Please use this identifier to cite or link to this item:
|Title:||Divergent syntheses of all stereoisomers of phytosphingosine and their use in the construction of a ceramide library|
Solid phase acylating reagent
|Citation:||Park, J.-J., Lee, J.H., Li, Q., Diaz, K., Chang, Y.-T., Chung, S.-K. (2008-10). Divergent syntheses of all stereoisomers of phytosphingosine and their use in the construction of a ceramide library. Bioorganic Chemistry 36 (5) : 220-228. ScholarBank@NUS Repository. https://doi.org/10.1016/j.bioorg.2007.12.004|
|Abstract:||Sphingolipids such as ceramide and sphingosine-1-phosphate have recently attracted intense research interests because of their functional roles as signaling molecules in many important physiological processes, such as growth arrest, apoptosis, and inflammatory responses, and cell proliferation, vascular maturation and trafficking of lymphocytes. The well-defined modular structures of ceramides and related glycosylceramides are ideally amenable to library formation for medicinal chemistry investigation. We have developed divergent synthetic routes to all eight phytosphingosine stereoisomers and then proceeded to prepare phytosphingosine-based ceramide library composed of more than 500 compounds. © 2008 Elsevier Inc. All rights reserved.|
|Source Title:||Bioorganic Chemistry|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on May 20, 2018
WEB OF SCIENCETM
checked on Apr 23, 2018
checked on Apr 20, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.