Silva, C.F.M., Guerrinha, A.P.D.d.M.S., Carvalho, S., Pinto, D.C.G.A., and Silva, A.M.S., 1,3,5-Triazine: A promising molecular scaffold for novel agents for the treatment of Alzheimer’s disease, Int. J. Mol. Sci., 2025, vol. 26, no. 3, p. 882. https://doi.org/10.3390/ijms26030882
Article CAS PubMed PubMed Central Google Scholar
Weixin, Y.A.N., Zhao, Y., and He, J., Anti‑breast cancer activity of selected 1,3,5‑triazines via modulation of EGFR‑TK, Mol. Med. Rep., 2018, vol. 18, no. 5, pp. 4175–4184. https://doi.org/10.3892/mmr.2018.9426
Srivastava, J.K., Pillai, G.G., Bhat, H.R., and Verma, A., Design and discovery of novel monastrol-1,3,5-triazines as potent anti-breast cancer agent via attenuating Epidermal Growth Factor Receptor tyrosine kinase, Sci. Rep., 2017, vol. 7, p. 5851. https://doi.org/10.1038/s41598-017-05934-5
Article CAS PubMed PubMed Central Google Scholar
Liu, B., A systematic review on antitumor agents with 1,3,5-triazines, Med. Chem. (Henderson, NV, U. S.), 2015, vol. 5, no. 3, pp. 131–148. https://doi.org/10.4172/2161-0444.1000255
Liu, B., A systematic review on antitumor agents with 1,3,5-triazines, Med. Chem. (Henderson, NV, U. S.), 2015, vol. 5, no. 3, pp. 131–148. https://doi.org/10.4172/2161-0444.1000255
Lim, H.Y. and Dolzhenko, A.V., 1,3,5-Triazine as a promising scaffold in the development of therapeutic agents against breast cancer, Eur. J. Med. Chem., 2024, vol. 276, p. 116680. https://doi.org/10.1016/j.ejmech.2024.116680
Article CAS PubMed Google Scholar
Mikolaichuk, O.V., Sharoyko, V.V., Popova, E.A., et al., A new tetrazole-containing 2-amino-4,6-di(aziridin-1-yl)-1,3,5-triazine derivative: Synthesis, interaction with DNA, and antitumor activity, Russ. Chem. Bull., 2022, vol. 71, pp. 1050–1056.
Marchesi, F., Turriziani, M., Tortorelli, G., Avvisati, G., Torino, F., and De Vecchis, L., Triazene compounds: Mechanism of action and related DNA repair systems, Pharmacol. Res., 2007, vol. 56, no. 4, pp. 275–287. https://doi.org/10.1016/j.phrs.2007.08.003
Article CAS PubMed Google Scholar
Andrés, C.M.C., de la Lastra, J.M.P., Juan, C.A., Plou, F.J., and Pérez-Lebeña, E., Chemical insights into oxidative and nitrative modifications of DNA, Int. J. Mol. Sci., 2023, vol. 24, no. 20, p. 15240. https://doi.org/10.3390/ijms242015240
Article CAS PubMed PubMed Central Google Scholar
Juvekar, A., Burga, L.N., Hu, H., et al., Combining a PI3K inhibitor with a PARP inhibitor provides an effective therapy for BRCA1-related breast cancer, Cancer Discovery, 2012, vol. 2, no. 11, pp. 1048–1063. https://doi.org/10.1158/2159-8290.CD-11-0336
Article CAS PubMed PubMed Central Google Scholar
Wang, J., Li, H., He, G., et al., Discovery of novel dual poly(ADP-ribose)polymerase and phosphoinositide 3-kinase inhibitors as a promising strategy for cancer therapy, J. Med. Chem., 2020, vol. 63, no. 1, pp. 122–139. https://doi.org/10.1021/acs.jmedchem.9b00622
Article CAS PubMed Google Scholar
Dai, Q. et al., Antitumor activity of s-triazine derivatives: A systematic review, Molecules, 2023, vol. 28, no. 11, p. 4278. https://doi.org/10.3390/molecules28114278
Article CAS PubMed PubMed Central Google Scholar
Protas, A.V. et al., Aziridine-functionalized 1,3,5-triazine derivatives as promising anticancer agents: Synthesis, DFT study, DNA binding investigations and in vitro cytotoxic activity, J. Heterocycl. Chem., 2024, vol. 61, no. 11, pp. 1801–1806. https://doi.org/10.1002/jhet.4908
Belyaeva, O.A. et al., Targeted delivery of domestic anticancer drugs from the group of aziridine triazines (literature review), Rev. Clin. Pharmacol. Drug Ther., 2024, vol. 22, no. 2, pp. 131–144. https://doi.org/10.17816/RCF625968
Molchanov, O.E. et al., Patent RU2825828C1, 2024.
