Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Anastasia D. Shagina"'
Autor:
Eugene P. Kramarova, Sophia S. Borisevich, Edward M. Khamitov, Alexander A. Korlyukov, Pavel V. Dorovatovskii, Anastasia D. Shagina, Konstantin S. Mineev, Dmitri V. Tarasenko, Roman A. Novikov, Alexey A. Lagunin, Ivan Boldyrev, Aiarpi A. Ezdoglian, Natalia Yu. Karpechenko, Tatiana A. Shmigol, Yuri I. Baukov, Vadim V. Negrebetsky
Publikováno v:
Molecules, Vol 27, Iss 21, p 7542 (2022)
The synthesis of the products of the 1,3-propanesultone ring opening during its interaction with amides of pyridinecarboxylic acids has been carried out. The dependence of the yield of the reaction products on the position (ortho-, meta-, para-) of t
Externí odkaz:
https://doaj.org/article/080c465885b4411f8fc49211e013f536
Autor:
Denis A. Borozdenko, Tatiana A. Shmigol, Aiarpi A. Ezdoglian, Darya I. Gonchar, Natalia. Y. Karpechenko, Dmitri N. Lyakhmun, Anastasia D. Shagina, Elvira A. Cherkashova, Daria D. Namestnikova, Ilya L. Gubskiy, Anastasia A. Chernysheva, Nina M. Kiseleva, Vadim V. Negrebetsky, Yuri I. Baukov
Publikováno v:
Molecules, Vol 27, Iss 17, p 5488 (2022)
Ischemic stroke triggers a whole cascade of pathological changes in the brain, one of which is postischemic inflammation. Since in such cases thrombolytic therapy is often not possible, methods that modulate inflammation and affect microglia become p
Externí odkaz:
https://doaj.org/article/27b819cb2f634fceb1c8be1441e6cfb5
Autor:
Denis A. Borozdenko, Aiarpi A. Ezdoglian, Tatiana A. Shmigol, Darya I. Gonchar, Dmitri N. Lyakhmun, Dmitri V. Tarasenko, Yaroslav V. Golubev, Elvira A. Cherkashova, Daria D. Namestnikova, Ilya L. Gubskiy, Alexey A. Lagunin, Leonid V. Gubsky, Vladimir P. Chekhonin, Sophia S. Borisevich, Maxim A. Gureev, Anastasia D. Shagina, Nina M. Kiseleva, Vadim V. Negrebetsky, Yuri I. Baukov
Publikováno v:
Molecules, Vol 26, Iss 20, p 6124 (2021)
We performed an in silico, in vitro, and in vivo assessment of a potassium 2-[2-(2-oxo-4-phenylpyrrolidin-1-yl) acetamido]ethanesulfonate (compound 1) as a potential prodrug for cognitive function improvement in ischemic brain injury. Using in silico
Externí odkaz:
https://doaj.org/article/2b3a5471b2ee494e851c618e38e99ac8
Autor:
Eugenia P. Kramarova, Alexander D. Volodin, Vadim V. Negrebetsky, Anastasia D. Shagina, Teimur M. Aliev, Pavel V. Dorovatovskii, Roman A. Novikov, Anna V. Vologzhanina, Alexander A. Korlyukov
Publikováno v:
Molecules, Vol 26, Iss 12, p 3548 (2021)
Hexacoordinated heteroligand silicon catecholates, although being prospective as easily soluble compounds with high hydrolytic stability and diverse redox properties, have been insufficiently studied. The transesterification of 1-(trimethoxysilylmeth
Externí odkaz:
https://doaj.org/article/a66c756aeb9f479eac1c7d54eab46f8a
Autor:
Vad. V. Negrebetsky, Anastasia D. Shagina, K. A. Sobyanin, Tatiana A. Shmigol, Evgeniya P. Kramarova, Alexey Lagunin, Yu. I. Baukov, D. N. Lyakhman, D. V. Tarasenko, D. I. Gonchar
Publikováno v:
Russian Chemical Bulletin. 70:479-486
A virtual set of new lactam-containing derivatives of arylsulfonylglycines 1a–d and 2a–d was designed and analyzed using structure–activity computer models (web-services PASS Online, AntiBac-Pred, and GUSAR Acutetoxicity). The antimicrobial act
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1dff890363fb7e6cdd73bb1951cbe4bb
https://doi.org/10.1007/s11172-021-3112-8
https://doi.org/10.1007/s11172-021-3112-8
Autor:
Yu. I. Baukov, Vad. V. Negrebetsky, A. G. Shipov, Anastasia D. Shagina, D. V. Tarasenko, Evgeniya P. Kramarova
Publikováno v:
Russian Chemical Bulletin. 69:398-400
The reaction of N-trimethylsilyl derivatives of amides and imides with alkyl sulfonates on heating affords the corresponding N-alkyl derivatives and trimethylsilyl sulfonates.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d49a055188da38561f3dcf0d2905d77e
https://doi.org/10.1007/s11172-020-2775-x
https://doi.org/10.1007/s11172-020-2775-x
Publikováno v:
Journal of Organometallic Chemistry. 880:29-38
One-pot reaction of FcCH(R)OH with equimolar quantities of BunLi and EtOCOCl followed by an excess of amine produces N-(α-ferrocenylalkyl)amines in up to 98% yields. Nitrogen heteroaryl amines undergo the α-ferrocenylalkylation at the amino group.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8decc1dcb88001a0ba6ff3f39e4d0f54
https://doi.org/10.1016/j.jorganchem.2018.10.021
https://doi.org/10.1016/j.jorganchem.2018.10.021
Autor:
Ekaterina V. Shevaldina, Sergey K. Moiseev, Anastasia D. Shagina, Andrey B. Ponomaryov, Alexandr F. Smol'yakov, Valery N. Kalinin
Publikováno v:
Journal of Organometallic Chemistry. :1-7
α-Ferrocenylalkyl carbonates were demonstrated to be the species for ferrocenylalkylation reactions. The α-ferrocenylalkyl carbonates FcCH(R)OCOOEt (1a-c, Fc = ferrocenyl) were easily generated in situ by a reaction of the α-ferrocenyl substituted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8e7fd8d4270953d07ea0233908a8b16
https://doi.org/10.1016/j.jorganchem.2017.02.044
https://doi.org/10.1016/j.jorganchem.2017.02.044