Zobrazeno 1 - 10
of 173
pro vyhledávání: '"A. A. Khodonov"'
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:
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
Publikováno v:
Тонкие химические технологии, Vol 1, Iss 1, Pp 27-32 (2006)
The opportunity of design of analogue retinal with replacement of trimethylhexenic ring of a molecule on spiropyran moiety is shown. Process of interaction of the synthesized retinal analogues with bacterioopsin from apomembrane Halobacterium salinar
Externí odkaz:
https://doaj.org/article/18193de7b381432e82eeaa4f75d0ee2d
Autor:
Andrey A. Khodonov, Nikolay E. Belikov, Alexey Yu. Lukin, Alexey V. Laptev, Valery A. Barachevsky, Sergey D. Varfolomeev, Olga V. Demina
Publikováno v:
Colorants, Vol 2, Iss 2, Pp 264-404 (2023)
Methods for preparation of 5′-substituted spiropyrans, their chemical properties, and the effects of various factors on the relative stabilities of the spiropyrans and their isomeric merocyanine forms are examined, reviewed, and discussed.
Externí odkaz:
https://doaj.org/article/d2655fe28f624acda8683ab473695514
Akademický článek
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Autor:
Belikov, Nikolay E., Melnikova, Irina A., Demina, Olga V., Petrovskaya, Lada E., Kryukova, Elena A., Dolgikh, Dmitriy A., Kuzmichev, Pavel K., Chupin, Vladimir V., Lukin, Alexey Yu., Shumsky, Alexei N., Chizhov, Igor, Levin, Peter P., Kirpichnikov, Mikhail P., Varfolomeev, Sergei D., Khodonov, Andrey A.
Publikováno v:
In Mendeleev Communications July-August 2018 28(4):406-408
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
Autor:
A. Khodonov, Sergey Varfolomeev, L. Petrovskaya, A. Safinova, A. Lukin, I. Levina, O. Demina, N. Belikov
Publikováno v:
Russian Journal of Biological Physics and Chemisrty. 7:113-122
In this paper, we consider the studies carried out by the authors aimed at developing new hybrid structures and methods for obtaining a family of photochromic labels capable of photocontrolled interaction with inorganic components, as well as the res