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. 2016 Apr 26;7:11312. doi: 10.1038/ncomms11312

Figure 3. Fluorosamine reduces the synthesis of CSPGs by astrocytes.

Figure 3

(a) Chemical structures for GlcNAc and its derivatives. (b) Western blots for chondroitin-4-sulfate (sidechains) and stub chondroitin-4-sulfate (core proteins) show a concentration-dependent decrease in total CSPG content with fluorosamine treatment. (c) Chemical structures of four derivatives of fluorosamine with various substitutions to carbon-1 and carbon-4. (d) The 1-hydroxy and 1-propanoic fluorosamine derivatives were effective at reducing CSPG synthesis, whereas the 4-methoxy and 1-hydroxy-4-chloro compounds were ineffective. The results are presented as an individual experiment that was conducted three times.