| Literature DB >> 28318946 |
Cristian Tirapegui1, Williams Acevedo-Fuentes2, Pablo Dahech3, Claudia Torrent3, Pablo Barrias3, Macarena Rojas-Poblete4, Carolina Mascayano3.
Abstract
Two series of diaza derivatives were prepared by solvent-free condensation of benzoic acid and 4-substituted phenylhydrazines in order to obtain phenylhydrazides (HYD series) and, by oxidation of these compounds, the corresponding benzoyldiazenes (DIA series). Both sets were evaluated as inhibitors of soybean 15-lipoxygenase activity and antioxidant capability in the FRAP and CUPRAC assays. The most potent inhibitors of both series exhibited IC50 values in the low micromolar range. Kinetic studies showed that at least the more active compounds were competitive inhibitors. Docking results indicated that the most potent inhibitor interacts strongly with Ile-839 and iron in the active site.Entities:
Keywords: 15-Lipoxygenase inhibition; Antioxidant capability; Benzoyldiazene; Lipophilicity; Phenylhydrazides
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Year: 2017 PMID: 28318946 DOI: 10.1016/j.bmcl.2017.03.017
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823