Increasing intracellular bioavailable copper selectively targets prostate cancer cells.
about
Mechanistic characterization of a copper containing thiosemicarbazone with potent antitumor activity.Copper complexation screen reveals compounds with potent antibiotic properties against methicillin-resistant Staphylococcus aureus.Pharmacological activity of metal binding agents that alter copper bioavailability.Synthesis, DNA binding, cellular DNA lesion and cytotoxicity of a series of new benzimidazole-based Schiff base copper(II) complexes.Combinatorial phenotypic screen uncovers unrecognized family of extended thiourea inhibitors with copper-dependent anti-staphylococcal activity.Copper(II)-Bis(Thiosemicarbazonato) Complexes as Antibacterial Agents: Insights into Their Mode of Action and Potential as Therapeutics.Copper-64 Dichloride as Theranostic Agent for Glioblastoma Multiforme: A Preclinical Study.Doxorubicin Conjugated to Immunomodulatory Anticancer Lactoferrin Displays Improved Cytotoxicity Overcoming Prostate Cancer Chemo resistance and Inhibits Tumour Development in TRAMP MiceCopper as a target for prostate cancer therapeutics: copper-ionophore pharmacology and altering systemic copper distribution.Targeting copper in cancer therapy: 'Copper That Cancer'.Synthesis, X-ray structure and in vitro cytotoxicity studies of Cu(I/II) complexes of thiosemicarbazone: special emphasis on their interactions with DNA.A Role for The ATP7A Copper Transporter in Tumorigenesis and Cisplatin ResistanceInhibition of respiratory complex I by copper(ii)-bis(thiosemicarbazonato) complexes.Heterogeneous copper concentrations in cancerous human prostate tissues.Antimicrobial effects of copper(II) bis(thiosemicarbazonato) complexes provide new insight into their biochemical mode of action.Copper Signaling in the Brain and Beyond.Metal Ions Effectively Ablate the Action of Botulinum Neurotoxin A.Selectivity of a thiosemicarbazonatocopper(ii) complex towards duplex RNA. Relevant noncovalent interactions both in solid state and solution.Copper(II), cobalt(II) and nickel(II) complexes of juglone: synthesis, structure, DNA interaction and enhanced cytotoxicity.
P2860
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P2860
Increasing intracellular bioavailable copper selectively targets prostate cancer cells.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Increasing intracellular bioavailable copper selectively targets prostate cancer cells.
@en
Increasing intracellular bioavailable copper selectively targets prostate cancer cells.
@nl
type
label
Increasing intracellular bioavailable copper selectively targets prostate cancer cells.
@en
Increasing intracellular bioavailable copper selectively targets prostate cancer cells.
@nl
prefLabel
Increasing intracellular bioavailable copper selectively targets prostate cancer cells.
@en
Increasing intracellular bioavailable copper selectively targets prostate cancer cells.
@nl
P2093
P50
P356
P1433
P1476
Increasing intracellular bioavailable copper selectively targets prostate cancer cells.
@en
P2093
Kamil Wolyniec
Maree Bilandzic
Michael A Cater
Paul Klaver
Paul S Donnelly
P304
P356
10.1021/CB400198P
P577
2013-05-24T00:00:00Z