Rational design, synthesis, and anticancer evaluation of amide derivatives of Pyridin3-yl)imidazo[2,1-b][1,3,4]thiadiazole linked 1,3,4-oxadiazoles

IF 2.218 Q2 Chemistry Chemical Data Collections Pub Date : 2024-06-02 DOI:10.1016/j.cdc.2024.101147
Khasim Saheb Shaik , Saritha N , Nagendra Reddy G
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Abstract

A new series of amides of pyridin-3-yl)imidazo[2,1-b][1,3,4]thiadiazoles (13a-j) have been developed and confirmed by 1HNMR, 13CNMR and mass spectral data. Further, in the vitro anticancer activity of newly prepared compounds 13a-j was examined against four human cancer cell lines including MCF-7 & MDA MB-231 (human breast cancer), A549 (human lung cancer) and DU-145 (human prostate cancer) by employing the MTT assay, and using etoposide as a standard reference. These results indicated that the most of the derivatives displayed excellent to moderate anticancer activity. Among the five compounds 13a, 13b, 13c, 13d and 13e demonstrated remarkable activity as standard. One of the compounds 13a displayed excellent activity.

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吡啶-3-基)咪唑并[2,1-b][1,3,4]噻二唑与 1,3,4-恶二唑连接的酰胺衍生物的合理设计、合成和抗癌评估
研究人员开发了一系列新的吡啶-3-基)咪唑并[2,1-b][1,3,4]噻二唑酰胺类化合物(13a-j),并通过 1HNMR、13CNMR 和质谱数据进行了证实。此外,以依托泊苷为标准参照物,采用 MTT 法检测了新制备的 13a-j 化合物对四种人类癌细胞系(包括 MCF-7 &、MDA MB-231(人类乳腺癌)、A549(人类肺癌)和 DU-145(人类前列腺癌))的体外抗癌活性。这些结果表明,大多数衍生物都显示出了极佳至中等程度的抗癌活性。在五种化合物中,13a、13b、13c、13d 和 13e 具有显著的标准活性。其中一个化合物 13a 表现出了极佳的活性。
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Chemical Data Collections
Chemical Data Collections Chemistry-Chemistry (all)
CiteScore
6.10
自引率
0.00%
发文量
169
审稿时长
24 days
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