摘要
杂环化合物由于其结构和化学多样性,代表了抗癌研究和药物发现的重要目标。 在核心结构中存在氧和氮原子的恶唑能够与不同的酶和受体进行各种类型的相互作用,从而有利于发现新药。 这篇综述的目的是描述基于恶唑基化合物在抗癌研究中的最新报道,并参考新发现的基于异/恶唑基的药物,其合成以及最具生物活性的衍生物的评估。 还报道了相应的脱氢衍生物,即异/恶唑啉和异/恶唑烷。
关键词: 恶唑,异恶唑,恶唑啉,恶唑烷,抗癌活性,合成。
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