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Mendeleev Communications, 2024, Volume 34, Issue 6, Pages 859–861
DOI: https://doi.org/10.1016/j.mencom.2024.10.028
(Mi mendc273)
 

Communications

Synthesis, physicochemical properties and in vitro cytotoxic activity of aziridine-containing derivatives of 1,3,5-triazine

O. V. Mikolaichukab, A. V. Protasab, E. A. Popovaab, O. S. Shemchuka, M. D. Luttseva, D. R. Dadadzhanovc, T. A. Vartanyanc, A. V. Petrovd, V. V. Sharoykoabd, K. N. Semenovabd, O. E. Molchanovb, D. N. Maistrenkob

a I.P. Pavlov First St. Petersburg State Medical University, St. Petersburg, Russian Federation
b A.M. Granov Russian Research Center for Radiology and Surgical Technologies, St. Petersburg, Russian Federation
c Infochemistry Scientific Center, ITMO University, St. Petersburg, Russian Federation
d Institute of Chemistry, St. Petersburg State University, St. Petersburg, Russian Federation
Abstract: 6-{[4-(Aziridin-1-yl)-6-chloro-1,3,5-triazin-2-yl]amino}-hexanoic acid methyl ester and sodium salt were synthesized from cyanuric chloride. The sodium salt would interact with free radicals of 2,2-diphenyl-1-picrylhydrazyl (DPPH) and inhibit hemolysis induced by Radachlorin. Both compounds interact with DNA with Kbin values of 1.09 × 107 and 0.99 × 107 dm3 mol−1, respectively; they also demonstrate cytotoxic activity against human cancer cell lines.
Keywords: 1,3,5-triazine, aziridine, cyanuric chloride, imidazo[1,2-a][1,3,5]triazine, physicochemical properties, biocompatibility, interaction with DNA, cytotoxic activity.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (830.4 Kb)


Citation: O. V. Mikolaichuk, A. V. Protas, E. A. Popova, O. S. Shemchuk, M. D. Luttsev, D. R. Dadadzhanov, T. A. Vartanyan, A. V. Petrov, V. V. Sharoyko, K. N. Semenov, O. E. Molchanov, D. N. Maistrenko, “Synthesis, physicochemical properties and in vitro cytotoxic activity of aziridine-containing derivatives of 1,3,5-triazine”, Mendeleev Commun., 34:6 (2024), 859–861
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