Biological activity of some sulfur- and selenium-containing spiro compounds


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Abstract

Cytotoxicity to K-562 leukemia cell line of two spiro compounds containing selenium or sulfur atom in their structure were compared. 4-Fluorophenyl-(1-thia-3-azaspiro[5.5]undec-2-en-2-yl]amine hydrobromide was synthesized and characterized for the first time. It was found that the introduction of a sulfur atom is more promising for this biological model, since it leads to a 3-fold increase in the therapeutic index in the case of the sulfur-containing compound.

About the authors

A. N. Proshin

Institute of Physiologically Active Compounds, Russian Academy of Sciences

Email: orlova.radiochem@mail.ru
Russian Federation, 1 Severnyi pr-d, Chernogolovka, Moscow Region, 142432

M. A. Orlova

Department of Chemistry, M. V. Lomonosov Moscow State University; Dmitry Rogachev National Scientific-Clinical Center of Pediatric Hematology, Oncology, and Immunology

Author for correspondence.
Email: orlova.radiochem@mail.ru
Russian Federation, Build. 3, 1 Leninskie Gory, Moscow, 119991; I ul. Samory Mashela, Moscow, 117997

T. P. Trofimova

Department of Chemistry, M. V. Lomonosov Moscow State University; Dmitry Rogachev National Scientific-Clinical Center of Pediatric Hematology, Oncology, and Immunology

Email: orlova.radiochem@mail.ru
Russian Federation, Build. 3, 1 Leninskie Gory, Moscow, 119991; I ul. Samory Mashela, Moscow, 117997

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