Article ID Journal Published Year Pages File Type
1365534 Bioorganic & Medicinal Chemistry Letters 2007 4 Pages PDF
Abstract

A novel glycosphingolipid, β-d-GalNAcp(1 → 4)[α-d- Fucp(1 → 3)]-β-d-GlcNAcp(1→)Cer (1), isolated from the marine sponge Aplysinella rhax, has a unique structure, with d-fucose and N-acetyl-d-galactosamine attached to a reducing-end N-acetyl-d-glucosamine through an α1 → 3 and β1 → 4 linkage, respectively. We synthesized glycolipid analogues carrying a 2-branched fatty alkyl residue or a 2-trimethylsilyl ethyl residue in place of ceramide (2 and 3), non-natural type trisaccharide analogue containing an l-fucose residue (4), and other analogues (5 and 6). Among these prepared compounds, 2 showed the most potent nitric oxide (NO) production inhibitory activity against LPS-activated J774.1 cells. In addition, their structure–activity relationships were established.

Graphical abstractA novel glycosphingolipid analogue β-d-GalNAcp(1-4)[α-d-Fucp(1-3)]-β-d-GlcNAcp(1-R) (2) and some non-natural type trisaccharide analogues were synthesized, and their ability to inhibit the nitric oxide release was also examined.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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