Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5274629 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
The cationic (η6-arene)ruthenium complexes 6–9 containing a chloroacetamide or a maleimide functional group on the arene ligand were synthesized and successfully used to introduce ruthenium(II) species to the active site of the cysteine endoproteinase papain in a site-directed and covalent fashion as shown by enzymatic and ESI-MS studies.
Graphical abstractChloroacetamide and maleimide derivatives of cationic (η6-arene)ruthenium complexes were synthesized and anchored to the active site of the cysteine endoproteinase papain in a site-directed and covalent fashion.Figure optionsDownload full-size imageDownload as PowerPoint slide
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