retrieved 4 October 2017.