Synthesis, Characterization, and Evaluation of MCF-7 (Breast Cancer) for Schiff, Mannich Bases, and Their Complexes
Ali Mudher Abdulkareem Al-Khazraji(1*)
(1) Department of Chemistry, College of Education for Pure Science Ibn Al-Haitham, University of Baghdad, Baghdad 10011, Iraq
(*) Corresponding Author
Abstract
Keywords
Full Text:
Full Text PDFReferences
[1] Wei, L., Chang, X., and Wang, C.J., 2020, Catalytic asymmetric reactions with N-metallated azomethine ylides, Acc. Chem. Res., 53 (5), 1084–1100.
[2] Raczuk, E., Dmochowska, B., Samaszko-Fiertek, J., and Madaj, J., 2022, Different Schiff bases—Structure, importance and classification, Molecules, 27 (3), 787.
[3] Al-Khazraji, A.M., and Al Hassani, R.A., 2020, Synthesis, characterization and spectroscopic study of new metal complexes form heterocyclic compounds for photostability study, Sys. Rev. Pharm., 11 (5), 535–555.
[4] Abd Razak, N., Abu, N., Ho, W.Y., Zamberi, N.R., Tan, S.W., Alitheen, N.B., Long, K., and Yeap, S.K., 2019, Cytotoxicity of eupatorin in MCF-7 and MDA-MB-231 human breast cancer cells via cell cycle arrest, anti-angiogenesis and induction of apoptosis, Sci. Rep., 9 (1), 1514.
[5] Lindhagen, E., Nygren, P., and Larsson, R., 2008, The fluorometric microculture cytotoxicity assay, Nat. Protoc., 3 (8), 1364–1369.
[6] Al-Khazraji, A.M.A., 2023, Synthesis of Co(II), Ni(II), Cu(II), Pd(II), and Pt(IV) complexes with 14,15,34,35-tetrahydro-11H,31H-4,8-diaza-1,3(3,4)-ditriazola-2,6(1,4)-dibenzenacyclooctaphane-4,7-dien-15,35-dithione, and the thermal stability of polyvinyl chloride modified complexes, Indones. J. Chem., 23 (3), 754–769.
[7] Al-Ezzy, R.M., Alshanon, A.F., and Khalaf, H.M., 2023, Studying some cytotoxic and cytogenetic potentials of Dandelion methanolic extract on MCF-7 cancer cell line: An in vitro study, Iraqi J. Sci., 64 (3), 1160–1170.
[8] Baldwin, E.L., and Osheroff, N., 2005, Etoposide, topoisomerase II and cancer, Curr. Med. Chem.: Anti-Cancer Agents, 5 (4), 363–372.
[9] Fusco, R., Cordaro, M., Siracusa, R., Peritore, A.F., D’Amico, R., Licata, P., Crupi, R., and Gugliandolo, E., 2020, Effects of hydroxytyrosol against lipopolysaccharide-induced inflammation and oxidative stress in bovine mammary epithelial cells: A natural therapeutic tool for bovine mastitis, Antioxidants, 9 (8), 693.
[10] Wang, H., and Mao, X., 2020, Evaluation of the efficacy of neoadjuvant chemotherapy for breast cancer, Drug Des., Dev. Ther., 14, 2423–2433.
[11] Aswathanarayanappa, C., Bheemappa, E., Bodke, Y.D., Krishnegowda, P.S., Venkata, S.P., and Ningegowda, R., 2013, Synthesis and evaluation of antioxidant properties of novel 1,2,4‐triazole‐based Schiff base heterocycles, Arch. Pharm., 346 (12), 922–930.
[12] Seelam, N., Shrivastava, S., Prasanthi, S., and Gupta, S., 2016, Synthesis and in vitro study of some fused 1,2,4-triazole derivatives as antimycobacterial agents, J. Saudi Chem. Soc., 20 (4), 411–418.
[13] Lehrich, B.M., Liang, Y., and Fiandaca, M.S., 2021, Foetal bovine serum influence on in vitro extracellular vesicle analyses, J. Extracell. Vesicles, 10 (3), e12061.
[14] Tamer, T.M., Sabet, M.M., Omer, A.M., Abbas, E., Eid, A.I., Mohy-Eldin, M.S., and Hassan, M.A., 2021, Hemostatic and antibacterial PVA/Kaolin composite sponges loaded with penicillin–streptomycin for wound dressing applications, Sci. Rep., 11 (1), 3428.
[15] Vajta, G., and Kuwayama, M., 2006, Improving cryopreservation systems, Theriogenology, 65 (1), 236–244.
