Zobrazeno 1 - 10
of 153
pro vyhledávání: '"A. V. Kutchin"'
Autor:
Ruba Y. Mahmoud, Elena Y. Trizna, Rand K. Sulaiman, Roman S. Pavelyev, Ilmir R. Gilfanov, Svetlana A. Lisovskaya, Olga V. Ostolopovskaya, Larisa L. Frolova, Alexander V. Kutchin, Galina B. Guseva, Elena V. Antina, Mikhail B. Berezin, Liliya E. Nikitina, Airat R. Kayumov
Publikováno v:
Antibiotics, Vol 11, Iss 12, p 1743 (2022)
Infectious diseases caused by various nosocomial microorganisms affect worldwide both immunocompromised and relatively healthy persons. Bacteria and fungi have different tools to evade antimicrobials, such as hydrolysis damaging the drug, efflux syst
Externí odkaz:
https://doaj.org/article/a916a7a942e74772a72940509c254e47
Autor:
Nikita O. Ilchenko, Denis V. Sudarikov, Roman V. Rumyantcev, Diana R. Baidamshina, Nargiza D. Zakarova, Monyr Nait Yahia, Airat R. Kayumov, Aleksandr V. Kutchin, Svetlana A. Rubtsova
Publikováno v:
Antibiotics, Vol 11, Iss 11, p 1548 (2022)
The widespread presence of multidrug-resistant pathogenic microorganisms challenges the development of novel chemotype antimicrobials, insensitive to microbial tools of resistance. To date, various monoterpenoids have been shown as potential antimicr
Externí odkaz:
https://doaj.org/article/96bf660233ab417490c0412d56e50ab1
Autor:
Polina A. Petrova, Denis V. Sudarikov, Larisa L. Frolova, Roman V. Rumyantcev, Svetlana A. Rubtsova, Aleksandr V. Kutchin
Publikováno v:
Molecules, Vol 27, Iss 20, p 7068 (2022)
For the first time, monoterpene trifluoromethylated β-hydroxy-benzyl-O-oximes were synthesized in 81–95% yields by nucleophilic addition of the Ruppert–Prakash reagent (TMSCF3) to the corresponding β-keto-benzyl-O-oximes based on (+)-nopinone,
Externí odkaz:
https://doaj.org/article/3d6cbd8c14984c6dacd9eeb30be74aa0
Autor:
Ya. A. Gur’eva, O. A. Zalevskaya, N. S. Nikolaeva, Yu. R. Aleksandrova, E. Yu. Yandulova, M. E. Neganova, A. V. Kutchin
Publikováno v:
Russian Chemical Bulletin. 72:793-801
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::464d06c2e27f835b69e7b2963e1e0eba
https://doi.org/10.1007/s11172-023-3843-7
https://doi.org/10.1007/s11172-023-3843-7
Chiral zinc complexes with terpene derivatives of ethylenediamine: synthesis and biological activity
Autor:
Y. A. Gur’eva, O. A. Zalevskaya, N. S. Nikolaeva, Yu. R. Aleksandrova, E. Yu. Yandulova, M. E. Neganova, P. A. Slepukhin, A. V. Kutchin
Publikováno v:
Russian Chemical Bulletin. 71:2612-2620
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0da2f67b70c5e11ec07f6eb675ee669d
https://doi.org/10.1007/s11172-022-3690-0
https://doi.org/10.1007/s11172-022-3690-0
Autor:
Liliya E. Nikitina, Roman S. Pavelyev, Ilmir R. Gilfanov, Sergei V. Kiselev, Zulfiya R. Azizova, Alexander A. Ksenofontov, Pavel S. Bocharov, Elena V. Antina, Vladimir V. Klochkov, Ayzira F. Timerova, Ilfat Z. Rakhmatullin, Olga V. Ostolopovskaya, Mohammed A. Khelkhal, Sergei V. Boichuk, Aigul R. Galembikova, Natalia S. Andriutsa, Larisa L. Frolova, Alexander V. Kutchin, Airat R. Kayumov
Publikováno v:
Bioengineering, Vol 9, Iss 1, p 24 (2022)
Platelet aggregation causes various diseases and therefore challenges the development of novel antiaggregatory drugs. In this study, we report the possible mechanism of platelet aggregation suppression by newly synthesized myrtenol-derived monoterpen
Externí odkaz:
https://doaj.org/article/0f32e3e5cc6e46ee8cc6eefcd99f5219
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
Publikováno v:
Russian Chemical Bulletin. 71:1856-1862
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75757f66ed23b5c1ff89efc1b80d4c37
https://doi.org/10.1007/s11172-022-3602-3
https://doi.org/10.1007/s11172-022-3602-3
Autor:
Svetlana A. Popova, Evgenia V. Pavlova, Oksana G. Shevchenko, Irina Yu. Chukicheva, Aleksandr V. Kutchin
Publikováno v:
Molecules, Vol 26, Iss 12, p 3579 (2021)
The pyrazoline ring is defined as a “privileged structure” in medicinal chemistry. A variety of pharmacological properties of pyrazolines is associated with the nature and position of various substituents, which is especially evident in diarylpyr
Externí odkaz:
https://doaj.org/article/046972aa1b86404eb1a7741e5ee8f79c