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INNOSC Theranostics and
            Pharmacological Sciences                                       Genotoxicity of (4-fluorophenyl) thiazolidin-4-one



               derivatives. Il Farmaco, 57: 747–751.              https://doi.org/10.4103/0250-474X.41448
               https://doi.org/10.1016/S0014-827X(02)01268-5   29.  Kosurkar UB, Mamilla J, Dadmal TL, et al., 2023, Synthesis
                                                                  of novel Thiazolidine-4-One derivatives, their cytotoxicity,
            17.  Rao A, Balzarini J, Carbone A, et al., 2004, Synthesis of new
               2,3-diaryl-1,3-thiazolidin-4-ones as  anti-HIV agents.  Il   antifungal properties, molecular docking and molecular
               Farmaco, 59: 33–39.                                dynamics. Rus J Bioorg Chem, 49, 314–323.
                                                                  https://doi.org/10.1134/S1068162023020127
               https://doi.org/10.1016/j.farmac.2003.09.001
                                                               30.  Gandhi B, Juliya J, Dileep V, et al., 2021, Antioxidant and
            18.  Balzarini J, Orzeszko B, Maurin JK, et al., 2007, Synthesis and
               anti-HIV studies of 2-adamantyl-substituted thiazolidin-4-  biological activities of novel structured monoacylglycerol
               ones. Eur J Med Chem, 42: 993–1003.                derivatives with phenolic acids.  Eur J Lipid Sci Technol,
                                                                  123: 2100055.
               https://doi.org/10.1016/j.ejmech.2007.01.003
                                                                  https://doi.org/10.1002/ejlt.202100055
            19.  Rao A, Chimirri A, Ferro S, et al., 2004, Microwave-induced   31.  Deshpande SS, Veeragoni D, Rachamalla HK, et al., 2022,
               synthesis of benzimidazole and thiazolidinone derivatives as   Anticancer properties of ZnO-Curcumin nanocomposite
               HIV-1 RT inhibitors. Arkivoc, 5: 147–155.
                                                                  against melanoma cancer and its genotoxicity profiling.
               https://doi.org/10.3998/ark.5550190.0005.514       J Drug Deliv Sci Tech, 75: 103703.
            20.  Ravichandran V, Kumar BP, Sankar S, 2009, Predicting anti-     https://doi.org/10.1016/j.jddst.2022.103703
               HIV  activity  of  1,3,4-thiazolidinone  derivaties:  3D-QSAR
               approach. Eur J Med Chem, 44: 1180–1187.        32.  Choudante PC, Nethi SK, Díaz-García D, et al., 2022, Tin-
                                                                  loaded mesoporous silica nanoparticles:  Antineoplastic
               https://doi.org/10.1016/j.ejmech.2008.05.036       properties and genotoxicity assessment.  Biomater Adv,
            21.  Mosula L, Zimenkovsky B, Havrylyuk D,  et al., 2009,   137: 212819.
               Synthesis and antitumor activity of novel 2-thioxo-4-     https://doi.org/10.1016/j.bioadv.2022.212819
               thiazolidinones with benzothiazole moieties.  Farmacia,   33.  Javvaji  K,  Mamilla  J,  Kongari  L,  et  al.,  2023,  In vitro
               57: 321–330.
                                                                  cytogenetic toxicity and cell cycle arrest profiling of
            22.  Dua R, Shrivastava S, Sonwane SK,  et al., 2011,   fluorinated trifluoromethyl 4-Thiazolidinone on CHO-
               Pharmacological significance of synthetic heterocycles   K1 cells. Arch Clin Toxicol, 5: 1–8.
               scaffold: A review. Adv Biol Res, 5: 20–144.
                                                                  https://doi.org/10.46439/toxicology.5.018
            23.  Zahradnik M, 1983, The Production and Application of
               Fluorescent Brightening Agents. Translated by Wilkinson   34.  Bhat M, Poojary B, Kalal BS,  et al., 2018, Synthesis and
               Procharzka ZF. Chichester: Wiley-Interscience, p147.  evaluation of thiazolidinone-pyrazole conjugates as
                                                                  anticancer and antimicrobial agents.  Future Med Chem,
            24.  Naganna MG, Rohini YR, 2014, Synthesis antimicrobial   10: 1017–1036.
               and antioxidant evaluation of 3-(2-(4-fluorobenzylthio)      https://doi.org/10.4155/fmc-2017-0191
               pyrimidin-4-yl-amino)-2-(3-substituted  phenyl)
               thiazolidin-4-ones. World J Pharm Pharm Sci, 3: 1094–1109.  35.  Djukic M, Fesatidou M, Xenikakis I,  et al., 2018,  In vitro
                                                                  antioxidant activity of thiazolidinone derivatives of
            25.  Liu HL, Li Z, Anthonsen T, 2000, Synthesis and fungicidal   1,3-thiazole and 1,3,4-thiadiazole.  Chem Biol Interact,
               activity of 2-imino-3-(4-arylthiazol-2-yl)-thiazolidin-4-ones
               and their 5-arylidene derivatives. Molecules, 5: 1055–1061.   286: 119–131.
                                                                  https://doi.org/10.1016/j.cbi.2018.03.013
               https://doi.org/10.3390/50901055
                                                               36.  Dillehay LE, Denstman SC, Williams JR, 1987, Cell cycle
            26.  Radin NS, 2008, Drug design: Hiding in full view. Drug Dev   dependence of sister chromatid exchange induction by DNA
               Res, 69: 15–25.
                                                                  topoisomerase II inhibitors in Chinese hamster V79 cells.
               https://doi.org/10.1002/ddr.20223                  Can Res, 47: 206–209.
            27.  Thomas AB, Nanda RK, Kothapalli LP, et al., 2013, Synthesis,   37.  Çelik A, Eke D, 2011, The assessment of cytotoxicity and
               biological  activity,  molecular  modelling  studies  and   genotoxicity of tetracycline antibiotic in human blood
               3D-QSAR Investigations of N-[2-(aryl/substituted aryl)-4-  lymphocytes using CBMN and SCE analysis, in vitro. Int J
               oxo-1, 3-thiazolidin-3-yl] pyridine-4-carboxamides.  Open   Hum Gen, 11: 23–29.
               Conf Proc J, 4: 99–112.
                                                                  https://doi.org/10.1080/09723757.2011.11886119
               https://doi.org/10.2174/2210289201304010099
                                                               38.  Hagmar L, Bonassi S, Strömberg U, et al., 1998, Chromosomal
            28.  Taranalli AD, Bhat AR, Srinivas S,  et al., 2008,   aberrations in lymphocytes predict human cancer: A report
               Antiinflammatory,analgesic and antipyretic activity of   from the European Study Group on Cytogenetic Biomarkers
               certain thiazolidinones. Indian J Pharm Sci, 70: 159.   and Health (ESCH). Can Res, 58: 4117–4121.


            Volume 6 Issue 2 (2023)                         9                         https://doi.org/10.36922/itps.0618
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