Synthetic Progress of Fusarisetin A

Synthetic Progress of Fusarisetin A
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镰刀菌素A的合成进展

DOI:
10.6023/cjoc201210027
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发表时间:
2013
影响因子:
1.9
通讯作者:
Gao Shuanhu
Gao Shuanhu
中科院分区:
化学3区
文献类型:
--
作者:
Yin Jun;Kong Lili;Gao Shuanhu

文献摘要

被引文献

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Fusarisetin A是一种新的特特拉姆酸型天然产物,含有一个6-6-5-5-5稠合五环和10个立体中心。镰孢菌素A显示出对腺泡形态发生以及细胞迁移和侵袭的显著抑制,并显示出选择性抑制癌细胞转移的效力。本文综述了镰孢菌素A自发现以来的合成进展。
Fusarisetin A, a new tetramic acid type natural product, contains a 6-6-5-5-5 fused pentacycles and ten stereo-centers. Fusarisetin A displays significant inhibition of acinar morphogenesis as well as cell migration and invasion, and shows the potency for selective inhibition of cancer cell metastasis. This review summarizes the synthetic progress of fusarisetin A since its discovery.