Ruthenium polypyridyl complexes as inducer of ROS-mediated apoptosis in cancer cells by targeting thioredoxin reductase.
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Bypassing Mechanisms of Mitochondria-Mediated Cancer Stem Cells Resistance to Chemo- and RadiotherapyMetal- and Semimetal-Containing Inhibitors of Thioredoxin Reductase as Anticancer AgentsCUSP9* treatment protocol for recurrent glioblastoma: aprepitant, artesunate, auranofin, captopril, celecoxib, disulfiram, itraconazole, ritonavir, sertraline augmenting continuous low dose temozolomide.Ruthenium polypyridyl complex inhibits growth and metastasis of breast cancer cells by suppressing FAK signaling with enhancement of TRAIL-induced apoptosis.Ruthenium(II) Complexes with 2-Phenylimidazo[4,5-f][1,10]phenanthroline Derivatives that Strongly Combat Cisplatin-Resistant Tumor CellsRuthenium Complexes Induce HepG2 Human Hepatocellular Carcinoma Cell Apoptosis and Inhibit Cell Migration and Invasion through Regulation of the Nrf2 PathwayBiological processing of dinuclear ruthenium complexes in eukaryotic cells.Anticancer Activity Studies of Ruthenium(II) Complex Toward Human Osteosarcoma HOS Cells.The role of thioredoxin reductase 1 in melanoma metabolism and metastasis.A selenium-containing ruthenium complex as a cancer radiosensitizer, rational design and the important role of ROS-mediated signalling.The development of anticancer ruthenium(ii) complexes: from single molecule compounds to nanomaterials.Synthesis of Dipyridyl Ketone Isonicotinoyl Hydrazone Copper(II) Complex: Structure, Anticancer Activity and Anticancer Mechanism.Highly stable selenadiazole derivatives induce bladder cancer cell apoptosis and inhibit cell migration and invasion through the activation of ROS-mediated signaling pathways.Rational Design of Ruthenium Complexes Containing 2,6-Bis(benzimidazolyl)pyridine Derivatives with Radiosensitization Activity by Enhancing p53 Activation.Polypyridylruthenium(II) complexes exert anti-schistosome activity and inhibit parasite acetylcholinesterases.Enhancement of Antiangiogenic Efficacy of Iron(II) Complex by Selenium Substitution.The development of ruthenium(ii) polypyridyl complexes and conjugates for in vitro cellular and in vivo applications.Monomeric and dimeric coordinatively saturated and substitutionally inert Ru(ii) polypyridyl complexes as anticancer drug candidates.Antiangiogenic ruthenium(ii) benzimidazole complexes, structure-based activation of distinct signaling pathways.Endosomes: guardians against [Ru(Phen)3]2+ photo-action in endothelial cells during in vivo pO2 detection?
P2860
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P2860
Ruthenium polypyridyl complexes as inducer of ROS-mediated apoptosis in cancer cells by targeting thioredoxin reductase.
description
2014 nî lūn-bûn
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2014年の論文
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年學術文章
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name
Ruthenium polypyridyl complexe ...... rgeting thioredoxin reductase.
@en
Ruthenium polypyridyl complexe ...... rgeting thioredoxin reductase.
@nl
type
label
Ruthenium polypyridyl complexe ...... rgeting thioredoxin reductase.
@en
Ruthenium polypyridyl complexe ...... rgeting thioredoxin reductase.
@nl
prefLabel
Ruthenium polypyridyl complexe ...... rgeting thioredoxin reductase.
@en
Ruthenium polypyridyl complexe ...... rgeting thioredoxin reductase.
@nl
P2093
P2860
P356
P1433
P1476
Ruthenium polypyridyl complexe ...... rgeting thioredoxin reductase.
@en
P2093
Haoqiang Lai
Lianling Yu
Sai-Ming Ngai
Tianfeng Chen
Wenjie Zheng
Zhennan Zhao
Zuandi Luo
P2860
P304
P356
10.1039/C4MT00044G
P50
P577
2014-08-01T00:00:00Z