Glycosphingolipids have been shown to mediate, among other things, cell-cell interactions and immune responses. The role of glycosphingolipids in immunomodulation, via the CD1 family of antigen presenting proteins, is of particular interest to us as this family may be involved in diseases such as juvenile diabetes, cancer, and malaria. We have recently shown that strained heterocycles, such as 2-methyleneoxetanes and 1,5-dioxaspiro[3.2]hexanes, serve as straightforward and versatile templates for glycosphingolipid synthesis. Using new methodology proposed herein we will expand our scope to beta-lactone templates to achieve the same end with increased efficiency. Ultimately, we will be able to assess the structural effects of alpha- and beta-glycosylated derivatives of Asteriacerebroside D in immune system modulation via the CD1 pathway. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31AI054346-02
Application #
6944737
Study Section
Special Emphasis Panel (ZRG1-F05 (29))
Program Officer
Hernandez, Milton J
Project Start
2004-08-11
Project End
2007-08-10
Budget Start
2005-08-11
Budget End
2006-08-10
Support Year
2
Fiscal Year
2005
Total Cost
$31,688
Indirect Cost
Name
University of Connecticut
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
614209054
City
Storrs-Mansfield
State
CT
Country
United States
Zip Code
06269
Ndonye, Rachel M; Izmirian, Douglas P; Dunn, Matthew F et al. (2005) Synthesis and evaluation of sphinganine analogues of KRN7000 and OCH. J Org Chem 70:10260-70