has been cited by the following article(s):
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[1]
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Novel bis-Thiazolidinone -based chalcones with pyridine linker: Eco-friendly synthesis, cholinesterase and beta-amyloid inhibition potency, and molecular docking studies
Bioorganic Chemistry,
2026
DOI:10.1016/j.bioorg.2025.109372
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[2]
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Design, Syntheses and Biological Evaluation of 4-Aminoquinoline-Thiazolidinone Hybrids
Chemistry Africa,
2025
DOI:10.1007/s42250-025-01232-0
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[3]
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Synthesis and insecticidal activity of new 5-((3-(5-methyl-1-phenyl-1H-1,2,3-triazol-4-yl)-1-phenyl-1H-pyrazol-4-yl)methylene)thiazolidin-4-ones
Journal of Molecular Structure,
2025
DOI:10.1016/j.molstruc.2025.142673
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[4]
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Drug Design, In Silico-Profiling of New Pyrrole Derivatives: Promising Anticancer Agents Against Acute Myeloid Leukemia
Al Mustansiriyah Journal of Pharmaceutical Sciences,
2024
DOI:10.32947/ajps.v24i3.1063
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[5]
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Novel antipyrine substituted 4-thiazolidinones: Synthesis, DNA binding and topoisomerase inhibition activities, and in-silico studies
Journal of Molecular Structure,
2024
DOI:10.1016/j.molstruc.2024.139192
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[6]
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Synthesis, single crystal, in-silico and in-vitro assessment of the thiazolidinones
Journal of Molecular Structure,
2022
DOI:10.1016/j.molstruc.2022.132384
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[7]
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Nucleosides 11: synthesis of new derivatives of pyrido[2,3-d]pyrimidines and their nucleosides
Nucleosides, Nucleotides & Nucleic Acids,
2020
DOI:10.1080/15257770.2020.1862869
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