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Medicinal gold compounds form tight adducts with the copper chaperone Atox-1: Biological and pharmacological implications

Academic Article
Publication Date:
2012
abstract:
Based on ESI-MS measurements, we show here that some representative cytotoxic gold(iii) compounds produce stable adducts upon reaction with the copper chaperone Atox-1; notably, such adducts contain gold in the oxidation state +1. These findings are of interest to understand the intracellular metabolism of medicinal gold species and to develop new potent inhibitors of the copper trafficking system.
Iris type:
01.01 Articolo in rivista
Keywords:
auranofin; chaperone; copper; gold derivative; protein Atox 1; unclassified drug; article; binding site; chemical reaction; complex formation; cytotoxicity; density functional theory; drug protein binding; drug stability; drug structure; electrospray mass spectrometry; oxidation
List of contributors:
Michelucci, Elena
Authors of the University:
MICHELUCCI ELENA
Handle:
https://iris.cnr.it/handle/20.500.14243/415831
Published in:
CHEMICAL COMMUNICATIONS (LOND., 1996, PRINT)
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https://www.scopus.com/inward/record.uri?eid=2-s2.0-84869014485&doi=10.1039%2fc2cc36610j&partnerID=40&md5=2c9d5fd34c0baaf31c256329ee95f3e7
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