首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >2-(4-(Biphenyl-4-ylamino)-6-chloropyrimidin-2-ylthio)octanoic acid (HZ52) – a novel type of 5-lipoxygenase inhibitor with favourable molecular pharmacology and efficacy in vivo
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2-(4-(Biphenyl-4-ylamino)-6-chloropyrimidin-2-ylthio)octanoic acid (HZ52) – a novel type of 5-lipoxygenase inhibitor with favourable molecular pharmacology and efficacy in vivo

机译:2-(4-(联苯-4-基氨基)-6-氯嘧啶-2-基硫基)辛酸(HZ52)–一种新型的5-脂氧合酶抑制剂在体内具有良好的分子药理作用和功效

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摘要

BACKGROUND AND PURPOSE5-Lipoxygenase (5-LO) is the key enzyme in the biosynthesis of pro-inflammatory leukotrienes (LTs) representing a potential target for pharmacological intervention with inflammation and allergic disorders. Although many LT synthesis inhibitors are effective in simple in vitro test systems, they frequently fail in vivo due to lack of efficacy. Here, we attempted to assess the pharmacological potential of the previously identified 5-LO inhibitor 2-(4-(biphenyl-4-ylamino)-6-chloropyrimidin-2-ylthio)octanoic acid (HZ52).
机译:背景和目的5-脂氧合酶(5-LO)是促炎性白三烯(LTs)生物合成中的关键酶,代表了针对炎症和过敏性疾病进行药理干预的潜在目标。尽管许多LT合成抑制剂在简单的体外测试系统中均有效,但由于缺乏功效,它们在体内经常失败。在这里,我们试图评估以前确定的5-LO抑制剂2-(4-(联苯-4-基氨基)-6-氯嘧啶-2-基硫基)辛酸(HZ52)的药理潜力。

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