Organometallic ruthenium and iridium transfer-hydrogenation catalysts using coenzyme NADH as a cofactor.
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The potent oxidant anticancer activity of organoiridium catalysts.Using non-enzymatic chemistry to influence microbial metabolismTransfer hydrogenation catalysis in cells as a new approach to anticancer drug design.Antimicrobial metallopeptides with broad nuclease and ribonuclease activity.Organometallic Iridium(III) anticancer complexes with new mechanisms of action: NCI-60 screening, mitochondrial targeting, and apoptosis.Organoiridium complexes: anticancer agents and catalystsMetal complex catalysis in living biological systems.The coordination chemistry of organo-hydride donors: new prospects for efficient multi-electron reduction.Innocent But Deadly: Nontoxic Organoiridium Catalysts Promote Selective Cancer Cell Death.The contrasting catalytic efficiency and cancer cell antiproliferative activity of stereoselective organoruthenium transfer hydrogenation catalysts.Imino Transfer Hydrogenation Reductions.Synthesis, characterisation and biological activities of [(p-cym)RuX(pz4lut)]n+ and [{(p-cym)RuX}2(μ-pz4lut)]n+ (X = Cl, H2O and pz4lut = α,α,α',α'-tetra(pyrazol-1-yl)-2,6-lutidine).Reduction of quinones by NADH catalyzed by organoiridium complexes.Contrasting Anticancer Activity of Half-Sandwich Iridium(III) Complexes Bearing Functionally Diverse 2-Phenylpyridine Ligands.Synthetic cascades are enabled by combining biocatalysts with artificial metalloenzymes.Hydrogen generation from methanol at near-room temperature.Novel half-sandwich iridium(iii) imino-pyridyl complexes showing remarkable in vitro anticancer activity.Iridium(iii) complexes with five-membered heterocyclic ligands for combined photodynamic therapy and photoactivated chemotherapy.Half-sandwich iridium N-heterocyclic carbene anticancer complexes.Half-sandwich ruthenium(ii) complexes containing N^N-chelated imino-pyridyl ligands that are selectively toxic to cancer cells.Designing organometallic compounds for catalysis and therapy.Catalytic Metallodrugs: Substrate-Selective Metal Catalysts as Therapeutics.Renewable Molecular Flasks with NADH Models: Combination of Light-Driven Proton Reduction and Biomimetic Hydrogenation of Benzoxazinones.Immobilization of an artificial imine reductase within silica nanoparticles improves its performance.The contrasting chemical reactivity of potent isoelectronic iminopyridine and azopyridine osmium(ii) arene anticancer complexes
P2860
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P2860
Organometallic ruthenium and iridium transfer-hydrogenation catalysts using coenzyme NADH as a cofactor.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
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2012年学术文章
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2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
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2012年學術文章
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name
Organometallic ruthenium and i ...... g coenzyme NADH as a cofactor.
@en
Organometallic ruthenium and i ...... g coenzyme NADH as a cofactor.
@nl
type
label
Organometallic ruthenium and i ...... g coenzyme NADH as a cofactor.
@en
Organometallic ruthenium and i ...... g coenzyme NADH as a cofactor.
@nl
prefLabel
Organometallic ruthenium and i ...... g coenzyme NADH as a cofactor.
@en
Organometallic ruthenium and i ...... g coenzyme NADH as a cofactor.
@nl
P2093
P2860
P356
P1476
Organometallic ruthenium and i ...... g coenzyme NADH as a cofactor.
@en
P2093
Bushra Qamar
Peter J Sadler
Soledad Betanzos-Lara
P2860
P304
P356
10.1002/ANIE.201108175
P407
P577
2012-03-13T00:00:00Z