Synthesis and SAR studies of 3-allyl-4-prenyloxyaniline amides as potent 15-lipoxygenase inhibitors

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• 作者：Atena Jabbari ; Mahdieh Davoodnejad ; Maliheh Alimardani ; Amir Assadiesk ; ar ; Ali Sadeghian ; Hadi Safdari ; Jebraeel Movaffagh ; Hamid Sadeghian
• 关键词：SLO ; MBTH ; DMAB ; Radical scavenger ; DPPH
• 刊名：Bioorganic and Medicinal Chemistry
• 出版年：2012
• 出版时间：15 September, 2012
• 年：2012
• 卷：20
• 期：18
• 页码：5518-5526
• 全文大小：763 K

文摘

15-Lipoxygenases are one of the nonheme iron-containing proteins with ability of unsaturated lipid peroxidation in animals and plants. The critical role of the enzymes in formation of inflammations, sensitivities and some of cancers has been demonstrated in mammalians. Importance of the 15-lipoxygenases leads to development of mechanistic studies, products analysis and synthesis of their inhibitors. In this work new series of the 3-allyl-4-allyoxyaniline amides and 3-allyl-4-prenyloxyaniline amides were designed, synthesized and their inhibitory potency against soybean 15-lipoxygenase were determined. Among the synthetic amides, 3-allyl-4-(farnesyloxy)-adamantanilide showed the most potent inhibitory activity by IC₅₀ value of 0.69 ¦ÌM. SAR studies showed that in spite of prenyl length increases, the effects of the amide size and its electronic properties on the inhibitory potency became predominant. The SAR studies was also showed that the orientation of allyl and prenyloxy moieties toward Fe core of the SLO active site pocket is the most suitable location for enzyme inhibition.