| Literature DB >> 33062181 |
Anjana Sinha1, Jerry C Chang1,2, Peng Xu1, Katherina Gindinova1, Younhee Cho3, Weilin Sun1, Xianzhong Wu2, Yue Ming Li2, Paul Greengard1, Jeffery W Kelly3, Subhash C Sinha1.
Abstract
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.Entities:
Year: 2020 PMID: 33062181 PMCID: PMC7549266 DOI: 10.1021/acsmedchemlett.9b00688
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345