Brodowska, K. and Łodyga-Chruścińska, E., Schiff’s principles—An interesting range of applications in various fields of science, Chemist, 2014, vol. 68, no. 2.
Salihović, M., Pazalja, M., Mahmutović-Dizdarević, I., Jerković-Mujkić, A., Suljagić, J., Špirtović-Halilović, S., and Šapčanin, A., Synthesis, DFT study and antimicrobial activity of Schiff bases derived from benzaldehydes and amino acids, Rasayan J. Chem., 2018, vol. 11, no. 3, pp. 1074–1083. https://doi.org/10.31788/RJC.2018.1133077
Tahriri, M., Yousefi, M., Mehrani, K., Tabata-baee, M., and Ashkezari, M.D., Synthesis, characterization and antimicrobial activity of two novel sulfonamide Schiff base compounds, Pharm. Chem. J., 2017, vol. 51, pp. 425–428.https://doi.org/10.1007/s11094-017-1626-z
Ceramella, J., Iacopetta, D., Catalano, A., Cirillo, F., Lappano, R., and Sinicropi, M.S., A review on the antimicrobial activity of Schiff bases: Data collection and recent studies, Antibiotics, 2022, vol. 11, no. 2, p. 191. https://doi.org/10.3390/antibiotics11020191
Article CAS PubMed PubMed Central Google Scholar
Hassan, A.S., Awad, H.M., Magd-El-Din, A.A., and Hafez, T.S., Synthesis and in vitro antitumor evaluation of novel Schiff bases, Med. Chem. Res., 2018, vol. 27, pp. 915–927. https://doi.org/10.1007/s00044-017-2113-5
Kumar, M., Padmini, T., and Ponnuvel, K., Synthesis, characterization and antioxidant activities of Schiff bases are of cholesterol, J. Saudi Chem. Soc., 2017, vol. 21, pp. S322–S328. https://doi.org/10.1016/j.jscs.2014.03.006
Luo, H., Yang, S., Cai, Y., Peng, Z., and Liu, T., Synthesis and biological evaluation of novel 6-chloro-quinazolin derivatives as potential antitumor agents, Eur. J. Med. Chem., 2014, vol. 84, pp. 746–752. https://doi.org/10.1016/j.ejmech.2014.07.053
Article CAS PubMed Google Scholar
Panneerselvam, P., Rather, B.A., Reddy, D.R.S., and Kumar, N.R., Synthesis and anti-microbial screening of some Schiff bases of 3-amino-6,8-dibromo-2-phenylquinazolin-4(3H)-ones, Eur. J. Med. Chem., 2009, vol. 44, no. 5, pp. 2328–2333. https://doi.org/10.1016/j.ejmech.2008.04.010
Article CAS PubMed Google Scholar
Jin, X., Wang, J., and Bai, J., Synthesis and antimicrobial activity of the Schiff base from chitosan and citral, Carbohydr. Res., 2009, vol. 344, no. 6, pp. 825–829. https://doi.org/10.1016/j.carres.2009.01.022
Article CAS PubMed Google Scholar
Bharti, S.K., Nath, G., Tilak, R., and Singh, S.K., Synthesis, anti-bacterial and anti-fungal activities of some novel Schiff bases containing 2,4-disubstituted thiazole ring, Eur. J. Med. Chem., 2010, vol. 45, no. 2, pp. 651–660. https://doi.org/10.1016/j.ejmech.2009.11.008
Article CAS PubMed Google Scholar
Aytac, S., Gundogdu, O., Bingol, Z., and Gulcin, İ., Synthesis of Schiff bases containing phenol rings and investigation of their antioxidant capacity, anticholinesterase, butyrylcholinesterase, and carbonic anhydrase inhibition properties, Pharmaceutics, 2023, vol. 15, no. 3, p. 779. https://doi.org/10.3390/pharmaceutics15030779
Article CAS PubMed PubMed Central Google Scholar
