Zobrazeno 1 - 10
of 99
pro vyhledávání: '"O. V. Demina"'
Autor:
N. E. Belikov, L. E. Petrovskaya, E. A. Kryukova, D. A. Dolgikh, E. P. Lukashev, A. Yu. Lukin, O. V. Demina, S. D. Varfolomeev, V. V. Chupin, A. A. Khodonov
Publikováno v:
Russian Journal of Bioorganic Chemistry. 48:1190-1201
Abstract— We have developed an alternative method for the synthesis of an analog of natural retinal, which contains the p-fluorophenyl fragment instead of the trimethylcyclohexene ring. The proposed scheme for the synthesis of the target all-E-isom
Publikováno v:
Тонкие химические технологии, Vol 9, Iss 1, Pp 18-21 (2014)
The goal of the present study was the development of composition analysis method for vision pigments chromophore groups of different animals with the use of high performance liquid chromatography as well as the development of synthetic method for all
Externí odkaz:
https://doaj.org/article/63a9c69d4d004a8794857b72a44ac03a
Autor:
A. V. Laptev, A. Yu. Lukin, N. V. Belikov, O. V. Demina, S. D. Varfolomeev, V. A. Barachevsky, A. A. Khodonov, V. I. Shvets
Publikováno v:
Тонкие химические технологии, Vol 8, Iss 4, Pp 18-26 (2013)
Few 5-vinyl substituted 6’-nitro-1,3,3-trimethylspiro(indolino-2,2’-[2H]chromenes) (6’-nitro-spiropyrans) were synthesized by a one-step method from 5-formyl precursor – 5-formyl-6’-nitro-1,3,3-trimethylspiro(indolino-2,2’- [2H]chromene)
Externí odkaz:
https://doaj.org/article/641d81e72a5d4b7f90aede13ad8c102d
Autor:
O. V. Demina
Publikováno v:
Geography and Natural Resources. 41:76-82
The state and the prospects of implementation of major investment projects combined into the Eastern Gas Program have been analyzed. The terms of realization, the state of resources and the state of gas transportation system under the projects formin
Autor:
A. A. Khodonov, A. V. Laptev, A. Yu. Lukin, N. E. Belikov, M. A. Fomin, O. V. Demina, D. A. Skladnev, S. A. Tyurin, V. I. Shvets
Publikováno v:
Тонкие химические технологии, Vol 6, Iss 2, Pp 15-36 (2011)
This mini-review presents experimental data obtained by the authors in the context of a cycle of structural-functional research on bionanophotochrome bacteriorhodopsin carried out during the past 10 years. We reviewed the synthetic routes and structu
Externí odkaz:
https://doaj.org/article/0a1dab24c82d4f6cbd4b3de30c490153
Synthesis of new 3,5-substiuted isoxazole derivatives possessing potential anti-aggregative activity
Autor:
O. V. Demina, A. V. Laptev, A. U. Lukin, N. E. Belikov, K. V. Zvezdin, M. A. Fomin, A. A. Khodonov, S. D. Varfolomeev, V. I. Shvets
Publikováno v:
Тонкие химические технологии, Vol 5, Iss 6, Pp 47-51 (2010)
Two new compounds belonging to 3,5-substituted isoxazoles class were synthesized for the action mechanism investigation and the pharmacophore fragment determination of potential anti-aggregative compounds of this class. An attempt to prepare of 5-phe
Externí odkaz:
https://doaj.org/article/417b5c8a205f424a97370109f1be6a3a
Autor:
A. Yu. Lukin, Irina Melnikova, A. A. Khodonov, Sergey D. Varfolomeev, O. V. Demina, N. E. Belikov
Publikováno v:
Russian Journal of Physical Chemistry B. 13:938-941
Guidelines and principles for the development of new labels and probes for bionanophotonics, methods for their preparation, and labeling procedures for various targets are briefly discussed.
Publikováno v:
Problems of Uninterrupted Medical Training and Science. 2017:66-69
Autor:
Sergei D. Varfolomeev, Pavel Kuzmichev, N. E. Belikov, E. A. Kryukova, D. A. Dolgikh, Vladimir Chupin, Peter P. Levin, Lada E. Petrovskaya, A. A. Khodonov, Alexei N. Shumsky, Alexey Lukin, Irina Melnikova, Mikhail P. Kirpichnikov, Igor Chizhov, O. V. Demina
Publikováno v:
Mendeleev Communications. 28:406-408
The effects of chromophoric group structures on the functional properties of bacteriorhodopsin (BR) and proteorhodopsin from E. sibiricum (ESRh) were compared. ESRh retinal binding site was found as preserving the similar stereo- and spatial restrict
Publikováno v:
Russian Chemical Bulletin. 63:2092-2113
A series of 5-substituted 3-pyridylisoxazoles were synthesized using [3+2] cycloaddition of nitrile oxides to alkynes with variation of substituents at position 5 of the isoxazole ring without additional synthetic stages and with retention of 2-pyrid