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Protonated water-soluble N-heterocyclic carbene ruthenium(II) complexes: Synthesis, cytotoxic and DNA binding properties and molecular docking study

https://doi.org/10.1016/j.jorganchem.2018.06.003
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The 110 checked references that resolve
resolves10.1002/anie.201203704
A Continuum of Progress: Applications of N‐Hetereocyclic Carbene Catalysis in Total Synthesis
resolves10.1039/C1SC00621E
Cooperative Lewis acid/N-heterocyclic carbene catalysis
resolves10.1039/c2cs35102a
N-heterocyclic carbene transition metal complexes for catalysis in aqueous media
resolves10.1039/C2DT32617E
N-Heterocyclic carbene metal complexes in medicinal chemistry
resolves10.1021/cr8005153
Coinage Metal−<i>N</i>-Heterocyclic Carbene Complexes
resolves10.1039/C2CS35314H
Metal N-heterocyclic carbene complexes as potential antitumor metallodrugs
resolves10.1007/978-3-642-59914-9_3
Elementspeziesanalytik: Ein Überblick
resolves10.1021/om400819p
Novel Ruthenium(II) and Gold(I) NHC Complexes: Synthesis, Characterization, and Evaluation of Their Anticancer Properties
resolves10.1039/C2DT32319B
Evaluation of arene ruthenium( <scp>ii</scp> ) N-heterocyclic carbene complexes as organometallics interacting with thiol and selenol containing biomolecules
resolves10.1039/B712656P
Antitumour metal compounds: more than theme and variations
resolves10.1039/C7CS00332C
Structure–activity relationships for ruthenium and osmium anticancer agents – towards clinical development
resolves10.1021/jm100020w
Organometallic Anticancer Compounds
resolves10.1039/c3dt33064h
Cationic arene ruthenium(ii) complexes with chelating P-functionalized alkyl phenyl sulfide and sulfoxide ligands as potent anticancer agents
resolves10.1039/C1MT00123J
Advances in metal–carbene complexes as potent anti-cancer agents
resolves10.1016/S0010-8545(99)00039-9
Structural and solution chemistry of gold(I) and silver(I) complexes of bidentate pyridyl phosphines: selective antitumour agents
resolves10.1016/j.jinorgbio.2016.09.004
Ru(II) complexes bearing guanidinium ligands as potent anticancer agents
resolves10.1016/j.jinorgbio.2010.10.016
In vitro antitumour activity of water soluble Cu(I), Ag(I) and Au(I) complexes supported by hydrophilic alkyl phosphine ligands
resolves10.1016/j.jinorgbio.2007.09.003
In vitro antitumour and hepatotoxicity profiles of Au(I) and Ag(I) bidentate pyridyl phosphine complexes and relationships to cellular uptake
resolves10.1155/MBD.1998.217
Antitumor Activity of Gold(I), Silver(I) and Copper(I) ComplexesContaining Chiral Tertiary Phosphines
resolves10.1039/a702757e
Synthesis of gold(I), silver(I) and copper(I) complexes containing substituted (2-aminophenyl)phosphines. Molecular structures of [AuI(2-H2NC6H4PPh2)], [AuI{(±)-2-H2NC6H4PMePh}] and (±)-[Cu(2-H2NC6H4PPh2)2];PF6
resolves10.1002/anie.200703883
Heterocyclic Carbenes: Synthesis and Coordination Chemistry
resolves10.1002/anie.199523711
Metal Complexes of N‐Heterocyclic Carbenes—A New Structural Principle for Catalysts in Homogeneous Catalysis
resolves10.1039/b008038l
A Pd complex of a tridentate pincer CNC bis-carbene ligand as a robust homogenous Heck catalyst
resolves10.1039/b902238b
Beyond catalysis: N-heterocyclic carbene complexes as components for medicinal, luminescent, and functional materials applications
resolves10.1016/j.jorganchem.2010.10.054
Synthesis and anticancer properties of gold(I) and silver(I) N-heterocyclic carbene complexes
resolves10.1021/jm0708679
Synthesis, Stability, and Antimicrobial Studies of Electronically Tuned Silver Acetate <i>N</i>-Heterocyclic Carbenes
resolves10.1002/ejic.200900889
Synthesis, Cytotoxicity and Antibacterial Studies of <i>p</i>‐Methoxybenzyl‐Substituted and Benzyl‐Substituted N‐Heterocyclic Carbene–Silver Complexes
resolves10.1002/zaac.201000395
Synthesis, Cytotoxicity and Antibacterial Studies of Novel Symmetrically and Non‐Symmetrically <i>p</i>‐Nitrobenzyl‐Substituted N‐Heterocyclic Carbene–Silver(I) Acetate Complexes
resolves10.1039/C0MT00034E
Novel benzyl-substituted N-heterocyclic carbene–silver acetate complexes: synthesis, cytotoxicity and antibacterial studies
