一些芳基酮肟衍生物的合成及其体外抑菌和细胞毒活性

O. Karaosmanoğlu, Burcu Butun, H. Dal, Hülya Sivas, K. Benkli
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引用次数: 1

摘要

苯并呋喃衍生物存在于几种天然化合物中,可用于各种用途。由于其分子结构的电子行为,它们具有抗肿瘤、细胞毒性、抗癌、抗微生物、抗真菌、抗蚂蚁等多种生物活性。我们合成了(3-甲基-苯并呋喃-2-基)酮肟衍生物(其中一种是新化合物),并用IR、1H-NMR、MASS光谱和元素分析对这些化合物进行了结构鉴定。文献中首次阐明了H2化合物的X射线分析。还首次通过MTT和NR摄取法评估了对F2408和HepG2细胞系的细胞毒性活性。用肉汤微稀释试验研究了H1、H2和H3的抗菌活性。结果表明,这些酮肟在不同的高剂量下具有细胞毒性和抗微生物活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of Some Aryl Ketoxime Derivatives with their in vitro Anti-microbial and Cytotoxic Activity
Benzofuwran derivatives found in several natural compounds and synthesized for various purposes. Due to their molecular structure’s electron behaviors they have several biological activities such as antitumor, cytotoxic, anticancer, antimicrobial, antifungal, ant proliferative etc. We synthesized (3-methyl-benzofuran-2-yl) ketoxime derivatives (one of them are new compound) and structure elucidation of the compounds was performed using IR, 1H-NMR, MASS spectroscopy and elemental analysis. X-Ray analysis of H2 compound was elucidated for the first time with this study in the literature. Cytotoxic activity against F2408 and HepG2 cell lines was also evaluated for the first time by MTT and NR uptake methods. Anti-microbial activity of H1, H2 and H3 was also investigated with broth micro dilution test. The results show that these ketoximes have cytotoxic and anti-microbial activity on different higher doses.
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