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Biochemically based design of cyclooxygenase-2 (COX-2) inhibitors: Facile conversion of nonsteroidal antiinflammatory drugs to potent and highly selective COX-2 inhibitors

All nonsteroidal antiinflammatory drugs (NSAIDs) inhibit the cyclooxygenase (COX) isozymes to different extents, which accounts for their anti-inflammatory and analgesic activities and their gastrointestinal side effects. We have exploited biochemical differences between the two COX enzymes to ident...

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Bibliografske podrobnosti
Main Authors: Kalgutkar, Amit S., Crews, Brenda C., Rowlinson, Scott W., Marnett, Alan B., Kozak, Kevin R., Remmel, Rory P., Marnett, Lawrence J.
Format: Artigo
Jezik:Inglês
Izdano: The National Academy of Sciences 2000
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC15432/
https://ncbi.nlm.nih.gov/pubmed/10639181
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