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A Fluorescent Silver(I) Carbene Complex with Anticancer Properties: Synthesis, Characterization, and Biological Studies

https://doi.org/10.1002/cmdc.201800672
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Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.

8 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.

The 30 checked references that resolve
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The Next Generation of Platinum Drugs: Targeted Pt(II) Agents, Nanoparticle Delivery, and Pt(IV) Prodrugs
resolves10.2174/156802611794785226
Transition Metal Based Anticancer Drugs
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Next-Generation Metal Anticancer Complexes: Multitargeting via Redox Modulation
resolves10.1038/nrc2167
The resurgence of platinum-based cancer chemotherapy
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Arsenic trioxide — An old drug rediscovered
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A New Approach to Reduce Toxicities and to Improve Bioavailabilities of Platinum-Containing Anti-Cancer Nanodrugs
resolves10.1038/bjc.2017.392
The combined activation of KCa3.1 and inhibition of Kv11.1/hERG1 currents contribute to overcome Cisplatin resistance in colorectal cancer cells
resolves10.1039/C2DT32617E
N-Heterocyclic carbene metal complexes in medicinal chemistry
resolves10.1021/cr800500u
The Medicinal Applications of Imidazolium Carbene−Metal Complexes
resolves10.1002/chem.201601542
Iridium(I) Compounds as Prospective Anticancer Agents: Solution Chemistry, Antiproliferative Profiles and Protein Interactions for a Series of Iridium(I) N‐Heterocyclic Carbene Complexes
resolves10.1016/j.poly.2014.05.067
{Ru(CO)x}-core complexes with selected azoles: Synthesis, X-ray structure, spectroscopy, DFT analysis and evaluation of cytotoxic activity against human cancer cells
resolves10.1039/c0cc01465f
Reactions of medicinally relevant gold compounds with the C-terminal motif of thioredoxin reductase elucidated by MS analysis
resolves10.1016/j.jinorgbio.2014.01.009
Insights on the mechanism of thioredoxin reductase inhibition by Gold N-heterocyclic carbene compounds using the synthetic linear Selenocysteine containing C-terminal peptide hTrxR(488-499): An ESI-MS investigation
resolves10.3390/molecules200712732
Metal- and Semimetal-Containing Inhibitors of Thioredoxin Reductase as Anticancer Agents
resolves10.1039/c3mt20260g
Fluorescent silver(i) and gold(i)–N-heterocyclic carbene complexes with cytotoxic properties: mechanistic insights
resolves10.1039/C5DT01196E
cis-Pt I <sub>2</sub> (NH <sub>3</sub> ) <sub>2</sub> : a reappraisal
resolves10.1021/jm300428v
Gold(I) Carbene Complexes Causing Thioredoxin <b>1</b> and Thioredoxin <b>2</b> Oxidation as Potential Anticancer Agents
resolves10.1002/cmdc.201402049
Gold(I) <i>N</i>‐Heterocyclic Carbene Complexes with Naphthalimide Ligands as Combined Thioredoxin Reductase Inhibitors and DNA Intercalators
resolves10.1021/acsmedchemlett.7b00162
Auranofin, Et<sub>3</sub>PAuCl, and Et<sub>3</sub>PAuI Are Highly Cytotoxic on Colorectal Cancer Cells: A Chemical and Biological Study
resolves10.1002/chem.201605801
Protein Metalation by Anticancer Metallodrugs: A Joint ESI MS and XRD Investigative Strategy
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Gold(III) complexes with hydroxyquinoline, aminoquinoline and quinoline ligands: Synthesis, cytotoxicity, DNA and protein binding studies
resolves10.1016/j.jinorgbio.2016.09.016
Antiproliferative properties and biomolecular interactions of three Pd(II) and Pt(II) complexes
resolves10.1016/j.talanta.2017.01.074
Mass spectrometry and metallomics: A general protocol to assess stability of metallodrug-protein adducts in bottom-up MS experiments
resolves10.1021/ic402611m
Peculiar Features in the Crystal Structure of the Adduct Formed between<i>cis</i>-PtI<sub>2</sub>(NH<sub>3</sub>)<sub>2</sub>and Hen Egg White Lysozyme
resolves10.1039/C7CC06442J
Protein metalation by metal-based drugs: X-ray crystallography and mass spectrometry studies
resolves10.1021/cr050004s
Ag(I) N-Heterocyclic Carbene Complexes:  Synthesis, Structure, and Application
resolves10.1021/jo971176v
NMR Chemical Shifts of Common Laboratory Solvents as Trace Impurities
resolves10.1107/S0021889898007717
<i>SIR</i>97: a new tool for crystal structure determination and refinement
resolves10.1107/S0108767307043930
A short history of<i>SHELX</i>
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