References

• • Atioğlu, Z., Sevinçli, Z. Ş., Karalı, N., Akkurt, M., & Ersanlı C. C. (2017a). 2-(5-Fluoro-1-methyl-2-oxoindolin-3-ylidene)-N-[4- (methylsulfanyl)phenyl]hydrazine-1-carbothioamide. IUCrData, 2(5), x170671. google scholar
• • Atioğlu, Z., Sevinçli, Z. Ş., Karalı, N., Akkurt, M., & Ersanlı C. C. (2017b). (2Z)-2-(5-Fluoro-1-methyl-2-oxoindolin-3-ylidene)- N-(3-fluorophenyl)hydrazine-1-carbothioamide. IUCrData, 2(6), x170900. google scholar
• • Banerjee, D., Yogeeswari, P., Bhat, P., Thomas, A., Srividya, M., & Sriram, D. (2011). Novel isatinyl thiosemicarbazones derivatives as potential molecule to combat HIV-TB co-infection. European Journal of Medicinal Chemistry, 46(1), 106−121. google scholar
• • Brimacombe K., Fales H. M., Gottesman M. M., Hall, M. D., & Handley, M. (2012). W.O. Patent No. 2012033601 A1. google scholar
• • Dikmen, M., Özturk, N., & Özturk, Y. The antioxidant potency of Punica granatum L. Fruit peel reduces cell proliferation and induces apoptosis on breast cancer. Journal of Medicinal Food, 14(12), 1638−1646. google scholar
• • Feng, L. S., Liu, M. L., Wang, B., Chai, Y., Hao, X. Q., Meng, S., & Guo, H. Y. (2010). Synthesis and in vitro antimycobacterial activity of balofloxacin ethylene isatin derivatives. European Journal of Medicinal Chemistry, 45, 3407−3412. google scholar
• • Foongladda, S., Roengsanthia, D., Arjrattanakool, W., Chuchottaworn, C., Chaiprasert, A., & Franzblau, S. G. (2002). Rapid and simple MTT method for rifampicin and isoniazid susceptibility testing of Mycobacterium tuberculosis. The International Journal of Tuberculosis and Lung Disease, 6(12), 1118−1122. google scholar
• • Güzel, Ö., Karalı, N., & Salman, A. (2008). Synthesis and antituberculosis activity of 5-methyl/ trifluoromethoxy-1H-indole-2,3- dione 3-thiosemicarbazone derivatives. Bioorganic & Medicinal Chemistry, 16(19), 8976−8987. google scholar
• • Hall, M. D., Salam, N. K., Hellawell, J. L., Fales, H. M., Kensler, C. B., Ludwig, J. A. … Gottesman, M. M. (2009). Synthesis, activity, and pharmacophore development for isatin-β-thiosemicarbazones with selective activity toward multidrug-resistant cells. Journal of Medicinal Chemistry, 52(10), 3191−3204. google scholar
• • Hall, M. D., Gottesman, M. M., Hellawell, J. L., Ludwig, J. A., Fales, H. M., Salam, N. K., & Szakács, G. (2010). U.S. Patent Application No. 12/867,206. google scholar
• • Hall, M. D., Brimacombe, K. R., Varonka, M. S., Pluchino, K. M., Monda, J. K., Li, J. … Gottesman, M. M. (2011). Synthesis and structureactivity evaluation of isatin-β-thiosemicarbazones with improved selective activity toward multidrug-resistant cells expressing Pglycoprotein. Journal of Medicinal Chemistry, 54, 5878−5889. google scholar
• • Karalı, N. (2002). Synthesis and primary cytotoxicity evaluation of new 5-nitroindole-2,3-dione derivatives. European Journal of Medicinal Chemistry, 37(11), 909−918. google scholar
• • Karalı, N., Gürsoy, A., Kandemirli, F., Shvets, N., Kaynak, F. B.,Özbey, S. … Dimoglo, A. (2007). Synthesis and structure–antituberculosis activity relationship of 1H-indole-2,3-dione derivatives. Bioorganic & Medicinal Chemistry, 15(17), 5888−5904. google scholar
• • Karalı, N., Akdemir, A., Göktaş, F., Eraslan-Elma, P., Angeli, A., Kızılırmak, M. & Supuran, C. T. (2017). Novel sulfonamide-containing 2-indolinones that selectively inhibit tumor-associated alpha carbonic anhydrases. Bioorganic & Medicinal Chemistry, 25(14), 3714−3718. google scholar
• • Lin, H. H., Wu, W. Y., Cao, S. L., Liao, J., Ma, L., Gao, M. ... Xu, X. (2013). Synthesis and antiproliferative evaluation of piperazine-1-carbothiohydrazide derivatives of indolin-2-one. Bioorganic & Medicinal Chemistry Letters, 23(11), 3304−3307. google scholar
• • Matesic, L., Locke, J. M., Bremner, J. B., Pyne, S. G., Skropeta, D., & Ranson, M. (2008). N-phenethyl and N-naphthylmethyl isatins and analogues as in vitro cytotoxic agents. Bioorganic & Medicinal Chemistry, 16, 3118−3124. google scholar
• • Mosmann, T. (1983). Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. Journal of Immunological Methods, 65, 55−63. google scholar
• • Pape, V. F. S., Tóth, S., Füredi, A., Szebényi, K., Lovrics, A., Szabó, P. … Szakács, G. (2016). Design, synthesis and biological evaluation of thiosemicarbazones, hydrazinobenzothiazoles and arylhydrazones as anticancer agents with a potential to overcome multidrug resistance. European Journal of Medicinal Chemistry, 117, 335−354. google scholar
• • Pervez, H., Saira, N., Iqbal, M. S., Yaqub, M., & Khan, K. M. (2011). Synthesis and toxicity evaluation of some N4-aryl substituted 5-trifluoromethoxyisatin-3-thiosemicarbazones. Molecules, 16(8), 6408−6421. google scholar
• • Pervez, H., Saira, N., Iqbal, M. S., Yaqub, M., & Khan, K. M. (2013). Synthesis and biological evaluation of some N 4-aryl-substituted 5-fluoroisatin-3-thiosemicarbazones. Medicinal Chemistry Research, 22(12), 5878−5889. google scholar
• • Priyanka, K. B., Manasa, C., & Sammaiah, G. (2014). Synthesis and evaluation of new isatin derivatives for cytotoxic activity. World Journal of Pharmacy and Pharmaceutical Sciences, 3, 2393−2402. • google scholar
• Raut, U., Narang, P., Mendiratta, D. K., Narang, R., & Deotale, V. (2008). Evaluation of rapid MTT tube method for detection of drug susceptibility of Mycobacterium tuberculosis to rifampicin and isoniazid. Indian Journal of Medical Microbiology, 26, 222−227. google scholar
• • Sabet, R., Mohammadpour, M., Sadeghi, A. & Fassihi, A. (2010). QSAR study of isatin analogues as in vitro anti-cancer agents, European Journal of Medicinal Chemistry, 45, 1113−1118. google scholar
• • Sevinçli, Z. Ş., Duran, G., Özbil, M., & Karalı, N. (2020). Synthesis, molecular modeling and antiviral activity of novel 5-fluoro-1Hindole- 2,3-dione 3-thiosemicarbazones. Bioorganic Chemistry, In press, https://doi.org/10.1016/j.bioorg.2020.104202 google scholar
• • Vine, K. L., Locke, J. M., Ranson, M., Pyne, S. G., & Bremner, J. B. (2007). An investigation into the cytotoxicity and mode of action of some novel N-alkyl-substituted isatins. Journal of Medicinal Chemistry, 50, 5109−5117. google scholar

Citations