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Bioorg Med Chem Lett. 2011 Aug 15;21(16):4768-72. doi: 10.1016/j.bmcl.2011.06.073. Epub 2011 Jun 23.
Promising synthetic derivatives of macrolactone natural product (-)-A26771B have been designed and synthesized both from semisynthesis and total synthesis. Further optimization led to the first synthesis of macrolactam analogs of (-)-A26771B with improved antibacterial activity and metabolic stability.
已设计并合成了大环内酯天然产物(-)-A26771B 的有前途的合成衍生物,包括半合成和全合成。进一步优化导致了(-)-A26771B 的大环内酰胺类似物的首次合成,这些类似物具有改善的抗菌活性和代谢稳定性。