一类新型硫代海因衍生物的合成、表征及其抗前列腺癌和微生物活性研究。

Qusay Hays, None Dakhil Zughayir Mutlaq
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引用次数: 0

摘要

前列腺癌是男性最常见的恶性疾病之一,设计抗前列腺癌的新化合物是现代医学面临的挑战之一。本研究通过马来酰亚胺衍生物(1C-4)与异硫氰酸环己基反应,制备并表征了一系列新的硫代海因衍生物。用FT-IR、1H-NMR、13C-NMR对化合物进行了鉴定。采用MTT法测定制备的化合物对前列腺癌细胞系的活性,数据显示,基于IC50值,制备的化合物不具有抗前列腺癌活性。并对所制备的化合物对选定的细菌和真菌进行了抑菌活性研究,数据表明,所制备的系列化合物部分具有抗菌和抑菌活性,其中化合物4C具有较高的抗葡萄球菌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis, characterization of a new series of thiohydantoin derivatives and study their biological activity against prostate cancer and microbes.
Prostate cancer is one of the most common malignant diseases in men, and the design of new chemical compounds against prostate cancer is one of the challenges faced by modern medicine. In this study, we prepared and characterized a new series of thiohydantoin derivatives by reacting maleimide derivatives (1C-4) with cyclohexyl isothiocyanate.The prepared compounds were diagnosed using (FT-IR ,1H-NMR ,13C-NMR ).MTT assay was used to determine the activity of the prepared compounds against prostate cancer cell lines, as the data indicated, based on IC50 values, that the prepared compounds do not have anti-prostate cancer activity. The prepared compounds were also studied against selected types of bacteria and fungi, as the data indicated that some of the prepared series compounds had anti-bacterial and anti-fungal activity under study, as the compound 4C showed a high anti-staph activity.
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