An efficient conjugation method between hydrophilic and hydrophobic components using a solid-phase assisted disulfide ligation.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION(2018)

引用 7|浏览8
暂无评分
摘要
Chemical conjugation between hydrophilic and hydrophobic components is difficult because of their extremely different solubility. Herein, we report a new versatile method with a solid-phase-assisted disulfide ligation to overcome the difficulty of conjugation attributed to solubility. The method involves two steps in a one-pot process: 1)loading of a hydrophobic molecule onto a resin in an organic solvent, and 2)release of the solid-supported hydrophobic molecule as a conjugate with a hydrophilic molecule into an aqueous solvent. This strategy allows the use of a suitable solvent system for the substrates in each step. Conjugates of a water-insoluble drug, plinabulin, with hydrophilic carriers that could not be prepared by solution-phase reactions were obtained in moderate yields (29-45%). This strategy is widely applicable to the conjugation of compounds with solubility problems.
更多
查看译文
关键词
peptide-drug conjugate,solid-phase synthesis,solubility,synthetic methods
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要