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Triapine Analogues and Their Copper(II) Complexes: Synthesi..:

Iuliana Besleaga (11153522) ; Iryna Stepanenko (9111146) ; Tatsiana V. Petrasheuskaya (11153525)...
https://figshare.com/articles/journal_contribution/Triapine_Analogues_and_Their_Copper_II_Complexes_Synthesis_Characterization_Solution_Speciation_Redox_Activity_Cytotoxicity_and_mR2_RNR_Inhibition/15016136. , 2021

Link: https://doi.org/10.1021/acs.inorgchem.1c01275.s001

RT Journal
T1 <Title>Triapine Analogues and Their Copper(II) Complexes: Synthesis, Characterization, Solution Speciation, Redox Activity, Cytotoxicity, and mR2 RNR Inhibition</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_15016136&Exemplar=1&LAN=DE
				
A1 Iuliana Besleaga (11153522)
A1 Iryna Stepanenko (9111146)
A1 Tatsiana V. Petrasheuskaya (11153525)
A1 Denisa Darvasiova (6094814)
A1 Martin Breza (1584697)
A1 Marta Hammerstad (436201)
A1 Małgorzata A. Marć (11153528)
A1 Alexander Prado-Roller (9869035)
A1 Gabriella Spengler (371096)
A1 Ana Popović-Bijelić (1713028)
A1 Eva A. Enyedy (5628341)
A1 Peter Rapta (1584691)
A1 Anatoly D. Shutalev (1997638)
A1 Vladimir B. Arion (1275156)
YR 2021
K1 Biophysics
K1 Biochemistry
K1 Microbiology
K1 Cell Biology
K1 Cancer
K1 Environmental Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 anodic region
K1 monocationic complexes
K1 Redox Activity
K1 Complexes 1
K1 micromolar concentration range
K1 electrochemical oxidation
K1 pH range
K1 solution speciation studies
K1 MRC
K1 mR 2 ribonucleotide reductase
K1 antiproliferative activity
K1 chemical oxidations
K1 TSC
K1 fibroblast cells
K1 concentration values
K1 one-electron reduction
K1 dimethyl sulfoxide
K1 anoxic methanol
K1 four-electron oxidation products
K1 resonance spectroelectrochemistry
K1 HL 1
K1 HL 2
K1 Z isomers
K1 cancer cells
K1 nitrogen atom
K1 terminal nitrogen atom
K1 Cu
K1 redox-active phenolic moiety
K1 Colo 205
K1 Colo 320 cancer cell lines
K1 triapine analogues
K1 ligand-centered oxidation
K1 mR 2 RNR Inhibition
K1 Schiff base imine bond
K1 pH 7.4. Electrochemical
K1 spectroelectrochemical studies
K1 Solution Speciation
K1 metal-free ligands
JF https://figshare.com/articles/journal_contribution/Triapine_Analogues_and_Their_Copper_II_Complexes_Synthesis_Characterization_Solution_Speciation_Redox_Activity_Cytotoxicity_and_mR2_RNR_Inhibition/15016136
LK http://dx.doi.org/https://doi.org/10.1021/acs.inorgchem.1c01275.s001
DO https://doi.org/10.1021/acs.inorgchem.1c01275.s001
SF ELIB - SuUB Bremen

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