作者:Lei Chen、Kausar Begam Riaz Ahmed、Peng Huang、Zhendong Jin
DOI:10.1002/anie.201209300
日期:2013.3.18
By design: A truncated superstolide A, a simplified analogue of the potent anticancer marine macrolide superstolide A, was designed and successfully synthesized by a highly efficient and convergent approach. The biological evaluation showed that this compound maintains the potent anticancer activity of the original natural product superstolide A.
通过设计:截短的 superstolide A,一种有效的抗癌海洋大环内酯 superstolide A 的简化类似物,是通过高效和收敛的方法设计并成功合成的。生物学评估表明,该化合物保持了原始天然产物 superstolide A 的有效抗癌活性。