Interaction of Triapine and related thiosemicarbazones with iron(III)/(II) and gallium(III): a comparative solution equilibrium study. - Wikidata - wikimedia - TriplyDB

Interaction of Triapine and related thiosemicarbazones with iron(III)/(II) and gallium(III): a comparative solution equilibrium study.

Interaction of Triapine and related thiosemicarbazones with iron(III)/(II) and gallium(III): a comparative solution equilibrium study.

http://www.wikidata.org/entity/Q36025551

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Ribonucleotide reductase metallocofactor: assembly, maintenance and inhibition.Design and synthesis of novel N()-substituted thiosemicarbazones bearing a pyrrole unit as potential anticancer agents.Iron homeostasis and tumorigenesis: molecular mechanisms and therapeutic opportunities Strong effect of copper(II) coordination on antiproliferative activity of thiosemicarbazone-piperazine and thiosemicarbazone-morpholine hybrids.Impact of terminal dimethylation on the resistance profile of α-N-heterocyclic thiosemicarbazones Mechanistic studies of semicarbazone triapine targeting human ribonucleotide reductase in vitro and in mammalian cells: tyrosyl radical quenching not involving reactive oxygen species.Iron-targeting antitumor activity of gallium compounds and novel insights into triapine(®)-metal complexes.Ribonucleotide reductase inhibition by metal complexes of Triapine (3-aminopyridine-2-carboxaldehyde thiosemicarbazone): a combined experimental and theoretical study.Synthesis, characterisation and antitubercular activities of a series of pyruvate-containing aroylhydrazones and their Cu-complexes.Gallium(III) complexes with 2-acetylpyridine-derived thiosemicarbazones: antimicrobial and cytotoxic effects and investigation on the interactions with tubulin.Piperazinyl fragment improves anticancer activity of Triapine.Effects of Terminal Substitution and Iron Coordination on Antiproliferative Activity of l -Proline-salicylaldehyde-Thiosemicarbazone Hybrids Complex-Formation Ability of Salicylaldehyde Thiosemicarbazone towards ZnII, CuII, FeII, FeIIIand GaIIIIons

P2860

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P2860

Interaction of Triapine and related thiosemicarbazones with iron(III)/(II) and gallium(III): a comparative solution equilibrium study.

http://www.wikidata.org/entity/Q36025551

description

2011 nî lūn-bûn

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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Interaction of Triapine and re ...... ve solution equilibrium study.

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Interaction of Triapine and re ...... ve solution equilibrium study.

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Interaction of Triapine and re ...... ve solution equilibrium study.

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Interaction of Triapine and re ...... ve solution equilibrium study.

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Interaction of Triapine and re ...... ive solution equilibrium study

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Michael F Primik

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Tamás Kiss

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Vladimir B Arion

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P2860

Miniquad-A general computer programme for the computation of formation constants from potentiometric data.

An electrochemical study of antineoplastic gallium, iron and ruthenium complexes with redox noninnocent alpha-N-heterocyclic chalcogensemicarbazones.

A class of iron chelators with a wide spectrum of potent antitumor activity that overcomes resistance to chemotherapeutics.

Thiosemicarbazones from the old to new: iron chelators that are more than just ribonucleotide reductase inhibitors.

Fluorescence properties and cellular distribution of the investigational anticancer drug triapine (3-aminopyridine-2-carboxaldehyde thiosemicarbazone) and its zinc(II) complex.

2-Acetylpyridine thiosemicarbazones are potent iron chelators and antiproliferative agents: redox activity, iron complexation and characterization of their antitumor activity.

Gallium(III) complexes of 2-pyridineformamide thiosemicarbazones: cytotoxic activity against malignant glioblastoma.

Gallium(III) and iron(III) complexes of alpha-N-heterocyclic thiosemicarbazones: synthesis, characterization, cytotoxicity, and interaction with ribonucleotide reductase.

Novel Schiff base copper complexes of quinoline-2 carboxaldehyde as proteasome inhibitors in human prostate cancer cells.

A Ferrous-Triapine complex mediates formation of reactive oxygen species that inactivate human ribonucleotide reductase.

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10.1039/C0DT01835J

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22

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40

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Bernhard K. Keppler

Christian R Kowol

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2011-04-27T00:00:00Z

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3372890

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