Fabry Disease (FD) is a rare lysosomal storage disorder characterized by α-galactosidase A (α-Gal A) enzyme deficiency, resulting in glycosphingolipid accumulation. Its clinical spectrum ranges from severe classical...
The Ministry of Science and Technology of the People’s Republic of China[2016ZX09101017]supported this project.
Ganglioside and sulfatide are primary components of acidic glycosphingolipids(AGSLs),which are abundant in the brain tissue.AGSLs are potential tumor markers.In this paper,we use ultra-high performance liquid chromato...
An efficient and practical route to synthesize (2S,3S,4R)-2-azido-3,4-O-isopropyllidene-1,3,4-octadecanetriol from D-galactose in 18% overall yield was described, which required ten steps of reactions and only four ...