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OGA inhibition by GlcNAc-selenazoline
The title compound, which differs from the powerful O-GlcNAcase (OGA) inhibitor GlcNAc-thiazoline only at the chalcogen atom (Se for S), is a much weaker inhibitor in a direct OGA assay. In human cells, however, the selenazoline shows comparable ability to induce hyper-O-GlcNAc-ylation, and the two...
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| Glavni autori: | , , , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2010
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4210863/ https://ncbi.nlm.nih.gov/pubmed/20822912 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bmc.2010.08.010 |
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