An NSAID used in animals
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Carprofen

Item No. 16409

Technical Information
Formal Name
6-chloro-α-methyl-9H-carbazole-2-acetic acid
CAS Number
53716-49-7
Synonyms
  • Carprodyl
  • NSC 297935
Molecular Formula
C15H12ClNO2
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 20 mg/mlDMSO: 30 mg/mlDMSO:PBS(pH7.2) (1:1): 0.5 mg/mlEthanol: 20 mg/ml
λmax
239, 263, 301, 332, 345 nm
SMILES
CC(C(O)=O)C1=CC(NC2=C3C=C(Cl)C=C2)=C3C=C1
InChi Code
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)
InChi Key
PUXBGTOOZJQSKH-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Carprofen is a non-steroidal anti-inflammatory drug (NSAID) commonly used in animals to combat pain and inflammation, particularly as associated with osteoarthritis.1,2 Like many NSAIDs, carprofen inhibits both cyclooxygenases COX-1 and COX-2 (IC50s = 22.3 and 3.9 µM, respectively).3,4 It also inhibits fatty acid amide hydrolase (IC50 = 74 µM), blocking the metabolism of the cannabinoid receptor ligand, arachidonoyl ethanolamide (Item No. 90050).4,5

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Malek, S., Sample, S.J., Schwartz, Z., et alEffect of analgesic therapy on clinical outcome measures in a randomized controlled trial using client-owned dogs with hip osteoarthritis. BMC Vet. Res. 8, 185 (2012).

    2. Brown, D.C., Boston, R.C., Coyne, J.C., et alAbility of the canine brief pain inventory to detect response to treatment in dogs with osteoarthritis. J. Am. Vet. Med. Assoc. 233(8), 1278-1283 (2008).

    3. Li, J., Lynch, M.P., DeMello, K.L., et alIn vitro and in vivo profile of 2-(3-di-fluoromethyl-5-phenylpyrazol-1-yl)-5-methanesulfonylpyride, a potent, selective, and orally active canine COX-2 inhibitor. Bioorg. Med. Chem. 13(5), 1805-1809 (2005).

    4. Favia, A.D., Habrant, D., Scarpelli, R., et alIdentification and characterization of carprofen as a multi-target FAAH/COX inhibitor. J. Med. Chem. 55(20), 8807-8826 (2012).

    5. Bertolacci, L., Romeo, E., Veronesi, M., et alA binding site for nonsteroidal anti-inflammatory drugs in fatty acid amide hydrolase. J. Am. Chem. Soc. 135(1), 22-25 (2013).