Features of the synthesis and biological evaluation of 3-(carboxyphenyl)chromones

O. Shablykina, V. Moskvina, V. Khilya
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引用次数: 1

Abstract

Flavonoids and their derivatives have historically been a source of therapeutic agents. Every year, more and more data is published on new flavonoid compounds, both synthetic and isolated from natural sources, and their innumerable physiological and pharmacological activities. This review presents synthetic routes towards 3-(carboxyphenyl)chromones and evaluation of their biological activity as published in both journal and patent literature. We have focused specifically on the 3-(carboxyphenyl)chromones, because while methods of synthesis and biological activity of 2(3)-substituted and 2,3-disubstituted chromones are well studied, literature data on isoflavones containing a carboxyl, ester, or amide group in ring B is scarce and fragmentary. The presented generalization of synthetic strategies and biological activity of 3-(carboxyphenyl)chromone derivatives demonstrates that this class of compounds can be targeted for discovery of new drugs and can be readily prepared owing to recent advances in synthetic organic and medicinal chemistry.
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3-(羧基苯基)色酮的合成特点及生物学评价
黄酮类化合物及其衍生物历来是治疗剂的来源。每年都有越来越多的数据发表在新的类黄酮化合物,无论是合成的还是从天然来源分离的,以及它们无数的生理和药理活性。本文综述了3-(羧基苯基)色素的合成路线及其生物活性的评价,并对已发表的期刊和专利文献进行了综述。我们特别关注3-(羧基苯基)色素,因为虽然2(3)取代和2,3-二取代色素的合成方法和生物活性已经得到了很好的研究,但关于在B环中含有羧基、酯或酰胺基团的异黄酮的文献资料很少,而且是片段的。3-(羧基苯基)色素衍生物的合成策略和生物活性的概括表明,由于合成有机化学和药物化学的最新进展,这类化合物可以很容易地制备,并且可以成为发现新药的目标。
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