[HTML][HTML] Glutathione transferases: substrates, inihibitors and pro-drugs in cancer and neurodegenerative diseases

N Allocati, M Masulli, C Di Ilio, L Federici - Oncogenesis, 2018 - nature.com
Glutathione transferase classical GSH conjugation activity plays a critical role in cellular
detoxification against xenobiotics and noxious compounds as well as against oxidative …

A golden future in medicinal inorganic chemistry: the promise of anticancer gold organometallic compounds

B Bertrand, A Casini - Dalton Transactions, 2014 - pubs.rsc.org
From wedding rings on fingers to stained glass windows, by way of Olympic medals, gold
has been highly prized for millennia. Nowadays, organometallic gold compounds occupy an …

New insights in Au-NHCs complexes as anticancer agents

M Porchia, M Pellei, M Marinelli, F Tisato… - European journal of …, 2018 - Elsevier
Within the research field of antitumor metal-based agents alternative to platinum drugs, gold
(I/III) coordination complexes have always been in the forefront due mainly to the familiarity …

Glutathione transferases: potential targets to overcome chemoresistance in solid tumors

M Pljesa-Ercegovac, A Savic-Radojevic… - International journal of …, 2018 - mdpi.com
Multifunctional enzymes glutathione transferases (GSTs) are involved in the development of
chemoresistance, thus representing a promising target for a novel approach in cancer …

[HTML][HTML] Enzyme inhibition by metal complexes: concepts, strategies and applications

KJ Kilpin, PJ Dyson - Chemical Science, 2013 - pubs.rsc.org
Metal complexes are increasingly being used to inhibit enzymes. The reasons for this
increased interest arise from the special features that metal complexes offer, eg the facile …

[HTML][HTML] Monocarbonyl curcumin analogues as potent inhibitors against human glutathione transferase p1-1

P Pantiora, V Furlan, D Matiadis, B Mavroidi… - Antioxidants, 2022 - mdpi.com
The isoenzyme of human glutathione transferase P1-1 (hGSTP1-1) is involved in multi-drug
resistance (MDR) mechanisms in numerous cancer cell lines. In the present study, the …

Gold (III) complexes for antitumor applications: An overview

B Bertrand, MRM Williams… - Chemistry–A European …, 2018 - Wiley Online Library
Gold (III) complexes have emerged as a versatile and effective class of metal‐based
anticancer agents. The development of various types of ligands capable of stabilizing the …

[HTML][HTML] Clinically used antirheumatic agent auranofin is a proteasomal deubiquitinase inhibitor and inhibits tumor growth

N Liu, X Li, H Huang, C Zhao, S Liao, C Yang, S Liu… - Oncotarget, 2014 - ncbi.nlm.nih.gov
Proteasomes are attractive emerging targets for anti-cancer therapies. Auranofin (Aur), a
gold-containing compound clinically used to treat rheumatic arthritis, was recently approved …

[HTML][HTML] Comprehensive chemical proteomics analyses reveal that the new TRi-1 and TRi-2 compounds are more specific thioredoxin reductase 1 inhibitors than …

P Sabatier, CM Beusch, R Gencheva, Q Cheng… - Redox Biology, 2021 - Elsevier
Anticancer drugs that target cellular antioxidant systems have recently attracted much
attention. Auranofin (AF) is currently evaluated in several clinical trials as an anticancer …

Mass spectrometry as a powerful tool to study therapeutic metallodrugs speciation mechanisms: Current frontiers and perspectives

M Wenzel, A Casini - Coordination Chemistry Reviews, 2017 - Elsevier
Metal-based compounds form a promising class of therapeutic agents, whose mechanisms
of action still need to be elucidated, and that are in general prone to undergo extensive …