American Chemical Society
Browse
ml9b00688_si_001.pdf (894.1 kB)

Brain Permeable Tafamidis Amide Analogs for Stabilizing TTR and Reducing APP Cleavage

Download (894.1 kB)
journal contribution
posted on 2020-03-12, 16:34 authored by Anjana Sinha, Jerry C. Chang, Peng Xu, Katherina Gindinova, Younhee Cho, Weilin Sun, Xianzhong Wu, Yue Ming Li, Paul Greengard, Jeffery W. Kelly, Subhash C. Sinha
Tafamidis, 1, a potent transthyretin kinetic stabilizer, weakly inhibits the γ-secretase enzyme in vitro. We have synthesized four amide derivatives of 1. These compounds reduce production of the Aβ peptide in N2a695 cells but do not inhibit the γ-secretase enzyme in cell-free assays. By performing fluorescence correlation spectroscopy, we have shown that TTR inhibits Aβ oligomerization and that addition of tafamidis or its amide derivative does not affect TTR’s ability to inhibit Aβ oligomerization. The piperazine amide derivative of tafamidis (1a) efficiently penetrates and accumulates in mouse brain and undergoes proteolysis under physiological conditions in mice to produce tafamidis.

History