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作为15-脂氧合酶抑制剂的苯甲酰肼及其重氮烯衍生物的简便快速制备方法。

Easy and rapid preparation of benzoylhydrazides and their diazene derivatives as inhibitors of 15-lipoxygenase.

作者信息

Tirapegui Cristian, Acevedo-Fuentes Williams, Dahech Pablo, Torrent Claudia, Barrias Pablo, Rojas-Poblete Macarena, Mascayano Carolina

机构信息

Departamento de Química, Facultad de Ciencias, Universidad de Chile, Casilla 653, Santiago, Chile; Facultad de Química y Biología, Universidad de Santiago de Chile, Casilla 40, correo 33, Santiago, Chile.

Departamento de Química, Facultad de Ciencias, Universidad de Chile, Casilla 653, Santiago, Chile.

出版信息

Bioorg Med Chem Lett. 2017 Apr 15;27(8):1649-1653. doi: 10.1016/j.bmcl.2017.03.017. Epub 2017 Mar 8.

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 IC 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.

摘要

通过苯甲酸与4-取代苯肼的无溶剂缩合反应制备了两个系列的二氮杂衍生物,以获得苯肼酰(HYD系列),并通过氧化这些化合物得到相应的苯甲酰二氮烯(DIA系列)。在FRAP和CUPRAC分析中,对这两组化合物进行了大豆15-脂氧合酶活性抑制剂和抗氧化能力的评估。两个系列中最有效的抑制剂的IC值在低微摩尔范围内。动力学研究表明,至少活性较高的化合物是竞争性抑制剂。对接结果表明,最有效的抑制剂与活性位点中的Ile-839和铁强烈相互作用。

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