Zobrazeno 1 - 5
of 5
pro vyhledávání: '"5′-norcarbocyclic nucleoside analogues"'
Autor:
Vasily A. Kezin, Elena S. Matyugina, Mikhail S. Novikov, Alexander O. Chizhov, Robert Snoeck, Graciela Andrei, Sergei N. Kochetkov, Anastasia L. Khandazhinskaya
Publikováno v:
Molecules, Vol 27, Iss 9, p 2866 (2022)
Pyrimidine nucleoside analogues are widely used to treat infections caused by the human immunodeficiency virus (HIV) and DNA viruses from the herpes family. It has been shown that 5-substituted uracil derivatives can inhibit HIV-1, herpes family viru
Externí odkaz:
https://doaj.org/article/ba7d97f4d9c742ed9afcdcc355080063
Autor:
Anna A. Klimenko, Elena S. Matyugina, Evgeniya B. Logashenko, Pavel N. Solyev, Marina A. Zenkova, Sergey N. Kochetkov, Anastasia L. Khandazhinskaya
Publikováno v:
Molecules, Vol 23, Iss 10, p 2654 (2018)
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 substituen
Externí odkaz:
https://doaj.org/article/bd62b854daba4f88b774317fef51845e
Akademický článek
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Autor:
Sergey N. Kochetkov, Marina A. Zenkova, Evgeniya B. Logashenko, Anna A. Klimenko, Anastasia L. Khandazhinskaya, Pavel N. Solyev, Elena S. Matyugina
Publikováno v:
Molecules
Volume 23
Issue 10
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules, Vol 23, Iss 10, p 2654 (2018)
Volume 23
Issue 10
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules, Vol 23, Iss 10, p 2654 (2018)
Here we report the synthesis and biological activity of new 5&prime
norcarbocyclic derivatives of bicyclic pyrrolo- and furano[2,3-d]pyrimidines with different substituents in the heterocyclic ring. Lead compound 3i, containing 6-pentylphenyl su
norcarbocyclic derivatives of bicyclic pyrrolo- and furano[2,3-d]pyrimidines with different substituents in the heterocyclic ring. Lead compound 3i, containing 6-pentylphenyl su
Autor:
Klimenko AA; Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia. kanna76v@gmail.com., Matyugina ES; Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia. matyugina@gmail.com., Logashenko EB; Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of Russian Academy of Sciences, 8 Lavrentiev Ave., Novosibirsk 630090, Russia. evg_log@ngs.ru., Solyev PN; Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia. solyev@gmail.com., Zenkova MA; Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of Russian Academy of Sciences, 8 Lavrentiev Ave., Novosibirsk 630090, Russia. marzen@niboch.nsc.ru., Kochetkov SN; Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia. kochet@eimb.ru., Khandazhinskaya AL; Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia. khandazhinskaya@bk.ru.
Publikováno v:
Molecules (Basel, Switzerland) [Molecules] 2018 Oct 16; Vol. 23 (10). Date of Electronic Publication: 2018 Oct 16.