Molecules
(Oct 2018)
Novel 5′-Norcarbocyclic Derivatives of Bicyclic Pyrrolo- and Furano[2,3-d]Pyrimidine Nucleosides
Anna A. Klimenko,
Elena S. Matyugina,
Evgeniya B. Logashenko,
Pavel N. Solyev,
Marina A. Zenkova,
Sergey N. Kochetkov,
Anastasia L. Khandazhinskaya
Affiliations
Anna A. Klimenko
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia
Elena S. Matyugina
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia
Evgeniya B. Logashenko
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of Russian Academy of Sciences, 8 Lavrentiev Ave., Novosibirsk 630090, Russia
Pavel N. Solyev
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia
Marina A. Zenkova
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of Russian Academy of Sciences, 8 Lavrentiev Ave., Novosibirsk 630090, Russia
Sergey N. Kochetkov
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia
Anastasia L. Khandazhinskaya
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia
DOI
https://doi.org/10.3390/molecules23102654
Journal volume & issue
Vol. 23,
no. 10
p.
2654
Abstract
Read online
Here we report the synthesis and biological activity of new 5′-norcarbocyclic derivatives of bicyclic pyrrolo- and furano[2,3-d]pyrimidines with different substituents in the heterocyclic ring. Lead compound 3i, containing 6-pentylphenyl substituent, displays inhibitory activity with respect to a number of tumor cells with a moderate selectivity index value. Compound 3i induces cell death by the apoptosis pathway with the dissipation of mitochondrial potential.
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