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The 2′-Trifluoromethyl Analogue of Indomethacin Is a Potent and Selective COX-2 Inhibitor
[Image: see text] Indomethacin is a potent, time-dependent, nonselective inhibitor of the cyclooxygenase enzymes (COX-1 and COX-2). Deletion of the 2′-methyl group of indomethacin produces a weak, reversible COX inhibitor, leading us to explore functionality at that position. Here, we report that su...
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| Huvudupphovsmän: | , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
American Chemical Society
2013
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| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3654564/ https://ncbi.nlm.nih.gov/pubmed/23687559 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ml400066a |
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