Zobrazeno 1 - 10
of 111
pro vyhledávání: '"I Yu Chukicheva"'
Autor:
I. Yu. Chukicheva, E. V. Buravlev, I. A. Dvornikova, I. V. Fedorova, V. V. Zarubaev, A. V. Slita, Ya. L. Esaulkova, A. V. Kutchin
Publikováno v:
Russian Chemical Bulletin. 71:2473-2481
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::813c8ce08383db5d3085674d95b170a3
https://doi.org/10.1007/s11172-022-3676-y
https://doi.org/10.1007/s11172-022-3676-y
Publikováno v:
Russian Chemical Bulletin. 71:2383-2394
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43013d107e905c54c10e7977c07ce685
https://doi.org/10.1007/s11172-022-3666-0
https://doi.org/10.1007/s11172-022-3666-0
Autor:
T. G. Borovskaya, A. V. Vychuzhanina, Yu. A. Shchemerova, E. V. Buravlev, I. Yu. Chukicheva, A. V. Kuchin
Publikováno v:
Bulletin of Experimental Biology and Medicine. 173:714-718
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82b83ca12c4f3e1bdfbc3ab1250e6feb
https://doi.org/10.1007/s10517-022-05618-9
https://doi.org/10.1007/s10517-022-05618-9
Autor:
L. I. Mazaletskaya, N. I. Sheludchenko, L. N. Shishkina, I. Yu. Chukicheva, E. V. Buravlev, O. V. Shchukina, A. V. Kutchin
Publikováno v:
Russian Journal of Physical Chemistry A. 96:964-968
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fffd03dce172e94de73aeb01d5f4b383
https://doi.org/10.1134/s0036024422050211
https://doi.org/10.1134/s0036024422050211
Publikováno v:
Theoretical and Applied Ecology. :26-33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43751f4b34b0c9688c6333d7c4ae235c
https://doi.org/10.25750/1995-4301-2022-3-026-033
https://doi.org/10.25750/1995-4301-2022-3-026-033
Publikováno v:
Russian Chemical Bulletin. 70:2185-2188
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a151efb612229a77df54eda755569258
https://doi.org/10.1007/s11172-021-3330-0
https://doi.org/10.1007/s11172-021-3330-0
Autor:
Galina A. Chernysheva, T. M. Plotnikova, V. I. Smol’yakova, I. Yu. Chukicheva, Anton N. Osipenko, A. V. Kutchin
Publikováno v:
Bulletin of Experimental Biology and Medicine. 169:310-313
2,6-Diisobornyl-4-methylphenol (Dibornol, 10 mg/kg intragastrically daily for 5 days after myocardial ischemia/reperfusion) 1.5-fold increased rat survival during the acute post-infarction period in comparison with the control group. In survivors, Di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7afdb73c7839c36916eba41b97c34247
https://doi.org/10.1007/s10517-020-04876-9
https://doi.org/10.1007/s10517-020-04876-9
Autor:
V. N. Belyaev, Ya. I. Yashin, A. Ya. Yashin, Irina V. Fedorova, I. Yu. Chukicheva, A. V. Kutchin, O. V. Shchukina
Publikováno v:
Russian Chemical Bulletin. 68:2325-2330
The results on amperometric determination of antioxidant activity of a large group of iso-bornylphenols are present. The antioxidant activity is dependent on a degree of sterical hindering of hydroxy groups. The obtained data can be used for employin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a691bbc0d002b37c24a6d8ff28af26cf
https://doi.org/10.1007/s11172-019-2706-x
https://doi.org/10.1007/s11172-019-2706-x
Autor:
I. Yu. Chukicheva, Evgeny V. Buravlev, A. V. Kuchin, Irina V. Fedorova, I. A. Dvornikova, Oksana G. Shevchenko
Publikováno v:
Chemistry of Natural Compounds. 55:658-664
New hydroxycinnamic acid derivatives were synthesized by reacting malonic acid and 4-hydroxybenzaldehydes with isobornyl and/or alkyl substituents. The antiradical, antioxidant, and membrane-protective activities were assessed in various in vitro mod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b6dadd63969a5ad73ef5b16aecb76e6
https://doi.org/10.1007/s10600-019-02772-x
https://doi.org/10.1007/s10600-019-02772-x
Autor:
A. V. Kutchin, I. Yu. Chukicheva, Evgeny V. Buravlev, Oksana G. Shevchenko, Irina V. Fedorova, I. A. Dvornikova
Publikováno v:
Russian Chemical Bulletin. 68:1000-1005
A series of new 2-substituted-1H-benzimidazoles was synthesized on the basis of 4-hydroxybenzaldehydes. Their antioxidant properties were evaluated in the in vitro models and compared with those of known analogs. The structural specifi c features of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c1a1d7d6028f2f4484166b42dd805c0
https://doi.org/10.1007/s11172-019-2510-7
https://doi.org/10.1007/s11172-019-2510-7