Matsuya Yuji, Kawaguchi Takanori, Ishihara Kentaro, Ahmed Kanwal, Zhao Qing-Li, Kondo Takashi, Nemoto Hideo
Faculty of Pharmaceutical Sciences, and Department of Radiological Sciences, Faculty of Medicine, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan.
Org Lett. 2006 Sep 28;8(20):4609-12. doi: 10.1021/ol061922v.
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.
大环球霉素和埃坡霉素均为具有16元骨架的天然大环内酯类化合物,利用关环复分解(RCM)策略设计并合成了它们的杂合化合物。发现其中一些杂合化合物对人淋巴瘤细胞表现出显著的凋亡诱导活性,其效力高于母体天然大环球霉素,有望成为开发新型抗肿瘤药物的先导化合物。