Synthesis A New Bis Oxazine and Thiazine Derivatives and Study Their Biological Activities

Dina Saleem M. Ameen
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引用次数: 0

Abstract

Oxazine and thiazine are heterocyclic organic compounds that have a wide range of pharmacological applications. In this study, some chalcone derivatives (1–5) were synthesized based on the reaction of an equal amount of p-substituted acetophenone and terephthalaldehyde in a basic medium. Oxazine derivatives (6-10) and thiazine derivatives (11–15) are synthesized from the reactions of chalcones (1-5) with urea and thiourea, respectively, in a basic medium. The newly synthesized compounds were identified using various physical techniques like 1H-NMR and FT-IR spectra, in addition to docking analysis for some of these derivatives. Finally, these compounds were tested for their biological activity, IC50, and % of PC3 cell line viability as markers of anticancer activity.
一种新的双恶嗪和噻嗪衍生物的合成及其生物活性研究
恶嗪和噻嗪是具有广泛药理应用的杂环有机化合物。本研究以等量的对苯乙酮和对苯二醛在碱性介质中反应合成了一些查尔酮衍生物(1-5)。查尔酮(1-5)在碱性介质中分别与尿素和硫脲反应合成了恶嗪衍生物(6-10)和噻嗪衍生物(11-15)。新合成的化合物使用各种物理技术,如1H-NMR和FT-IR光谱,除了对接分析这些衍生物的一些。最后,测试了这些化合物的生物活性、IC50和PC3细胞系存活率,作为抗癌活性的标志。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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