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Synthesis and biological evaluation of a novel series of chalcones incorporated pyrazole moiety as anticancer and antimicrobial agents

机译:一系列新的查耳酮并入吡唑部分作为抗癌和抗菌剂的合成和生物学评价

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摘要

A newly synthesized series of chalcone derivatives containing pyrazole rings were synthesized and evaluated for their cytotoxic activities in vitro against several human cancer cell lines. Most of the prepared compounds showed potential cytotoxicity against human breast cancer cell lines MCF-7, HEPG-2, and HCT-116. Also the compounds were evaluated as antimicrobial agents. The three compounds 3, 4, and 5 were proved to be better anticancer agents than the positive standard doxorubicin with IC50 values (4.7, 4.4, and 3.9 μg/ml) against the same human cancer cell lines, whereas compounds 5 and 6 showed the most active antimicrobial compounds in comparison to the other chalcones.
机译:合成了一系列新的含吡唑环的查耳酮衍生物,并评估了它们对几种人类癌细胞系的体外细胞毒活性。大多数制备的化合物显示出对人乳腺癌细胞系MCF-7,HEPG-2和HCT-116的潜在细胞毒性。还将该化合物评价为抗微生物剂。三种化合物3、4和5被证明是比阳性标准阿霉素更好的抗癌药,对同一人类癌细胞系的IC50值分别为(4.7、4.4和3.9μg/ ml),而化合物5和6显示出与其他查耳酮相比,活性最高的抗菌化合物。

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