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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Design, synthesis and discovery of 5-hydroxyaurone derivatives as growth inhibitors against HUVEC and some cancer cell lines.
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Design, synthesis and discovery of 5-hydroxyaurone derivatives as growth inhibitors against HUVEC and some cancer cell lines.

机译:设计,合成和发现5-羟基金莲花衍生物作为抗HUVEC和某些癌细胞系的生长抑制剂。

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摘要

A series of 4'-substituted 5-hydroxyaurone derivatives were synthesized and their inhibitory activities against the proliferation of endothelial cells and two cancer cell lines were studied. Some of these compounds functioned as potent inhibitors against the proliferation of endothelial cells and cancer cells but possessed much weaker cytotoxic activities against non-cancer cell line of CCC-HPF-1. It was demonstrated that two most active compounds 16 and 27 effectively inhibited in vitro endothelial cell motility and tube formation, which are basic properties of endothelial cells for angiogenesis. Moreover, 16 and 27 also showed significant activities against in vitro cancer cell invasion, indicating that they have potential to inhibit cancer metastasis. These composite results suggest that 4'-substituted 5-hydroxyaurone is indeed a candidate structural scaffold for anticancer agent targeting activated endothelial cells and fast-proliferating cancer cells.
机译:合成了一系列的4'-取代的5-羟基金龙酮衍生物,并研究了它们对内皮细胞和两种癌细胞系增殖的抑制作用。这些化合物中的一些作为有效的抑制剂来对抗内皮细胞和癌细胞的增殖,但对CCC-HPF-1的非癌细胞系具有弱得多的细胞毒性。已证明两种活性最高的化合物16和27有效抑制了体外内皮细胞的运动和管的形成,这是内皮细胞用于血管生成的基本特性。此外,16和27还显示出对体外癌细胞侵袭的显着活性,表明它们具有抑制癌症转移的潜力。这些综合结果表明,4'-取代的5-羟基金龙酮确实是靶向活化的内皮细胞和快速增殖的癌细胞的抗癌剂的候选结构支架。

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