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New naphthopyran analogues of LY290181 as potential tumor vascular-disrupting agents

机译:LY290181新的萘甲卓坦类似物作为潜在的肿瘤血管破坏剂

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摘要

A series of 19 analogues of the antiproliferative naphthopyran LY290181 were prepared for structure-activity relationship studies. We found the best activities for test compounds bearing small substituents at the meta position of the phenyl ring. The mode of action of LY290181 and eight new analogues was studied in detail. The compounds were highly anti-proliferative with IC50 values in the subnanomolar to triple-digit nanomolar range. The new analogues led to G2/M arrest due to interruption of the microtubule dynamics. In 518A2 melanoma cells they caused a mitotic catastrophe which eventually led to apoptosis. The naphthopyrans also induced a disruption of the vasculature in the chorioallantoic membrane (CAM) of fertilized chicken eggs as well as in xenograft tumors in mice. In a preliminary therapy trial, the difluoro derivative 2b retarded the growth of resistant xenograft tumors in mice. (C) 2018 Elsevier Masson SAS. All rights reserved.
机译:为结构活性关系研究制备了一系列19个抗增殖萘甲烷LY290181的类似物。 我们发现在苯环元位置轴承小取代基的测试化合物的最佳活性。 详细研究了LY290181和八种新类似物的作用方式。 将化合物高度抗增殖与亚甲醇中的IC 50值高到三位数纳米摩尔范围。 由于微管动态的中断,新的类似物导致G2 / M被逮捕。 在518A2黑色素瘤细胞中,它们引起了毒性灾难,最终导致细胞凋亡。 萘甲烷还诱导受精鸡蛋的血管基质膜(凸轮)中的脉管系统以及小鼠的异种移植肿瘤中断。 在初步治疗试验中,二氟衍生物2B延迟了小鼠抗性异种移植肿瘤的生长。 (c)2018年Elsevier Masson SAS。 版权所有。

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