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Synthesis of macrosphelides with a thiazole side chain: New antitumor candidates having apoptosis-inducing property

机译:具有噻唑侧链的大肽的合成:具有诱导细胞凋亡特性的新型抗肿瘤药物

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摘要

Hybrid compounds of macrosphelides and epothilones, both of which are natural macrolides having a 16-membered skeleton, were designed and synthesized using a ring-closing metathesis (RCM) strategy. Some of these hybrids were found to exhibit notable apoptosis-inducing activity against human lymphoma cells with higher potency than parent natural macrosphelides, and to be a promising lead compound for development of a new antitumor agent.
机译:使用闭环复分解(RCM)策略设计和合成了大环内酯和埃博霉素的杂合化合物,两者均为具有16元骨架的天然大环内酯。发现这些杂种中的一些杂种对人淋巴瘤细胞表现出显着的凋亡诱导活性,并且比亲本天然大环糊精具有更高的效力,并且是开发新的抗肿瘤剂的有希望的先导化合物。

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