Design, Synthesis and Structural Characterization of Novel Thioanthraquinone Analogues from 1,5-Dichloroanthraquinone

Funda Özkök
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Abstract

Anthraquinone and its derivatives are considered intermediate agents with superior properties due to their activities in chemical and biological reaction. A new, economical, practical and one-step synthesis method was developed by our research team for the synthesis of amino and thioanthraquinones in previous studies (1). With this synthesis method, thioanthraquinone analogs 2(a-d) were obtained from 1,5-Dichloroanthraquinone (1) and bioactive thiols. The synthesized organic molecules were purified by column chromatography and their structures were identified with spectroscopic methods. Fluorescence analyzes of synthesized thioanthraquinone analogues were performed. It was determined that all thioanthraquinone analogues synthesized and characterized in the study showed fluorescence activity. These new analogues with fluorescence are expected to find application in drug delivery systems and sensor studies.
1,5-二氯蒽醌类新型硫代蒽醌类似物的设计、合成及结构表征
蒽醌及其衍生物因其在化学和生物反应中的活性而被认为是性能优越的中间体。本课题组在前期研究中开发了一种新的、经济实用的一步合成氨基蒽醌和硫代蒽醌的方法(1)。该合成方法从1,5-二氯蒽醌(1)和生物活性硫醇中得到了硫代蒽醌类似物2(A -d)。用柱层析法对合成的有机分子进行了纯化,并用波谱法对其结构进行了鉴定。对合成的硫代蒽醌类似物进行荧光分析。结果表明,本研究合成并表征的硫代蒽醌类似物均具有荧光活性。这些新的荧光类似物有望在药物输送系统和传感器研究中找到应用。
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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