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References from Design, synthesis, and preliminary in vitro screening of novel tolmetin hydrazones against colon cancer. Local targets link to admitted publications; unresolved targets remain external evidence.
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Synthesis of tolmetin hydrazide-hydrazones and discovery of a potent apoptosis inducer in colon cancer cells
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Studying the efficacy of tolmetin radiosensitizing effect in radiotherapy treatment on human clonal cancer cells
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Design, synthesis, anticancer evaluation, and molecular modelling studies of novel tolmetin derivatives as potential VEGFR-2 inhibitors and apoptosis inducers
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Synthesis and anticancer activity of tolmetin thiosemicarbazides
2015 · External reference
Biological activities of hydrazone derivatives
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Hydrazide-hydrazone/hydrazone as enabling linkers in anti-cancer drug discovery: a comprehensive review
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Design and synthesis of novel (S)-naproxen hydrazide-hydrazones as potent VEGFR-2 inhibitors and their evaluation in vitro/in vivo breast cancer models
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Rational design, synthesis and anti-proliferative evaluation of novel benzosuberone tethered with hydrazide–hydrazones
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Imidazole-based hydrazones as potent anti-colon cancer agents: design, synthesis, biological evaluation and computational studies
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Synthesis of novel diflunisal hydrazide-hydrazones as anti-hepatitis C virus agents and hepatocellular carcinoma inhibitors
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Novel hydrazide-hydrazone derivatives containing flurbiprofen 1,2,4-triazole as anticancer agents: design, synthesis and biological evaluation
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Conformational behaviour and E/Z isomerization of N-acyl and N-aroylhydrazones
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Assessing the cytotoxicity of phenolic and terpene fractions extracted from Iraqi Prunus arabica against AMJ13 and SK-GT-4 human cancer cell lines
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Mitochondrial inner membrane depolarization as a marker of platelet apoptosis
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Investigation of novel nimesulide derivatives against breast cancer
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The detailed comparison of cell death detected by Annexin V-PI counterstain using fluorescence microscope, flow cytometry and automated cell counter in mammalian and microalgae cells
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Design and development of COX-II inhibitors: current scenario and future perspective
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Action at a distance: mutations of peripheral residues transform rapid reversible inhibitors to slow, tight binders of cyclooxygenase-2
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