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2-amino and 2 '-aminocombretastatin derivatives as potent antimitotic agents

机译:2-氨基和2'-氨基combretastatin衍生物作为有效的抗有丝分裂剂

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摘要

A novel series of 2-amino and 2'-aminocombretastatin derivatives were synthesized and evaluated for antitumor activity. Several compounds had excellent antiproliferative activity as inhibitors of tubulin polymerization. Compounds 11, 20, and 21 with IC50 values of 1.6, 1.7, and 1.8 mu M, respectively, exhibited more potent inhibition of tubulin polymerization than colchicine and approximately as active as combretastatin A-4. They also displayed antiproliferative activity with an IC50 values ranging from 11 to 44 nM in a variety of human cell lines from different organs. Structure activity relationship information suggests that the NH2 substituent at the 2-position of either ring A or ring B in combretastatin molecular skeleton may play an important role in the bioactivity of this series of compounds.
机译:合成了一系列新颖的2-氨基和2'-氨基combretastatin衍生物,并评估了其抗肿瘤活性。几种化合物作为微管蛋白聚合的抑制剂具有出色的抗增殖活性。化合物11、20和21的IC50值分别为1.6、1.7和1.8μM,与秋水仙碱相比,它们对微管蛋白聚合的抑制作用更强,并且活性与康维他汀A-4差不多。他们还在来自不同器官的多种人类细胞系中显示出抗增殖活性,IC50值在11至44 nM之间。结构活性关系信息表明,康柏他汀分子骨架中环A或环B 2位的NH2取代基可能在该系列化合物的生物活性中起重要作用。

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