Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yana R. Orshanskaya"'
Autor:
Nariman F. Salakhutdinov, Olga I. Yarovaya, Anna A. Shtro, Kseniya S. Kovaleva, Andrey V. Shernyukov, Yana R. Orshanskaya, Vladimir V. Zarubaev
Publikováno v:
Chemistry of Heterocyclic Compounds. 53:364-370
New derivatives of dehydroabietylamine were obtained by transformation of primary amino group to pyrrolidine, piperidine, azepane, morpholine, isoindoline, and pyrrole heterocycles. The obtained compounds were tested for antiviral activity against in
Autor:
A. E. Ivanova, Vladimir V. Zarubaev, Viktor I. Saloutin, Yanina V. Burgart, Yana R. Orshanskaya
Publikováno v:
Mendeleev Communications. 28:52-54
Regiospecific ribosylation of 3-polyfluoroalkyl-5-phenylpyrazoles with 1,2,3,5-tetra-O-acetyl-β-d-ribofuranose in the presence of tin(iv) chloride followed by deacetylation affords 1-(β-d-ribofuranosyl)-3-polyfluoroalkyl-5-phenyl- 1H-pyrazoles. The
Autor:
Nariman F. Salakhutdinov, Konstantin P. Volcho, Svetlana Yu. Kurbakova, Oksana S. Patrusheva, Sergey A. Boldyrev, Yana R. Orshanskaya, Vladimir V. Zarubaev, Dina V. Korchagina, Irina V. Ilyina, Anna A. Shtro
Publikováno v:
Bioorganicmedicinal chemistry. 24(21)
The antiviral activity of 4-hydroxy-hexahydro-2H-chromenes and 4-fluorine-hexahydro-2H-chromenes with an aromatic substituent, synthesized from monoterpene (-)-verbenone, was studied for the first time. Five of 11 (45 per cent) of 4-hydroxy-hexahydro
Autor:
Nariman F. Salakhutdinov, Vlad A Korobeynikov, Sergey V. Cheresiz, Andrey G. Pokrovsky, Olga I. Yarovaya, Yana R. Orshanskaya, Vladimir V. Zarubaev, Kseniya S. Kovaleva, A. A. Kononova, Anna A. Shtro
Publikováno v:
Medicinal chemistry. 6
Here, we report the synthesis of a series of dehydroabietylamine (DAA) salts. We studied the cytotoxic activity of DAA salts and their and antiviral properties against influenza virus A(H1N1)pdm09 We further compared these parameters to those of DAA
Autor:
Vladimir V. Zarubaev, Elza Karimova, Tagir Gabbasov, Yana R. Orshanskaya, Leonid V. Spirikhin, Lidia A. Baltina
Publikováno v:
Natural Product Communications. 10:1934578X1501000
Reaction of quercetin (QR) (1) with bromine under various conditions was studied. Interaction of QR with 2–3 equiv. of bromine in glacial acetic acid at 35–40°C for 2–4 h and 20–22°C for 24 h led to the formation of QR 6,8-dibromide (2) (52