Please use this identifier to cite or link to this item: https://doi.org/10.1021/om200783r
Title: Acetal-functionalized RAPTA complexes for conjugation and labeling
Authors: Tan, Y.Q.
Dyson, P.J.
Ang, W.H. 
Issue Date: 14-Nov-2011
Citation: Tan, Y.Q., Dyson, P.J., Ang, W.H. (2011-11-14). Acetal-functionalized RAPTA complexes for conjugation and labeling. Organometallics 30 (21) : 5965-5971. ScholarBank@NUS Repository. https://doi.org/10.1021/om200783r
Abstract: Ruthenium-arene complexes bearing the 1,3,5-triaza-7-phosphatricyclo-[3.3. 1.1]decane ligand, namely, RAPTA compounds, are widely investigated as potential antimetastatic agents for cancer therapy. Although much evidence points toward covalent binding with essential protein biomolecules as the key determinant of their activity, the exact biological targets of RAPTA remain elusive. To address this current gap in understanding, RAPTA compounds derivatized with acetal groups via a pendant chain to the arene ligand were developed as a functional probe for selective postlabeling and tagging of covalent RAPTA adducts in cancer cells. © 2011 American Chemical Society.
Source Title: Organometallics
URI: http://scholarbank.nus.edu.sg/handle/10635/75515
ISSN: 02767333
DOI: 10.1021/om200783r
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