Abstract
A novel spin trap containing an iodoacetamide group has been synthesized and then used to target polypeptides, i.e. glutathione and bovine serum albumin, by which the resulting covalently bonded bioconjugates exhibit great potential for the application of spin trapping of transient radicals in biological systems.
| Original language | English |
|---|---|
| Pages (from-to) | 4943-4945 |
| Number of pages | 3 |
| Journal | Chemical Communications |
| Issue number | 39 |
| DOIs | |
| State | Published - Oct 21 2005 |
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