A new target for gold (I) compounds: glutathione-S-transferase inhibition by auranofin

A De Luca, CG Hartinger, PJ Dyson, ML Bello… - Journal of Inorganic …, 2013 - Elsevier
… mechanisms of action of auranofin and analogues are still controversial. Here, we report on
the inhibition effects of glutathione S-transferase P1-1 (GST P1-1) exerted by auranofin. The …

Molecular mechanisms and clinical implications of the gold drug auranofin

S Shen, J Shen, Z Luo, F Wang, J Min - Coordination Chemistry Reviews, 2023 - Elsevier
… -based anti-inflammatory compound used for the treatment of … focus mainly on its inhibitory
effects on antioxidant defensive … to the identification of a variety of targets for AUR, and this …

Thioredoxin reductase: A target for gold compounds acting as potential anticancer drugs

A Bindoli, MP Rigobello, G Scutari, C Gabbiani… - Coordination Chemistry …, 2009 - Elsevier
… by gold compounds are mainly the result of potent inhibition of … The antiarthritic gold(I)
phosphine drug, auranofin, was … (PDI), glutathione S-transferase and Escherichia coli DsbA, …

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
Auranofin is an antiarthritic gold phosphine compound that … in contrast to other described
targets 103 . Therefore, future … mechanism of enzyme inhibition played by auranofin on GSTs…

Toward anticancer gold-based compounds targeting PARP-1: a new case study

A Citta, V Scalcon, P Göbel, B Bertrand, M Wenzel… - RSC …, 2016 - pubs.rsc.org
… (GR), glutathione-S-transferase, 12 cysteine proteases, 13 … shown to be potently inhibited
by gold complexes. Interestingly, … and cell extracts, in comparison to auranofin, the gold(I) anti-…

Dual targeting of the thioredoxin and glutathione systems in cancer and HIV

M Benhar, IL Shytaj, JS Stamler… - The Journal of clinical …, 2016 - Am Soc Clin Investig
… selectively targeted by Trx and GSH inhibitors. Trx and GSH … Conversely, the TrxR inhibitor
auranofin partially inhibits the … compounds, likely via S-nitrosylation (71, 72). Additionally, …

Cystatin SN inhibits auranofin-induced cell death by autophagic induction and ROS regulation via glutathione reductase activity in colorectal cancer

BM Oh, SJ Lee, HJ Cho, YS Park, JT Kim… - Cell death & …, 2017 - nature.com
… represent a potential target for colorectal cancer therapy. … -NT substrate and Glutathione
S-Transferase) added to each well of … inhibitor auranofin and aldehyde dehydrogenase inhibitor

A soluble bis-chelated gold (I) diphosphine compound with strong anticancer activity and low toxicity

Y Wang, M Liu, R Cao, W Zhang, M Yin… - Journal of Medicinal …, 2013 - ACS Publications
… be their therapeutic targets. For example, auranofin was reported to strongly inhibit two Sec-…
(17, 18) Auranofin was also shown to possess only modest inhibitory effect on glutathione …

New Class of Anti-Inflammatory Therapeutics Based on Gold (III) Complexes in Intestinal Inflammation–Proof of Concept Based on In Vitro and In Vivo Studies

JB Krajewska, J Włodarczyk, D Jacenik… - International Journal of …, 2021 - mdpi.com
… , cysteine protease, and glutathione-S-transferase, and therefore cause … However, auranofin,
a gold(I)-containing compoundAuranofin inhibited Clostridium difficile toxin production and …

[PDF][PDF] DISCOVERY OF APPROVED DRUGS WITH POSSIBLE MULTI-TARGET INHIBITORY ACTIVITIES AGAINST SCHISTOSOMA SPECIES

FC EZEBUO - 2018 - phd-dissertations.unizik.edu.ng
… reference compounds (praziquantel, oxamniquine, auranofin … Schistosomal glutathione
s-transferase and sulfotransferase … In (D) yellow spheres are gold molecules from auranofin in …