resolves10.1002/aoc.1702
Synthesis, cytotoxicity and antibacterial studies of symmetrically and non‐symmetrically benzyl‐ or <i>p</i>‐cyanobenzyl‐substituted <i>N</i>‐Heterocyclic carbene–silver complexes
resolves10.1002/hlca.201000310
Synthesis, Cytotoxicity and Antibacterial Studies of Novel Symmetrically and Nonsymmetrically 4‐(Methoxycarbonyl)benzyl‐Substituted <i>N</i>‐Heterocyclic Carbene–Silver Acetate Complexes
resolves10.1016/j.jorganchem.2012.07.006
Novel symmetrically p-benzyl-substituted 4,5-diaryl-imidazole N-heterocyclic carbene-silver(I) acetate complexes – Synthesis and biological evaluation
resolves10.1002/anie.200601663
Palladium Complexes of N‐Heterocyclic Carbenes as Catalysts for Cross‐Coupling Reactions—A Synthetic Chemist's Perspective
resolves10.1039/B316804B
Dinuclear gold( <scp>i</scp> ) complexes of bridging bidentate carbene ligands: synthesis, structure and spectroscopic characterisation
resolves10.1039/B713917A
A cytotoxic bis(carbene)gold( <scp>i</scp> ) complex of ferrocenyl complexes: synthesis and structural characterisation
resolves10.1039/C0DT01089H
[(C <sub>3</sub> H <sub>4</sub> N <sub>2</sub> ) <sub>2</sub> Au]Cl—a bis protic gold( <scp>i</scp> )-NHC
resolves10.1021/om060733d
Synthesis and Characterization of Gold(I) <i>N</i>-Heterocyclic Carbene Complexes Bearing Biologically Compatible Moieties
resolves10.1002/chem.201100321
Cytotoxicity of Gold(I) N‐Heterocyclic Carbene Complexes Assessed by Using Human Tumor Cell Lines
resolves10.1039/c0cc00018c
A N-heterocyclic carbene gold hydroxide complex: a golden synthon
resolves10.1002/aoc.4016
Sulfonated <i>N</i> ‐heterocyclic carbine‐silver (I) complexes: Synthesis, characterisation and biological evaluation
resolves10.1021/jm100801e
Benzimidazol-2-ylidene Gold(I) Complexes Are Thioredoxin Reductase Inhibitors with Multiple Antitumor Properties
resolves10.1021/jm800101w
Gold(I)-Mediated Inhibition of Protein Tyrosine Phosphatases: A Detailed in Vitro and Cellular Study
resolves10.1039/c001216e
Cyclometalated gold(iii) complexes with N-heterocyclic carbene ligands as topoisomerase I poisons
resolves10.1002/chem.200600117
Anticancer Cyclometalated [Au<sup>III</sup><sub><i>m</i></sub>(C<sup>∧</sup>N<sup>∧</sup>C)<sub><i>m</i></sub>L]<sup><i>n</i>+</sup> Compounds: Synthesis and Cytotoxic Properties
resolves10.1039/c1mt00062d
Gold compounds as therapeutic agents for human diseases
resolves10.1039/c1cc10860c
Therapeutic applications of gold complexes: lipophilic gold(iii) cations and gold(i) complexes for anti-cancer treatment
resolves10.1016/j.ccr.2009.02.019
On the medicinal chemistry of gold complexes as anticancer drugs
resolves10.1021/jm00281a001
Oral gold. Antiarthritic properties of alkylphosphinegold coordination complexes
resolves10.1016/j.jorganchem.2005.07.013
Synthesis and structural characterisation of linear Au(I) N-heterocyclic carbene complexes: New analogues of the Au(I) phosphine drug Auranofin
resolves10.1016/j.ccr.2007.04.006
Targeting the mitochondrial cell death pathway with gold compounds
resolves10.1039/C0MD00181C
Thioredoxin reductase, an emerging target for anticancer metallodrugs. Enzyme inhibition by cytotoxic gold(iii) compounds studied with combined mass spectrometry and biochemical assays
resolves10.1002/anie.200502756
Undressing of Phosphine Gold( <scp>I</scp> ) Complexes as Irreversible Inhibitors of Human Disulfide Reductases
resolves10.1039/b602560a
Cationic, linear Au(i) N-heterocyclic carbene complexes: synthesis, structure and anti-mitochondrial activity
resolves10.1002/anie.200601526
Luminescence Studies of the Intracellular Distribution of a Dinuclear Gold(I) N‐Heterocyclic Carbene Complex
resolves10.1016/j.jinorgbio.2004.05.011
Mitochondrial permeability transition induced by dinuclear gold(I)–carbene complexes: potential new antimitochondrial antitumour agents
resolves10.1021/jm201220n
Comparative in Vitro Evaluation of N-Heterocyclic Carbene Gold(I) Complexes of the Benzimidazolylidene Type
resolves10.1002/cmdc.201200055
Anticancer Activity of Silver–<i>N</i>‐Heterocyclic Carbene Complexes: Caspase‐Independent Induction of Apoptosis via Mitochondrial Apoptosis‐Inducing Factor (AIF)
