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Chemical and biological investigation of N-hydroxy-valdecoxib: An active metabolite of valdecoxib
- Source :
- Bioorganic & Medicinal Chemistry. 16:5322-5330
- Publication Year :
- 2008
- Publisher :
- Elsevier BV, 2008.
-
Abstract
- The inhibition of cyclooxygenase enzymes plays an important role in the treatment of inflammatory diseases. N-Hydroxy-4-(5-methyl-3-phenylisoxazol-4-yl)benzenesulfonamide (3)-a primary metabolite of the highly selective COX-2 inhibitor valdecoxib-was synthesized and stabilized as its monohydrate (3a.H(2)O). The anti-inflammatory properties of 3a.H(2)O were investigated in carrageenan-induced edema and in acute and chronic pain models. Based on our biological investigation, we conclude that N-hydroxy-valdecoxib 3a is an active metabolite of valdecoxib.
- Subjects :
- Male
Models, Molecular
Time Factors
Metabolite
Clinical Biochemistry
Pharmaceutical Science
Pharmacology
Carrageenan
Crystallography, X-Ray
Biochemistry
chemistry.chemical_compound
Drug Discovery
Edema
Pain Measurement
Sulfonamides
Molecular Structure
biology
Chemistry
Anti-Inflammatory Agents, Non-Steroidal
Stereoisomerism
Biological activity
Recombinant Proteins
Hyperalgesia
Enzyme inhibitor
Molecular Medicine
Rabbits
medicine.drug
Stereochemistry
Analgesic
Pain
medicine
Animals
Humans
Rats, Wistar
Molecular Biology
Active metabolite
Inflammation
Cyclooxygenase 2 Inhibitors
Dose-Response Relationship, Drug
Organic Chemistry
Primary metabolite
Isoxazoles
Valdecoxib
Rats
Disease Models, Animal
Cyclooxygenase 2
Cyclooxygenase 1
biology.protein
Cattle
Cyclooxygenase
Subjects
Details
- ISSN :
- 09680896
- Volume :
- 16
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry
- Accession number :
- edsair.doi.dedup.....cdd35aab7e4ac679c0c76f8b119290db
- Full Text :
- https://doi.org/10.1016/j.bmc.2008.02.088