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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >4'-Alkoxyl substitution enhancing the anti-mitotic effect of 5-(3',4',5'-substituted)anilino-4-hydroxy-8-nitroquinazolines as a novel class of anti-microtubule agents.
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4'-Alkoxyl substitution enhancing the anti-mitotic effect of 5-(3',4',5'-substituted)anilino-4-hydroxy-8-nitroquinazolines as a novel class of anti-microtubule agents.

机译:4'-烷氧基取代增强了5-(3',4',5'-取代)苯胺基-4-羟基-8-硝基喹唑啉的抗有丝分裂作用,这是一类新型的抗微管剂。

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摘要

Mitosis inhibitors are powerful anticancer drugs. Based on a novel anti-microtubule agent of 5-(4'-methoxy)anilino-4-hydroxy-8-nitroquinazoline, a series of 5-(3',4',5'-substituted)anilino-4-hydroxy-8- nitroquinazolines were designed and synthesized to investigate the effect of the substitution on the inhibitory activity against mitotic progression of tumor cells. The large alkoxyl substitution on the 4'-position of 5-anilino ring is beneficial for the potency. The 5-(3',4',5'-trimethoxy)anilino-8-nitroquinazoline (1h) displays an overwhelming activity in arresting the cells at the G2/M phase, providing a promising new template for further development of potent microtubule-targeted anti-mitotic drugs.
机译:有丝分裂抑制剂是有效的抗癌药。基于5-(4'-甲氧基)苯胺基-4-羟基-8-硝基喹唑啉的新型抗微管剂,一系列5-(3',4',5'-取代)苯胺基-4-羟基-设计并合成了8-硝基喹唑啉,以研究取代对肿瘤细胞有丝分裂进程抑制活性的影响。在5-苯胺基环的4'-位上的大量烷氧基取代有利于效力。 5-(3',4',5'-三甲氧基)苯胺基-8-硝基喹唑啉(1h)在将细胞阻滞于G2 / M期时表现出压倒性的活性,为进一步开发有效的微管提供了有希望的新模板。靶向抗有丝分裂药物。

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