Rivkin Alexey, Yoshimura Fumihiko, Gabarda Ana E, Chou Ting-Chao, Dong Huajin, Tong William P, Danishefsky Samuel J
Laboratory for Bioorganic Chemistry, Sloan-Kettering Institute for Cancer Research, 1275 York Avenue, New York, New York 10021, USA.
J Am Chem Soc. 2003 Mar 12;125(10):2899-901. doi: 10.1021/ja029695p.
The total synthesis of a family of (E)-9,10-dehydro derivatives of epothilone D (i.e., 12,13-desoxyepothilone B) is described. The route is particularly concise and amenable to production of new congeners. Furthermore, the chemistry described herein constitutes a major simplification in the total synthesis of EpoD, which is in human clinical trials. This new family of epothilones shows major advantages in terms of their potency and pharmacostability relative to the wild-type saturated analogues in the D series. From the perspective of compound availability through synthesis, potency, and pharmacokinetic properties, these compounds could well warrant advancement to clinical evaluation in humans.
描述了埃坡霉素D的(E)-9,10-脱氢衍生物家族(即12,13-脱氧埃坡霉素B)的全合成。该路线特别简洁,适合生产新的同系物。此外,本文所述的化学方法在处于人体临床试验阶段的埃坡霉素D的全合成中实现了重大简化。相对于D系列中的野生型饱和类似物,这个新的埃坡霉素家族在效力和药物稳定性方面显示出主要优势。从通过合成获得化合物的可用性、效力和药代动力学性质的角度来看,这些化合物很可能值得推进到人体临床评估阶段。