Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.bioorg.2007.12.004
DC FieldValue
dc.titleDivergent syntheses of all stereoisomers of phytosphingosine and their use in the construction of a ceramide library
dc.contributor.authorPark, J.-J.
dc.contributor.authorLee, J.H.
dc.contributor.authorLi, Q.
dc.contributor.authorDiaz, K.
dc.contributor.authorChang, Y.-T.
dc.contributor.authorChung, S.-K.
dc.date.accessioned2014-06-23T05:37:04Z
dc.date.available2014-06-23T05:37:04Z
dc.date.issued2008-10
dc.identifier.citationPark, 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
dc.identifier.issn00452068
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75979
dc.description.abstractSphingolipids 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.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.bioorg.2007.12.004
dc.sourceScopus
dc.subjectApoptosis
dc.subjectCeramide
dc.subjectInflammatory response
dc.subjectLibrary
dc.subjectPhytosphingosine
dc.subjectSolid phase acylating reagent
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1016/j.bioorg.2007.12.004
dc.description.sourcetitleBioorganic Chemistry
dc.description.volume36
dc.description.issue5
dc.description.page220-228
dc.description.codenBOCMB
dc.identifier.isiut000261905800007
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