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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2021 Volume 31, Issue 3, Pages 288–290 (Mi mendc907)

This article is cited in 6 papers

Communications

N-(4-Methoxyphenyl)-substituted bicyclic isothioureas: effect on morphology of cancer cells

A. V. Evdokimovaa, A. A. Alexeeva, E. V. Nurievaa, E. R. Milaevaab, S. A. Kuznetsovc, O. N. Zefirovaab

a Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
b Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, Chernogolovka, Moscow Region, Russian Federation
c Institute of Biological Sciences, Cell Biology and Biosystems Technology, University of Rostock, Rostock, Germany

Abstract: Bicyclic isothioureas of N-(4-methoxyphenyl)-2-aminocycloalkane[d]thiazole type were obtained using intramolecular electrophilic cyclization of N-(cycloalk-2-enyl)-N′-(4-methoxyphenyl)thioureas. Isothiourea fused with sevenmembered ring caused noticeable changes of the morphology of human lung carcinoma cells A549, but without affecting their microtubule net.

Keywords: thiazolin-2-amines, cycloalka[d]thiazoles, thioureas, isothioureas, heterocyclization, verubulin, lung carcinoma A549, cancer cell morphology.

Language: English

DOI: 10.1016/j.mencom.2021.04.003



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