Benzoxazoles as transthyretin amyloid fibril inhibitors: Synthesis, evaluation, and mechanism of action

被引:211
作者
Razavi, H
Palaninathan, SK
Powers, ET
Wiseman, RL
Purkey, HE
Mohamedmohaideen, NN
Deechongkit, S
Chiang, KP
Dendle, MTA
Sacchettini, JC
Kelly, JW [1 ]
机构
[1] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[3] Texas A&M Univ, Dept Biochem & Biophys, College Stn, TX 77843 USA
关键词
aggregation; bioorganic chemistry; drug design; inhibitors; structure-activity relationships;
D O I
10.1002/anie.200351179
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Benzoxazoles pevent misfolding: Benzoxazole-based inhibitors of transthyretin (TTR) amyloid fibril formation are among the most effective found to date. They stabilize TTR against both acid-mediated misfolding and urea denaturation by raising the activation barrier to tetramer dissociation, the rate-limiting step for amyloid formation. The figure depicts the cocrystal structure of one of the better benzoxazole inhibitors bound to TTR.
引用
收藏
页码:2758 / 2761
页数:4
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