[5]
Egbujor, M.C.; Nwobodo, D.C.; Egwuatu, P.I.; Abu, I.P.; Ezeagu, C.U. Sulphonamide drugs and pseudomonas aeruginosa resistance: A review. Int. J. Modern Pharm. Res., 2020, 4(1), 78-83.
[16]
Deepa, S.J.; Saravanan, R.E.; Praveen, T.K. An update on the role of Nrf2 and its activators in diseases associated with oxidative stress. Indian J. Pharm. Sci., 2020, 82(2), 1-10.
[18]
Halliwell, B.; Gutteridge, J.M.C. Free radicals in biology and medicine, 4th ed; Clarendon Press: Oxford, UK, 2007.
[32]
Fridovich, I. Free radicals in biology; Academic press: New York, 1976.
[38]
Moureu, C.; Dufraisse, C. Sur l’autoxydation: Les antioxygènes. Comptes Rendus des Séances et Mémories de la Société de Biologie, 1922, 86, 321-322. [in French]
[42]
Kuciel-lewandowska, J.; Kasperczak, M.; Bogut, B.; Heider, R. laber, W.T.; laber, W.; Paprocka-Borowicz, M. The impact of health resort treatment on the non-enzymatic endogenous antioxidant system. Oxid. Med. Cell. Longev., 2020.
[57]
Porcheddu, A.; De Lucca, L. Microwave-assisted synthesis of sulfonamides. Future Science Book Series, Microwaves in drug discovery and development: Recent advances; John Spencer & Mark Bogley, Future Science, 2014.
[70]
Hartwig, J.F. Organotransition metal chemistry: From bonding to catalysis; University Science Books, 2010.
[71]
Kim, J-G.; Jang, D.O. Mild and efficient indium metal catalyzed synthesis of sulfonamides and sulfonic esters. Synlett, 2007, 16, 2501-2504.
[80]
Torok, B.; Dransfield, T. Green Chemistry: An Inclusive Approach; Elsevier: Amsterdam, Netherlands, 2018.
[88]
Rehman, H.; Quadir, A.; Ali, Z.; Nazir, S.; Zahra, A.; Shahzady, T.G. Synthesis and characterization of novel sulfonamide derivatives and their antimicrobial, antioxidant and cytotoxicity evaluation. Bull. Chem. Soc. Ethiop., 2017, 31(3), 391-398.
[89]
Askar, F.W.; Aldhalf, Y.A.; Jinzeel, N.A.; Nief, O.A. Synthesis and biological evaluation of new sulfonamide derivatives. Int. J. Chem. Sci., 2017, 15(3), 173.
[93]
Al-Atbi, H.S.; Al-Salami, B.K.; Al-Assadi, I.J. New azoazomethine derivatives of sulfonamide: Synthesis, characterization, spectroscopic, antimicrobial and antioxidant activity study IOP Conf. Series: Journal of Physics: Conf. Series,, 2019, 1294, p. 052033.
[94]
Akocak, S.; Boga, M.; Lolak, N.; Tuneg, M.; Sanku, R.K.K. Design, synthesis and biological evaluation of 1,3-diaryltriazene-substituted sulfonamides as antioxidant, acetylcholinestrase and butyrylcholinesterase inhibitors. J. Turkish Chem. Soc, 2019, 6(1), 63-70.
[97]
Egbujor, M.C.; Okoro, U.C.; Okafor, S.; Nwankwo, N.E. Design, synthesis and molecular docking of novel serine-based sulphonamide bioactive compounds as potential antioxidant and antimicrobial agents. J. Pharm. Sci., 2019, 06(06), 12232-12240.
[118]
Tomoyo, M.; Shinnosuke, M.; Yka, O. Nrf2-activating compound.
WO/2021/002473, 2021.
[119]
Roy, K.; Kar, S. Das, RN Chapter 1.2: What is QSAR? Definitions and formulism A primer on QSAR/QSPR modelling: Fundamental concepts.Springer-Verlag Inc: New York, , 2015; pp. 2-6.
[122]
Natasenamat, C.; Isarankura, N.; Ayudhya, C.; Naenna, T.; Prachayasi, V.A. Practical overview of quantitative structure activity relationship. EXCLI J., 2009, 8, 74-88.
[124]
Egbujor, M.C.; Okoro, U.C.; Okafor, S.; Nwankwo, N.E. Synthesis, characterization and in silico studies of novel alkanoylated 4-methylphenyl sulphonamoyl carboxylic acids as potential antimicrobial and antioxidant agents. Intern. J. Pharm. Phytopharm. Res, 2019, 9(3), 89-97.