Nawaz, H., Akhter, Z., Yameen, S., Siddiqi, H.M., Mirza, B., and Rifat, A., Synthesis and biological evaluations of some Schiff-base esters of ferrocenyl aniline and simple aniline, J. Organomet. Chem., 2009, vol. 694, no. 14, pp. 2198–2203. https://doi.org/10.1016/j.jorganchem.2009.02.032
Beč, A., Cindrić, M., Persoons, L., Banjanac, M., Radovanović, V., Daelemans, D., and Hranjec, M., Novel biologically active N-substituted benzimidazole derived Schiff bases: Design, synthesis, and biological evaluation, Molecules, 2023, vol. 28, no. 9, p. 3720. https://doi.org/10.3390/molecules28093720
Article CAS PubMed PubMed Central Google Scholar
Reshma, R., Selwin Joseyphus, R., Arish, D., Reshmi Jaya, R.J., and Johnson, J., Tridentate imidazole-based Schiff base metal complexes: Molecular docking, structural and biological studies, J. Biomol. Struct. Dyn., 2022, vol. 40, no. 18, pp. 8602–8614. https://doi.org/10.1080/07391102.2021.1914171
Article CAS PubMed Google Scholar
Da Silva, C.M., da Silva, D.L., Modolo, L.V., Alves, R.B., de Resende, M.A., Martins, C.V., and de Fátima, Â., Schiff bases: A short review of their antimicrobial activities, J. Adv. Res., 2011, vol. 2, no. 1, pp. 1–8. https://doi.org/10.1016/j.jare.2010.05.004
Bringmann, G., Dreyer, M., Faber, J.H., Dalsgaard, P.W., Stærk, D., Jaroszewski, J.W., et al., Ancistrotanzanine C and related 5,1'-and 7,3'-coupled Naphthylisoquinoline alkaloids from Ancistrocladus tanzaniensis, J. Nat. Prod., 2004, vol. 67, no. 5, pp. 743–748. https://doi.org/10.1021/np0340549
Article CAS PubMed Google Scholar
Souza, A.O.D., Galetti, F., Silva, C.L., Bicalho, B., Parma, M.M., Fonseca, S.F., et al., Antimycobacterial and cytotoxicity activity of synthetic and natural compounds, Quím. Nova, 2007, vol. 30, pp. 1563–1566. https://doi.org/10.1590/S0100-40422007000700012
Guo, Z., Xing, R., Liu, S., Zhong, Z., Ji, X., Wang, L., and Li, P., Antifungal properties of Schiff bases of chitosan, N-substituted chitosan and quaternized chitosan, Carbohydr. Res., 2007, vol. 342, no. 10, pp. 1329–1332. https://doi.org/10.1016/j.carres.2007.04.006
Article CAS PubMed Google Scholar
Mensah, S., Syntheses, Characterization, and Preliminary Evaluation of Potential Ruthenium Anticancer Complexes Containing Schiff Base Ligands, Illinois State University, 2019.
Desai, N.C., Shihora, P.N., and Moradia, D.L., Synthesis and characterization of new quinazolines as potential antimicrobial agents, ChemInform, 2007, vol. 38, no. 29.
Patel, A.B., Synthesis of hot brand reactive dyes based on 4,4'-methylene bis(2-fluoro aniline) and their application on various fibres, Int. J. Creative Res. Thoughts, 2023, vol. 11, no. 11, pp. 513–521.
Patel, P.C., Rana, U.R., Patel, K.C., and Patel, S.K., Synthesis and evaluation of a series of symmetrical hot brand bis azo reactive dyes using 4,4′-methylene-bis-metanilic acid on various fibre, Asian J. Chem., 2002, vol. 14, no. 1, p. 265.
Wayne, P.A., National Committee for Clinical Laboratory Standards, Reference method for broth dilution antifungal susceptibility testing of yeasts, Off. J. Eur. Union, 2022, vol. 28, no. 14.
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