resolves10.1039/b906140a
Synthesis, structural characterisation and anti-proliferative activity of NHC gold amino acid and peptide conjugates
resolves10.1039/c2sc01127a
A spontaneous gold(i)-azide alkyne cycloaddition reaction yields gold-peptide bioconjugates which overcome cisplatin resistance in a p53-mutant cancer cell line
resolves10.1021/jm300428v
Gold(I) Carbene Complexes Causing Thioredoxin <b>1</b> and Thioredoxin <b>2</b> Oxidation as Potential Anticancer Agents
resolves10.1021/jm101096x
Preparation and Characterization of Amino-Linked Heterocyclic Carbene Palladium, Gold, and Silver Complexes and Their Use as Anticancer Agents That Act by Triggering Apoptotic Cell Death
resolves10.2174/187152009787313837
Copper Complexes as Anticancer Agents
resolves10.1016/j.jinorgbio.2006.12.008
Synthesis and mass spectroscopy kinetics of a novel ternary copper(II) complex with cytotoxic activity against cancer cells
resolves10.1021/ic980044x
Preparation of the New Bis(phenanthroline) Ligand “Clip-Phen” and Evaluation of the Nuclease Activity of the Corresponding Copper Complex
resolves10.1021/cr00022a011
Chemical nucleases
resolves10.1021/jm701146c
In Vitro Antitumor Activity of the Water Soluble Copper(I) Complexes Bearing the Tris(hydroxymethyl)phosphine Ligand
resolves10.1039/b719904j
Large-bite bis(phosphite) ligand containing mesocyclic thioether moieties: synthesis, reactivity, group 11 (CuI, AuI) metal complexes and anticancer activity studies on a human cervical cancer (HeLa) cell line
resolves10.1002/chem.200600961
(NHC)Copper(<scp>I</scp>)‐Catalyzed [3+2] Cycloaddition of Azides and Mono‐ or Disubstituted Alkynes
resolves10.1021/bi00377a038
Copper-dependent cleavage of DNA by bleomycin
resolves10.1002/chem.200801992
Toxicity of Copper(I)–NHC Complexes Against Human Tumor Cells: Induction of Cell Cycle Arrest, Apoptosis, and DNA Cleavage
resolves10.1002/cbic.200400243
Cytostatic Activity of 1,10‐Phenanthroline Derivatives Generated by the Clip‐Phen Strategy
resolves10.1021/jm901693m
N-Heterocyclic Carbene-Amine Pt(II) Complexes, a New Chemical Space for the Development of Platinum-Based Anticancer Drugs
resolves10.1016/j.jorganchem.2005.08.020
Synthetic and structural studies of NHC–Pt(dvtms) complexes and their application as alkene hydrosilylation catalysts (NHC = N-heterocyclic carbene, dvtms = divinyltetramethylsiloxane)
resolves10.1039/c0sc00593b
Luminescent cyclometalated platinum(ii) complexes containing N-heterocyclic carbene ligands with potent in vitro and in vivo anti-cancer properties accumulate in cytoplasmic structures of cancer cells
resolves10.1039/c1cc11391g
Direct functionalisation of group 10 N-heterocyclic carbene complexes for diversity enhancement
resolves10.1039/B912608B
Metal chelating systems synthesized using the copper(i) catalyzed azide-alkynecycloaddition
resolves10.1016/j.tetlet.2005.01.033
A palladium Chugaev carbene complex as a modular, air-stable catalyst for Suzuki–Miyaura cross-coupling reactions
resolves10.1039/c1cc12228b
A platinum Chugaev carbene complex as a potent anticancer agent
resolves10.1002/ejic.200800366
The Synthesis of Ruthenium and Rhodium Complexes with Functionalized N‐Heterocyclic Carbenes and Their Use in Solid Phase Peptide Synthesis
resolves10.1016/j.jorganchem.2010.12.044
Organometallic peptide NHC complexes of Cp∗Rh(III) and arene Ru(II) moieties from l-thiazolylalanine
resolves10.1517/17425250902882128
The use of<i>in vivo</i>zebrafish assays in drug toxicity screening
resolves10.1089/zeb.2009.0601
Biomedical Properties of a Series of Ruthenium-N-Heterocyclic Carbene Complexes Based on Oxidant Activity <i>In Vitro</i> and Assessment <i>In Vivo</i> of Biosafety in Zebrafish Embryos
resolves10.1016/S0010-8545(02)00312-0
Ruthenium metallopharmaceuticals
resolves10.1595/003214001X4526269
Ruthenium in Medicine: Current Clinical Uses and Future Prospects
resolves10.1155/2015/859730
Anticancer Activities of Mononuclear Ruthenium(II) Coordination Complexes
resolves10.1039/c0dt01816c
Ruthenium anticancer compounds: myths and realities of the emerging metal-based drugs
resolves10.1016/j.jinorgbio.2011.09.030
Approaching tumour therapy beyond platinum drugs
