| Literature DB >> 25771032 |
Nikolaos Eleftheriadis1, Stephanie Thee1, Johan te Biesebeek1, Petra van der Wouden1, Bert-Jan Baas2, Frank J Dekker3.
Abstract
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 Ki 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.Entities:
Keywords: Enzyme kinetics; Expression; Inhibitor; Lipoxygenase; Salicylate
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Year: 2015 PMID: 25771032 DOI: 10.1016/j.ejmech.2015.03.007
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514