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Synthesis and Anticancer Activity of Amide Derivatives of 1,2-Isoxazole Combined 1,2,4-Thiadiazole

机译:1,2-异恶唑的酰胺衍生物合成和抗癌活性组合1,2,4-噻二唑的衍生物

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摘要

A series of amide derivatives of 1,2-isoxazole combined with 1,2,4-thiadiazole are synthesized 11a-11j. Their chemical structures are confirmed by H-1 and C-13 NMR, and mass spectra. The products are tested for their anticancer activity against four types of human cancer cell lines, including MCF-7 (breast), A549 (lung), Colo-205 (colon), and A2780 (ovarian). Etoposide is used as a positive control. Most of the compounds show good anticancer activity. The compounds 11b, 11c, 11d, 11e, 11g, and 11j demonstrate more potent activity than etoposide.
机译:1,2-异恶唑的一系列酰胺衍生物与1,2,4-噻二唑结合的合成11A-11J。 它们的化学结构由H-1和C-13 NMR和质谱证实。 该产品经过针对四种类型的人癌细胞系进行抗癌活动,包括MCF-7(乳房),A549(肺),Colo-205(结肠)和A2780(卵巢)。 依托泊苷用作阳性对照。 大多数化合物都显示出良好的抗癌活动。 化合物11b,11c,11d,11e,11g和11j表现出比依托泊苷的更有效的活性。

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