Abstract
Of the thousands of known chemical reactions, a handful of reactions, called “click” reactions, stand out with features such as good chemoselectivity, good solvent compatibilities, modularity, minimum synthetic demands, bioorthogonality and high yields. Among them, the Cu(I)-catalyzed 1,3-dipolar cycloaddition reaction between azides and terminal alkynes has emerged as a powerful tool in chemical biology and proteomics. This perspective surveys the significant contributions of click chemistry in catalomics (a sub-area in chemical proteomics), with special emphasis on activity-based protein profiling (ABPP), posttranslational modifications (PTMs) and enzyme inhibitor developments.
| Original language | English |
|---|---|
| Pages (from-to) | 1749-1762 |
| Number of pages | 14 |
| Journal | Organic & Biomolecular Chemistry |
| Volume | 8 |
| DOIs | |
| Publication status | Published - 11 Feb 2010 |
| Externally published | Yes |
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