Correction: Structural basis for selective inhibition of cyclooxygenase-2 by anti-inflammatory agents

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Structural and functional basis of cyclooxygenase inhibition.

Brief History. The use of medicinal substances for the treatment of pain and fever dates to ancient Egyptian and Grecian civilizations, where dried myrtle leaves or bitter extracts from the bark of poplar trees were used to treat back and abdominal pain. The Ebers papyrus from ancient Egypt (1850 B.C.) is the oldest preserved medical text and contains the first record documenting the use of pla...

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Anti-inflammatory, anti-proliferative and antioxidant profiles of selective cyclooxygenase-2 inhibition as chemoprevention for rat bladder carcinogenesis.

PURPOSE To evaluate the efficacy of a selective cyclooxygenase-2 (COX-2) inhibitor in rat bladder cancer chemoprevention, as well as to assess the relevance of inflammation, proliferation and oxidative stress in tumor growth and in its prevention. RESULTS The main findings were: (I) the incidence of carcinoma was: control: 0% (0/8); BBN: 65% (13/20); CEL: 0% (0/8) and BBN + CEL: 12.5% (1/8); ...

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The structural basis of endocannabinoid oxygenation by cyclooxygenase-2.

The cyclooxygenases (COX-1 and COX-2) oxygenate arachidonic acid (AA) in the committed step of prostaglandin biogenesis. Substitutions of I434V, H513R, and I523V constitute the only differences in residues lining the cyclooxygenase channel between COX-1 and COX-2. These changes create a hydrophobic pocket in COX-2, with Arg-513 located at the base of the pocket, which has been exploited in the ...

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Molecular basis of cyclooxygenase enzymes (COXs) selective inhibition.

The widely used nonsteroidal anti-inflammatory drugs block the cyclooxygenase enzymes (COXs) and are clinically used for the treatment of inflammation, pain, and cancers. A selective inhibition of the different isoforms, particularly COX-2, is desirable, and consequently a deeper understanding of the molecular basis of selective inhibition is of great demand. Using an advanced computational tec...

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Up-regulation of cyclooxygenase-2 by inhibition of cyclooxygenase-1: a key to nonsteroidal anti-inflammatory drug-induced intestinal damage.

Nonsteroidal anti-inflammatory drugs (NSAIDs) induce gastrointestinal ulceration as the adverse reaction. This effect of NSAIDs is attributable to endogenous prostaglandin (PG) deficiency caused by inhibition of cyclooxygenase (COX), yet the relation between COX inhibition and the gastrointestinal ulcerogenic property of NSAIDs remains controversial. Using selective COX inhibitors, we examined ...

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ژورنال

عنوان ژورنال: Nature

سال: 1997

ISSN: 0028-0836,1476-4687

DOI: 10.1038/385555b0