resolves10.1016/j.biomaterials.2012.01.057
Ruthenium-based complex nanocarriers for cancer therapy
resolves10.1021/bc200565v
Cholesterol-Based Nucleolipid-Ruthenium Complex Stabilized by Lipid Aggregates for Antineoplastic Therapy
resolves10.1002/ejic.201300820
Synthesis, Cellular Uptake and Biological Activity Against Pathogenic Microorganisms and Cancer Cells of Rhodium and Iridium N‐Heterocyclic Carbene Complexes Bearing Charged Substituents
resolves10.1021/om500140g
Template-Directed Synthesis of Palladium(II) Sulfonate-NHC Complexes and Catalytic Studies in Aqueous Mizoroki–Heck Reactions
resolves10.1007/BF02376078
Triple ion-type imidazolium salts: A new class of single-ion conductive matrix
resolves10.1021/om500753v
Water-Soluble Mono- and Dimethyl N-Heterocyclic Carbene Platinum(II) Complexes: Synthesis and Reactivity
resolves10.1016/S0022-328X(01)01029-4
Synthesis of a water-soluble carbene complex and its use as catalyst for the synthesis of 2,3-dimethylfuran
resolves10.1021/cr800403r
Hydrophilic Ligands and Their Application in Aqueous-Phase Metal-Catalyzed Reactions
resolves10.1351/pac200072071365
Diels_Alder reactions in water
resolves10.1002/anie.200502882
Hydrophobically Directed Organic Synthesis
resolves10.1016/j.jorganchem.2016.01.018
Novel multicharged silver(I)–NHC complexes derived from zwitterionic 1,3-symmetrically and 1,3-unsymmetrically substituted imidazoles and benzimidazoles: Synthesis and cytotoxic properties
resolves10.1016/j.jinorgbio.2013.09.011
Synthesis and in vitro antitumor activity of water soluble sulfonate- and ester-functionalized silver(I) N-heterocyclic carbene complexes
resolves10.1021/om9010966
Syntheses, Structures, and Catalytic Activities of Hemilabile Thioether-Functionalized NHC Complexes
resolves10.1016/j.ica.2009.02.035
Synthesis, structural characterization and catalytic activity of a palladium(II) complex bearing a new ditopic thiophene-N-heterocyclic carbene ligand
resolves10.1016/j.tetasy.2010.06.041
Axially chiral C2-symmetric N-heterocyclic carbene (NHC) palladium complexes-catalyzed asymmetric arylation of aldehydes with arylboronic acids
resolves10.1016/j.jorganchem.2005.09.015
A new paradigm in N-heterocyclic carbenoid ligands
resolves10.1002/hlca.201100107
Novel Benzyl‐ or 4‐Cyanobenzyl‐Substituted N‐Heterocyclic (Bromo)(carbene)silver(I) and (Carbene)(chloro)gold(I) Complexes: Synthesis and Preliminary Cytotoxicity Studies
resolves10.1039/c1cc15908a
Silver metallation of hen egg white lysozyme: X-ray crystal structure and NMR studies
resolves10.1016/j.ica.2012.10.029
Synthesis and biological evaluation of N-heterocyclic carbene–silver(I) acetate complexes derived from 4,5-ditolyl-imidazole
resolves10.1016/j.jorganchem.2015.04.012
Novel ruthenium(II)–N-heterocyclic carbene complexes; synthesis, characterization and catalytic application
resolves10.1080/00958972.2014.911291
Synthesis, characterization, and transfer hydrogenation of Ru(II)-<i>N</i>-heterocyclic carbene complexes
resolves10.1016/j.jorganchem.2012.01.001
Water-soluble carbene complexes as catalysts for the hydrogenation of acetophenone under hydrogen pressure
resolves10.3390/ijms18091856
PSFM-DBT: Identifying DNA-Binding Proteins by Combing Position Specific Frequency Matrix and Distance-Bigram Transformation
The 13 references without a DOI — listed, not checked
no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib3
no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib14b
no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib14c
no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib19d
no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib19e
no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib20a
no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib20d
no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib21a
no DOI — not checkedP. Mailliet, A. Marinetti and M. Skander, WO/2009/118475, 2009.
no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib24c
no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib25
no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib36
no DOI — not checked10.1016/j.jorganchem.2018.06.003_bib37
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