| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 8209863 | Applied Radiation and Isotopes | 2015 | 5 Pages | 
Abstract
												In this work a new coupling reagent, N-[2-(maleimido)ethyl]-3-(trimethylstannyl)benzamide, for radiohalogenation has been synthesized and characterized. The reagent is intended to either be attached to reduced disulfide bridges of proteins (making the halogenation site-specific) or to free terminal cysteine groups on peptides. The new reagent was also shown to be easily halogenated with inactive bromine and iodine as well as 125I and 211At, indicating potential use within targeted radiotherapy.
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											Authors
												Emma Aneheim, Mark R. StJ. Foreman, Holger Jensen, Sture Lindegren, 
											![First Page Preview: N-[2-(maleimido)ethyl]-3-(trimethylstannyl)benzamide, a molecule for radiohalogenation of proteins and peptides N-[2-(maleimido)ethyl]-3-(trimethylstannyl)benzamide, a molecule for radiohalogenation of proteins and peptides](/preview/png/8209863.png)