Synthesis of novel unsymmetrical alkyl-aryl-selenides: β-carbonyl-selenides derivatives and anticancer evaluation

As a new kind of unsymmetrical alkyl-aryl-selenides, a series of novel β-carbonyl-selenides derivatives were synthesized with high regioselectivity and substrates tolerance. Total six series and forty-four compounds were generated. The in vitro antiproliferative activities were evaluated on U251-MG,...

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Veröffentlicht in:Chemical papers 2022-09, Vol.76 (9), p.5471-5485
Hauptverfasser: Feng, Shuxiao, Qi, Kaiyan, Ma, Junying, Guo, Yafei, Gao, Jiayu, Liu, Pu, Wang, Junling, Gu, Guangna, Dong, Le, Wang, Jinhua, Li, Wan, Yang, Yihui, Du, Guanhua, Qu, Lingbo, Zhang, Shouren
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Sprache:eng
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Zusammenfassung:As a new kind of unsymmetrical alkyl-aryl-selenides, a series of novel β-carbonyl-selenides derivatives were synthesized with high regioselectivity and substrates tolerance. Total six series and forty-four compounds were generated. The in vitro antiproliferative activities were evaluated on U251-MG, U87-MG, MDA-MB-231, HCT116 and SW620 cells lines. Structure and antiproliferative relationship were discussed. Among them, (±)-N, N′-(1,2-phenylene)-bis-(2-((3-oxobutan-2-yl)selanyl) benzamide) ( 5t ) has significant antiproliferative activity and potential value as anticancer agent with IC 50 values  86.36 µM in test tumor cells.
ISSN:0366-6352
1336-9075
2585-7290
DOI:10.1007/s11696-022-02164-6