Synthesis and Cytotoxic Activity of Arylsubstituted Tetrazolocyclanopyrimidines
- Autores: Vasil’kova N.O.1, Ivonin M.A.1, Burygin G.L.2, Prilepskii A.Y.2, Kriven’ko A.P.1
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Afiliações:
- N. G. Chernyshevskii Saratov State National Research University
- Institute of Plant and Microbial Biochemistry and Physiology
- Edição: Volume 51, Nº 9 (2017)
- Páginas: 756-759
- Seção: The Search for New Drugs
- URL: https://bakhtiniada.ru/0091-150X/article/view/244789
- DOI: https://doi.org/10.1007/s11094-017-1687-z
- ID: 244789
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Resumo
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.
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Sobre autores
N. Vasil’kova
N. G. Chernyshevskii Saratov State National Research University
Email: chem@folium.ru
Rússia, Saratov
M. Ivonin
N. G. Chernyshevskii Saratov State National Research University
Email: chem@folium.ru
Rússia, Saratov
G. Burygin
Institute of Plant and Microbial Biochemistry and Physiology
Email: chem@folium.ru
Rússia, Saratov
A. Prilepskii
Institute of Plant and Microbial Biochemistry and Physiology
Email: chem@folium.ru
Rússia, Saratov
A. Kriven’ko
N. G. Chernyshevskii Saratov State National Research University
Email: chem@folium.ru
Rússia, Saratov
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