Identification of 6-benzyloxysalicylates as a novel class of inhibitors of 15-lipoxygenase-1
European Journal of Medicinal Chemistry, ISSN: 0223-5234, Vol: 94, Page: 265-275
2015
- 26Citations
- 44Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations26
- Citation Indexes26
- 26
- CrossRef20
- Captures44
- Readers44
- 44
Article Description
Lipoxygenases metabolize polyunsaturated fatty acids into signalling molecules such as leukotrienes and lipoxins. 15-lipoxygenase-1 (15-LOX-1) is an important mammalian lipoxygenase and plays a crucial regulatory role in several respiratory diseases such as asthma, COPD and chronic bronchitis. Novel potent and selective inhibitors of 15-LOX-1 are required to explore the role of this enzyme in drug discovery. In this study we describe structure activity relationships for 6-benzyloxysalicylates as inhibitors of human 15-LOX-1. Kinetic analysis suggests competitive inhibition and the binding model of these compounds can be rationalized using molecular modelling studies. The most potent derivative 37a shows a K i value of 1.7 μM. These structure activity relationships provide a basis to design improved inhibitors and to explore 15-LOX-1 as a drug target.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S022352341500166X; http://dx.doi.org/10.1016/j.ejmech.2015.03.007; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84952900111&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/25771032; https://linkinghub.elsevier.com/retrieve/pii/S022352341500166X; https://dx.doi.org/10.1016/j.ejmech.2015.03.007
Elsevier BV
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