Synthesis of 5-nitro-2-furancarbohydrazides and their cis-diamminedichloroplatinum complexes as bitopic and irreversible human thioredoxin reductase inhibitors

…, S Gromer, K Becker, E Davioud-Charvet

文献索引：Millet, Regis; Urig, Sabine; Jacob, Judit; Amtmann, Eberhard; Moulinoux, Jacques-Philippe; Gromer, Stephan; Becker, Katja; Davioud-Charvet, Elisabeth Journal of Medicinal Chemistry, 2005 , vol. 48, # 22 p. 7024 - 7039

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被引用次数: 35

摘要

The human selenoprotein thioredoxin reductase is involved in antioxidant defense and DNA synthesis. As increased thioredoxin reductase levels are associated with drug sensitivity to cisplatin and drug resistance in tumor cells, this enzyme represents a promising target for the development of cytostatic agents. To optimize the potential of the widely used cisplatin to inhibit the human thioredoxin reductase and therefore to overcome cisplatin resistance, ...