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Carprofen

Catalog No. DB00821 Name DrugBank
CAS Number 53716-49-7 Website http://www.ualberta.ca/
M. F. C15H12ClNO2 Telephone (780) 492-3111
M. W. 273.71428 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 700

SYNONYMS

IUPAC name
2-(6-chloro-9H-carbazol-2-yl)propanoic acid
IUPAC Traditional name
carprofen
Brand Name
Ridamyl
Rimadyl
Synonyms
Carprofenum [inn-latin]
6-Chloro-alpha-methylcarbazole-2-acetic acid
Carprofene [inn-french]
Carprofeno [inn-spanish]
6-Chloro-alpha-methyl-9H-carbazole-2-acetic acid
2-(6-Chloro-9H-carbazol-2-yl)propanoic acid

DATABASE IDS

CAS Number 53716-49-7
PubChem SID 46505357
PubChem CID 2581

PROPERTIES

Hydrophobicity(logP) 3.8
Solubility Practically insoluble at 25oC

DETAILS

Description (English)
Item Information
Drug Groups approved
Description Carprofen is a non-steroidal anti-inflammatory drug (NSAID) that is used by veterinarians as a supportive treatment for the relief of arthritic symptoms in geriatric dogs. Carprofen was previously used in human medicine for over 10 years (1985-1995). It was generally well tolerated, with the majority of adverse effects being mild, such as gastro-intestinal pain and nausea, similar to those recorded with aspirin and other non-steroidal anti-inflammatory drugs. It is no longer marketed for human usage, after being withdrawn on commercial grounds. [Wikipedia]
Indication For use as a pain reliever in the treatment of joint pain and post-surgical pain.
Pharmacology Carprofen is a non-steroidal anti-inflammatory drug (NSAID) of the propionic acid class that includes ibuprofen, naproxen, and ketoprofen. It is no longer used in the clinical setting, but is approved for use in dogs. Carprofen is non-narcotic and has characteristic analgesic and antipyretic activity approximately equipotent to indomethacin in animal models.
Toxicity Symptoms of NSAID overdose include dizziness and nystagmus. Oral LD50 in mouse and rat is 282 mg/kg and 149 mg/kg, respectively.
Affected Organisms
Humans and other mammals
Biotransformation Hepatic.
Absorption Rapidly and nearly completely absorbed (more than 90% bioavailable) when administered orally.
Half Life Approximately 8 hours (range 4.5–9.8 hours) in dogs.
Protein Binding High (99%)
External Links
Wikipedia

REFERENCES