posted on 2006-10-27, 00:00authored byThomas M. Fyles, Chi-Wei Hu, Horace Luong
A simple synthesis of oligoesters from TBDMS-protected-β- and THP-protected-ω-hydroxycarboxylic
acids using a solid-phase synthesis protocol is reported. Procedures were optimized for the efficient
production of ion channel candidates in high purity with minimal purification. The product oligoesters
were evaluated for ion transport activity using a fluorescent dye/vesicle assay. Oligoesters produced by
this strategy show structure-dependent activity; the most active compounds are closely comparable to
previously known oligoesters, but are available at a fraction of the synthetic effort.