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For: Mech D, Kurowska A, Trotsko N. The Bioactivity of Thiazolidin-4-Ones: A Short Review of the Most Recent Studies. Int J Mol Sci 2021;22:11533. [PMID: 34768964 DOI: 10.3390/ijms222111533] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Mishchenko M, Shtrygol’ S, Lozynskyi A, Hoidyk M, Khyluk D, Gorbach T, Lesyk R. Evaluation of 5-[(Z)-(4-nitrobenzylidene)]-2-(thiazol-2-ylimino)-4-thiazolidinone (Les-6222) as Potential Anticonvulsant Agent. Sci Pharm 2022;90:56. [DOI: 10.3390/scipharm90030056] [Reference Citation Analysis]
2 Rehulka J, Subtelna I, Kryshchyshyn‐dylevych A, Cherniienko A, Ivanova A, Matveieva M, Polishchuk P, Gurska S, Hajduch M, Zagrijtschuk O, Dzubak P, Lesyk R. Anticancer 5‐arylidene‐2‐(4‐hydroxyphenyl)aminothiazol‐4(5 H )‐ones as tubulin inhibitors. Archiv der Pharmazie. [DOI: 10.1002/ardp.202200419] [Reference Citation Analysis]
3 Bar M, Skóra B, Tabęcka-łonczyńska A, Holota S, Khyluk D, Roman O, Lesyk R, Szychowski KA. New 4-thiazolidinone-based molecules Les-2769 and Les-3266 as possible PPARγ modulators. Bioorganic Chemistry 2022. [DOI: 10.1016/j.bioorg.2022.106075] [Reference Citation Analysis]
4 Yıldırım A, Öztürk S. An Efficient Ni(II) Laurate Promoted Heterocyclization of Symmetrical Thioureas with Maleic Anhydride and Mechanistic Approach toward Higher Substituted Thiazolidine‐4‐one‐5‐acetic Acids. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202201957] [Reference Citation Analysis]