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.
The 52 checked references that resolve
resolves10.1039/c3sc22205eGlucose conjugation for the specific targeting and treatment of cancer
resolves10.1042/bj1310211Structural requirements for binding to the sugar-transport system of the human erythrocyte
resolves10.3389/fchem.2018.00386Protected and De-protected Platinum(IV) Glycoconjugates With GLUT1 and OCT2-Mediated Selective Cancer Targeting: Demonstrated Enhanced Transporter-Mediated Cytotoxic Properties in vitro and in vivo
resolves10.3390/nu6104165The Role of Sodium-Dependent Glucose Transporter 1 and Glucose Transporter 2 in the Absorption of Cyanidin-3-O-β-Glucoside in Caco-2 Cells
resolves10.2147/DDDT.S497638-Hydroxyquinolines: a review of their metal chelating properties and medicinal applications
resolves10.1039/C4MD00284A8-Hydroxyquinoline: a privileged structure with a broad-ranging pharmacological potential
resolves10.1016/j.bioorg.2018.11.047Synthesis of 8-hydroxyquinoline glycoconjugates and preliminary assay of their β1,4-GalT inhibitory and anti-cancer properties
resolves10.3390/molecules242241818-Hydroxyquinoline Glycoconjugates: Modifications in the Linker Structure and Their Effect on the Cytotoxicity of the Obtained Compounds
resolves10.1021/acs.biochem.7b00268The Sulfur-Linked Analogue of O-GlcNAc (S-GlcNAc) Is an Enzymatically Stable and Reasonable Structural Surrogate for O-GlcNAc at the Peptide and Protein Levels
resolves10.1021/jo500883vDesign and Synthesis of Hydrolytically Stable Multivalent Ligands Bearing Thiodigalactoside Analogues for Peanut Lectin and Human Galectin-3 Binding
resolves10.1007/s00253-005-0156-xThiosugars: new perspectives regarding availability and potential biochemical and medicinal applications
resolves10.7150/ijms.4.131Thioglycosides as inhibitors of hSGLT1 and hSGLT2: Potential therapeutic agents for the control of hyperglycemia in diabetes
resolves10.1080/15257770.2015.1109098Synthesis and Antimicrobial Screening of Novel Thioglycosides and Acyclonucleoside Analogs Carrying 1,2,3-Triazole and 1,3,4-Oxadiazole Moieties
resolves10.1021/jm070669hSynthesis of Natural Product-Inspired Inhibitors of <i>Mycobacterium tuberculosis</i> Mycothiol-Associated Enzymes: The First Inhibitors of GlcNAc-Ins Deacetylase
resolves10.1016/j.bbapap.2014.01.006Antiglioma activity of GoPI-sugar, a novel gold(I)–phosphole inhibitor: Chemical synthesis, mechanistic studies, and effectiveness in vivo
resolves10.1039/b706423cAsymmetric sulfur atom coordination in a copper(ii) dipicolylamine (DPA) complex with a thioglycoside ligand
resolves10.1246/bcsj.56.3258Copper(II)-Sulfur Interactions in Pyridine- and Imidazole-containing Disulfide Complexes. Syntheses, Spectra, and Solution Equilibria
resolves10.1021/jo010705zSynthesis of Cyclodextrin-Based Carbohydrate Clusters by Photoaddition Reactions
resolves10.1021/jo035300oGlycosylthiomethyl Chloride: A New Species for <i>S</i>-Neoglycoconjugate Synthesis. Synthesis of 1-<i>N</i>-Glycosylthiomethyl-1,2,3-triazoles
resolves10.1016/j.bmc.2016.03.065Design, synthesis and biological evaluation of LBM-A5 derivatives as potent P-glycoprotein-mediated multidrug resistance inhibitors
resolves10.1016/j.ccr.2011.06.028The copper(I)-catalyzed alkyne-azide cycloaddition (CuAAC) “click” reaction and its applications. An overview
resolves10.3390/cancers12010154Targeting Glucose Transporters for Breast Cancer Therapy: The Effect of Natural and Synthetic Compounds
resolves10.1016/j.bcp.2003.10.031Organic copper complexes as a new class of proteasome inhibitors and apoptosis inducers in human cancer cells
The 4 references without a DOI — listed, not checked
no DOI — not checkedEfficient Synthesis of Glycosylated Asparaginic Acid Building Blocks via Click Chemistry
no DOI — not checkedA facile and efficient synthesis of S-glycosylated derivatives of 5-nitropyridine
no DOI — not checked(2020, August 30). β-Galactosidase from Aspergillus oryzae (G5160)-Enzyme Assay. Available online: https://www.sigmaaldrich.com/content/dam/sigma-aldrich/docs/Sigma/Enzyme_Assay/g5160enz.pdf.
no DOI — not checkedNovel 8-hydroxylquinoline analogs induce copper-dependent proteasome inhibition and cell death in human breast cancer cells
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