Sharoyko, V.V. et al., Physicochemical investigation of water-soluble C60(C2NH4O2)4H4 (C60-Gly) adduct, J. Mol. Liq., 2021, vol. 344, p. 117658. https://doi.org/10.1016/j.molliq.2021.117658
Topala, T., Bodoki, A., Oprean, L., and Oprean, R., Experimental techniques employed in the study of metal complexes-DNA—interactions, Farmacia, 2014, vol. 62, pp. 1049–1061.
Can, Z., Keskin, B., Üzer, A., and Apak, R., Detection of nitric oxide radical and determination of its scavenging activity by antioxidants using spectrophotometric and spectrofluorometric methods, Talanta, 2022, vol. 238, no. 1, p. 122993. https://doi.org/10.1016/j.talanta.2021.122993
Ranjbari, S., Behzadi, M., Sepehri, S. et al., Investigations of antiproliferative and antioxidant activity of β-lactam morpholino-1,3,5-triazine hybrids, Bioorg. Med. Chem., 2020, vol. 28, no. 8, p. 115408. https://doi.org/10.1016/j.bmc.2020.115408
Article CAS PubMed Google Scholar
Mikolaichuk, O.V., Protas, A.V., Popova, E.A., Mukhametshina, A.V., Ovsepyan, G.K., and Trifonov, R.E., Quantitative studies of DNA binding with trans complexes of and PdII featuring tetrazolylacetic acids and their derivatives as ligands, Russ. Chem. Bull., 2018, vol. 67, no. 7, pp. 1312–1315.
Ali, I., Wani, W.A., Saleem, K., and Hsieh, M.-F., Anticancer metallodrugs of glutamic acid sulphonamides: In silico, DNA binding, hemolysis and anticancer studies, RSC Adv., 2014, vol. 4, no. 56, pp. 29629–29641. https://doi.org/10.1039/C4RA02570A
Karami, K., Alinaghi, M., Amirghofran, Z., and Lipkowski, J., Synthesis and characterization of two new trans palladium(II) complexes containing benzylamine ligand: DNA/BSA interactions, molecular docking and in vitro cytotoxic activity, Inorg. Chim. Acta, 2018, vol. 471, pp. 797–807. https://doi.org/10.1016/j.ica.2017.02.027
Gałczyńska, K., Ciepluch, K., Madej, Ł., et al., Selective cytotoxicity and antifungal properties of copper(II) and cobalt(II) complexes with imidazole-4-acetate anion or 1-allylimidazole, Sci. Rep., 2019, vol. 9, p. 9777. https://doi.org/10.1038/s41598-019-46224-6
Article CAS PubMed PubMed Central Google Scholar
Cao, Y. and He, X.-w., Studies of interaction between Safranine T and double helix DNA by spectral methods, Spectrochim. Acta, Part A, 1998, vol. 54, no. 6, pp. 883–892. https://doi.org/10.1016/S1386-1425(97)00277-1
Kessel, D., Luo, Y., Deng, Y., and Chang, C.K., The role of subcellular localization in initiation of apoptosis by photodynamic therapy, Photochem. Photobiol., 1997, vol. 65, no. 3, pp. 422–426. https://doi.org/10.1111/j.1751-1097.1997.tb08581.x
Article CAS PubMed PubMed Central Google Scholar
Pierce, A., McGowan, P.M., Cotter, M., et al., Comparative antiproliferative efects of iniparib and olaparib on a panel of triple-negative and non-triple-negative breast cancer cell lines, Cancer Biol. Ther., 2013, vol. 14, no. 6, pp. 537–545. https://doi.org/10.4161/cbt.24349
Article CAS PubMed PubMed Central Google Scholar
Molla, S., Hembram, K.C., Chatterjee, S., et al., PARP inhibitor Olaparib enhances the apoptotic potentiality of curcumin by increasing the DNA damage in oral cancer cells through inhibition of BER cascade, Pathol. Oncol. Res., 2020, vol. 26, no. 4, pp. 2091–2103. https://doi.org/10.1007/s12253-019-00768-0
Comments (0)