Synthesis and Cytotoxic Activity of Arylsubstituted Tetrazolocyclanopyrimidines


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Abstract

A series of arylsubstituted tetrazolocyclanodihydropyrimidines was prepared and their cytotoxic actions on SPEV-2 cells were studied. The activity of these substances was found to depend on the nature and position of the substitution groups in the benzene ring and the size of the alicycle. The most active compounds were o-chloro(methyl)phenyltetrazolohexahydroquinazolines.

About the authors

N. O. Vasil’kova

N. G. Chernyshevskii Saratov State National Research University

Email: chem@folium.ru
Russian Federation, Saratov

M. A. Ivonin

N. G. Chernyshevskii Saratov State National Research University

Email: chem@folium.ru
Russian Federation, Saratov

G. L. Burygin

Institute of Plant and Microbial Biochemistry and Physiology

Email: chem@folium.ru
Russian Federation, Saratov

A. Yu. Prilepskii

Institute of Plant and Microbial Biochemistry and Physiology

Email: chem@folium.ru
Russian Federation, Saratov

A. P. Kriven’ko

N. G. Chernyshevskii Saratov State National Research University

Email: chem@folium.ru
Russian Federation, Saratov


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