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One-Pot Synthesis and Biological Evaluation of Arylpropenone Aminochalcone Conjugates as Potential Apoptotic Inducers

机译:作为潜在凋亡诱导剂的芳基丙酮氨基酮结合物的一锅合成和生物学评估

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摘要

A facile single pot strategy was developed to synthesize a library of 17 arylpropenone aminochalcone conjugates involv- ing two consecutive reactions, namely Michael addition and Claisen-Schmidt condensation. These conjugates were screened for their in vitro anti-proliferative potential against selected human cancer cell lines such as breast (MCF-7 and MDA-MB- 231), pancreatic (PANC-1) and colorectal (CaCO2) adenocarcino- ma cells. Among them, the conjugates 6 l and 6p exhibited good to moderate cytotoxicity with IC50 values ranging from 6.7 μM and 9.8 μM, respectively, against MCF-7. Furthermore, these conjugates were found to exhibit G0/G1 cell cycle arrest.
机译:制定了一种简便的单锅策略,以合成17个芳基丙酮氨基酮的库,涉及两种连续反应的偶联物,即Michael添加和Claisen-Schmidt凝结。 对这些结合物的体外抗增殖潜力进行了筛查,以针对乳腺癌(MCF-7和MDA-MB-231),胰腺(PANC-1)和结直肠癌(CACO2)腺癌-MA细胞等人类癌细胞系。 其中,偶联物6 L和6P表现出良好至中度的细胞毒性,IC50值分别为6.7μm和9.8μm,相对于MCF-7。 此外,发现这些结合物表现出G0/G1细胞周期停滞。

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