首页> 外文期刊>Journal of Medicinal Chemistry >2?Aminonicotinic Acid 1?Oxides Are Chemically Stable Inhibitors of Quinolinic Acid Synthesis in the Mammalian Brain: A Step toward New Antiexcitotoxic Agents
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2?Aminonicotinic Acid 1?Oxides Are Chemically Stable Inhibitors of Quinolinic Acid Synthesis in the Mammalian Brain: A Step toward New Antiexcitotoxic Agents

机译:2?氨基烟酸1?氧化物是哺乳动物大脑中喹啉酸合成的化学稳定抑制剂:迈向新型抗兴奋剂的一步

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摘要

3-Hydroxyanthranilic acid 3,4-dioxygenase (3-HAO) is the enzyme responsible for the production of the neurotoxic tryptophan metabolite quinolinic acid (QUIN). Elevated brain levels of QUIN are observed in several neurodegenerative diseases, but pharmacological investigation on its role in the pathogenesis of these conditions is difficult because only one class of substrate-analogue 3-HAO inhibitors, with poor chemical stability, has been reported so far. Here we describe the design, synthesis, and biological evaluation of a novel class of chemically stable inhibitors based on the 2-aminonicotinic acid 1-oxide nucleus. After the preliminary in vitro evaluation of newly synthesized compounds using brain tissue homogenate, we selected the most active inhibitor and showed its ability to acutely reduce the production of QUIN in the rat brain in vivo. These findings provide a novel pharmacological tool for the study of the mechanisms underlying the onset and propagation of neurodegenerative diseases.
机译:3-羟基邻氨基苯甲酸3,4-二加氧酶(3-HAO)是负责产生神经毒性色氨酸代谢物喹啉酸(QUIN)的酶。在几种神经退行性疾病中观察到QUIN的脑水平升高,但是很难对其药理学研究其在这些疾病的发病机理中的作用,因为迄今为止仅报道了一类化学稳定性较差的底物类似物3-HAO抑制剂。在这里,我们描述了基于2-氨基烟酸1-氧化物核的一类新型化学稳定抑制剂的设计,合成和生物学评估。在使用脑组织匀浆对新合成的化合物进行了初步的体外评估后,我们选择了活性最强的抑制剂,并显示了其在大鼠体内急性减少QUIN产生的能力。这些发现为研究神经退行性疾病的发病和传播的潜在机制提供了一种新颖的药理学工具。

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