[16] Al-Khazraji, A.M., Al Hassani, R.A., and Ahmed, A., 2020, Studies on the photostability of polystyrene films with new metals complex of 1,2,4-triazole-3-thione derivate, Sys. Rev. Pharm., 11 (5), 525–534.
[17] Hozien, Z.A., El-Mahdy, A.F., Abo Markeb, A., Ali, L.S.A., and El-Sherief, H.A.H., 2020, Synthesis of Schiff and Mannich bases of new s-triazole derivatives and their potential applications for removal of heavy metals from aqueous solution and as antimicrobial agents, RSC Adv., 10 (34), 20184–20194.
[18] Hossain, N., Zaini, J., Mahlia, T., and Azad, A.K., 2019, Elemental, morphological and thermal analysis of mixed microalgae species from drain water, Renewable Energy, 131, 617–624.
[19] Pérez, S., Montalbán, M.G., Carissimi, G., Licence, P., and Víllora, G., 2020, In vitro cytotoxicity assessment of monocationic and dicationic pyridinium-based ionic liquids on HeLa, MCF-7, BGM and EA.hy926 cell lines, J. Hazard. Mater., 385, 121513.
[20] Casaos, J., Gorelick, N.L., Huq, S., Choi, J., Xia, Y., Serra, R., Felder, R., Lott, T., Kast, R.E., Suk, I., Brem, H., Tyler, B., and Skuli, N., 2019, The use of ribavirin as an anticancer therapeutic: Will it go viral?, Mol. Cancer Ther., 18 (7), 1185–1194.
[21] Ianevski, A., Yao, R., Biza, S., Zusinaite, E., Mannik, A., Kivi, G., Planken, A., Kurg, K., Tombak, E.M., Ustav, Jr. M., Shtaida, N., Kulesskiy, E., Jo, E., Yang, J., Lysvand, H., Løseth, K., Oksenych, V., Aas, P.A., Tenson, T., Vitkauskienė, A., Windisch, M.P., Fenstad, M.H., Nordbø, S.A., Ustav, M., Bjørås, M., and Kainov, D.E., 2020, Identification and tracking of antiviral drug combinations, Viruses, 12 (10), 1178.
[22] El-Sheridy, N.A., El-Moslemany, R.M., Ramadan, A.A., Helmy, M.W., and El-Khordagui, L.K., 2021, Enhancing the in vitro and in vivo activity of itraconazole against breast cancer using miltefosine-modified lipid nanocapsules, Drug Delivery, 28 (1), 906–919.
[23] Li, L., Gao, B., Wen, Y., Zhang, Z., Chen, R., He, Z., Kaziem, A.E., Shi, H., and Wang, M., 2020, Stereoselective bioactivity, toxicity and degradation of the chiral triazole fungicide bitertanol, Pest. Manage. Sci., 76 (1), 343–349.
[24] Yang, F.W., Li, Y.X., Ren, F.Z., Wang, R., and Pang, G.F., 2019, Toxicity, residue, degradation and detection methods of the insecticide triazophos, Environ. Chem. Lett., 17 (4), 1769–1785.
[25] Deepthi, A., Thomas, N.V., and Sruthi, S.L., 2021, An overview of the reactions involving azomethine imines over half a decade, New J. Chem., 45 (20), 8847–8873.
[26] Barreca, M., Stathis, A., Barraja, P., Bertoni, F., 2020, An overview on anti-tubulin agents for the treatment of lymphoma patients, Pharmacol. Ther., 211, 107552.
[27] Ciapetti, G., Cenni, E., Pratelli, L., and Pizzoferrato, A., 1993, In vitro evaluation of cell/biomaterial interaction by MTT assay, Biomaterials, 14 (5), 359–364.
[28] Xu, X., Lai, Y., and Hua, Z.C., 2019, Apoptosis and apoptotic body: Disease message and therapeutic target potentials, Biosci. Rep., 39 (1), BSR20180992.
[29] Olmsted III, J., and Kearns, D.R., 1977, Mechanism of ethidium bromide fluorescence enhancement on binding to nucleic acids, Biochemistry, 16 (16), 3647–3654.
[30] Fischer, E.G., 2020, Nuclear morphology and the biology of cancer cells, Acta Cytol., 64 (6), 511–519.
DOI: https://doi.org/10.22146/ijc.87003
Article Metrics
Abstract views : 1673 | views : 1455Copyright (c) 2023 Indonesian Journal of Chemistry
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Indonesian Journal of Chemistry (ISSN 1411-9420 /e-ISSN 2460-1578) - Chemistry Department, Universitas Gadjah Mada, Indonesia.
View The Statistics of Indones. J. Chem.