Musiol Robert
Institute of Chemistry, University of Silesia in Katowice, 75 Pulku Piechoty 1A, 41-500, Chorzow, Poland.
Med Chem. 2020;16(2):141-154. doi: 10.2174/1573406415666190603103012.
Styrylquinolines are characteristic fully aromatic compounds with flat, rather lipophilic structures. The first reports on their synthesis and biological activity were published roughly a century ago. However, their low selectivity, unfavorable toxicity and problems with their mechanism of action significantly hampered their development. As a result, they have been abandoned for most of the time since they were discovered.
Their renaissance was observed by the antiretroviral activity of several styrylquinoline derivatives that have been reported to be HIV integrase inhibitors. Subsequently, other activities such as their antifungal and anticancer abilities have also been revisited.
In the present review, the spectrum of the activity of styrylquinolines and their use in drug design is presented and analyzed.
New properties and applications that were reported recently have re-established styrylquinolines within medicinal and material chemistry. The considerable increase in the number of published papers regarding their activity spectrum will ensure further discoveries in the field.
Styrylquinolines have earned a much stronger position in medicinal chemistry due to the discovery of their new activities, profound mechanisms of action and as drug candidates in clinical trials.
苯乙烯基喹啉是具有扁平、相当亲脂性结构的典型全芳香族化合物。关于它们的合成和生物活性的首次报道大约在一个世纪前发表。然而,它们的低选择性、不良毒性以及作用机制方面的问题严重阻碍了它们的发展。因此,自发现以来的大部分时间里它们都被弃用了。
几种苯乙烯基喹啉衍生物具有抗逆转录病毒活性,据报道它们是HIV整合酶抑制剂,由此人们观察到了它们的复兴。随后,它们的其他活性,如抗真菌和抗癌能力也被重新审视。
在本综述中,介绍并分析了苯乙烯基喹啉的活性谱及其在药物设计中的应用。
最近报道的新性质和新应用在药物化学和材料化学领域重新确立了苯乙烯基喹啉的地位。关于它们活性谱的已发表论文数量大幅增加,这将确保该领域有更多的发现。
由于发现了苯乙烯基喹啉的新活性、深刻的作用机制以及作为临床试验中的候选药物,它们在药物化学领域赢得了更稳固的地位。