Title
GPI membrane anchors: Synthesis and functional evaluation of aminoglucosyl phosphatidylinositol core analogs
Document Type
Article
Publication Date
7-23-1996
Abstract
Analogs of GPI membrane anchor precursors were prepared from chiral inositol 1 and evaluated as substrates in rodent and trypanosomal cell-free incubates. Di-octanoyl GlcNα-PI 5b was an efficient mannose acceptor whereas di-palmitoyl GlcNα-PI 5a was unexpectedly refractory. Di-octanoyl β-anomer 8 was mannosylated only under conditions that permitted acylation of the inositol residue.
Publication Source (Journal or Book title)
Bioorganic and Medicinal Chemistry Letters
First Page
1715
Last Page
1718
Recommended Citation
Ye, J., Doerrler, W., Lehrman, M., & Falck, J. (1996). GPI membrane anchors: Synthesis and functional evaluation of aminoglucosyl phosphatidylinositol core analogs. Bioorganic and Medicinal Chemistry Letters, 6 (14), 1715-1718. https://doi.org/10.1016/0960-894X(96)00306-X