Suppr超能文献

新型双吲哚啉酮衍生物的合成及细胞毒性评价。

Synthesis and Biological Evaluation of New Bis-Indolinone Derivatives Endowed with Cytotoxic Activity.

机构信息

Department of Pharmacy and Biotechnology, Alma Mater Studiorum-University of Bologna, Via Belmeloro 6, 40126 Bologna, Italy.

Department for Life Quality Studies, Alma Mater Studiorum-University of Bologna, Corso d'Augusto 237, 47921 Rimini, Italy.

出版信息

Molecules. 2021 Oct 16;26(20):6277. doi: 10.3390/molecules26206277.

Abstract

A series of new Knoevenagel adducts, bearing two indolinone systems, has been synthesized and evaluated on 60 human cancer cell lines according to protocols available at the National Cancer Institute (Bethesda, MD, USA). Some derivatives proved to be potent antiproliferative agents, showing GI values in the submicromolar range. Compound emerged as the most active and was further studied in Jurkat cells in order to determine the effects on cell-cycle phases and the kind of cell death induced. Finally, oxidative stress and DNA damage induced by compound were also analyzed.

摘要

已经合成了一系列带有两个吲哚啉酮系统的新型 Knoevenagel 加合物,并根据美国国立癌症研究所(马里兰州贝塞斯达)提供的方案对 60 个人类癌细胞系进行了评估。一些衍生物被证明是有效的增殖抑制剂,其 GI 值在亚微摩尔范围内。化合物 表现出最强的活性,并在 Jurkat 细胞中进一步研究,以确定对细胞周期各阶段的影响以及诱导的细胞死亡类型。最后,还分析了化合物 引起的氧化应激和 DNA 损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eeb/8537952/fa345600f9d4/molecules-26-06277-sch001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验