Karaca, Özden, Scalcon, Valeria, Meier-Menches, Samuel M., Bonsignore, Riccardo ![]() ![]() |
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Official URL: http://dx.doi.org/10.1021/acs.inorgchem.7b02345
Abstract
The synthesis of novel hydrophilic gold(I) NHC complexes is reported. Selected compounds distinctly target the pivotal biological target thioredoxin reductase (TrxR) in the nanomolar range, as for the benchmark anticancer drug auranofin, and exhibit remarkable antiproliferative effects against human ovarian cancer cells.
Item Type: | Article |
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Date Type: | Published Online |
Status: | Published |
Schools: | Chemistry |
Publisher: | American Chemical Society |
ISSN: | 0020-1669 |
Date of First Compliant Deposit: | 14 November 2017 |
Date of Acceptance: | 2 November 2017 |
Last Modified: | 19 Nov 2024 21:45 |
URI: | https://orca.cardiff.ac.uk/id/eprint/106490 |
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