申请人:Demchenko Alexei
公开号:US20140066390A1
公开(公告)日:2014-03-06
The invention provides a series of novel Lipid A anlogues that are structually simple, synthetically accessible, and capable of blocking the cellular receptor within the signal transduction pathway. The novel Lipid A anlogues can include a monosaccharide core with hydrophobic side chains and amino acid ionic motif. The invention further provides methods of using the compounds and compositions thereof in various therapeutic methods.
本发明提供了一系列新颖的脂多糖A类似物,这些类似物结构简单、合成容易,并能够阻断信号转导通路内的细胞受体。这些新颖的脂多糖A类似物可以包括具有疏水侧链和氨基酸离子基团的单糖核心。本发明还提供了使用这些化合物及其组合物进行各种治疗方法的方法。