Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Roman A. Drokin"'
Autor:
Victor V. Fedotov, Konstantin V. Savateev, Evgeny N. Ulomsky, Roman A. Drokin, Pavel A. Slepukhin, Vladimir L. Rusinov
Publikováno v:
Molbank, Vol 2023, Iss 1, p M1563 (2023)
A sodium salt of 2-(fur-2-yl)-6-nitro-1,2,4-triazolo[1,5-a]pyrimidin-7-one as a close structural analogue of ZM-241385 was obtained. This heterocycle can serve as an effector for A2a adenosine receptors and possesses antiseptic activity. The structur
Externí odkaz:
https://doaj.org/article/72e14f0911a7475bb4bd41944d02e95b
Autor:
Polina N. Mozharovskaia, Alexandra V. Ivoilova, Roman A. Drokin, Alla V. Ivanova, Alisa N. Kozitsina, Vladimir L. Rusinov
Publikováno v:
Chimica Techno Acta, Vol 9, Iss 4 (2022)
The results of this study of the electrochemical transformation of 3-R-4-hydroxy-1,4-dihydro-7-X-1,2,4-triazolo[5,1-c][1,2,4] obtained by voltammetry are presented. It was found that 3-R-4-hydroxy-1,4-dihydro-7-X-1,2,4-triazolo[5,1-c][1,2,4] derivati
Externí odkaz:
https://doaj.org/article/4e73452673e845eb9c3fe721a3d91f4c
Autor:
Roman A. Drokin, Dmitrii V. Tiufiakov, Alexandrina S. Volobueva, Kristina S Lantseva, Egor K. Voinkov, Mariya A Misyurina, Vladimir V. Zarubaev, Evgeny N. Ulomsky, Yana L Esaulkova, Vladimir L. Rusinov, Pavel A. Slepukhin
Publikováno v:
Chemistry of Heterocyclic Compounds
Chem. Heterocycl. Compd.
Chem. Heterocycl. Compd.
[Figure not available: see fulltext.] An azo coupling reaction of α-nitro ketones with 5-diazoazoles was used to obtain 4-alkyl-3-nitro-1,4-dihydroazolo[5,1-с][1,2,4]triazines, which were characterized with respect to their antiviral activity again
Autor:
Alexander A. Spasov, Vladimir L. Rusinov, Egor K. Voinkov, D. D. Shamshina, Roman A. Drokin, M. Yu. Kalenova, E. N. Ulomskiy, R. A. Litvinov, L. E. Usmianova, E. A. Muraveva, P. M. Vasiliev
Publikováno v:
Russian Journal of Bioorganic Chemistry. 46:1278-1284
Protein glycation and the formation of advanced glycation end products (AGEs) play an important role in the pathogenesis of diabetes mellitus (DM) complications, neurodegenerations, and age-related diseases. A model to predict antiglycation activity
Autor:
Roman A. Drokin, Valery N. Charushin, Oleg N. Chupakhin, Egor K. Voinkov, Evgeny N. Ulomsky, Vladimir L. Rusinov
Publikováno v:
Chemistry of Heterocyclic Compounds. 56:1254-1273
The review summarizes and analyzes data from modern information sources on the methods of synthesis of azolo[X,Y-c][1,2,4]triazines. Approaches to the construction of the condensed azolotriazine heterocyclic system are considered and classified, the
Autor:
E. L. Gerasimova, A. V. Ivanova, Roman A. Drokin, Evgeny B. Gorbunov, Vladimir L. Rusinov, E. N. Ulomskiy, E. R. Gazizullina, Marya Borisova
Publikováno v:
Analytical and Bioanalytical Chemistry. 412:5147-5155
The course of viral diseases is accompanied by excessive generation of active oxygen metabolites, so the effectiveness of treatment can be improved by combining antiviral and antioxidant therapy. There was a screening of antioxidant properties of 6-n
Autor:
Egor K. Voinkov, Roman A. Drokin, Victor V. Fedotov, Ilya I. Butorin, Konstantin V. Savateev, Daniil N. Lyapustin, Denis A. Gazizov, Evgeny B. Gorbunov, Pavel A. Slepukhin, Natalya A. Gerasimova, Natalya P. Evstigneeva, Natalya V. Zilberberg, Nikolay V. Kungurov, Evgeny N. Ulomsky, Vladimir L. Rusinov
Publikováno v:
ChemistrySelect. 7
Autor:
Vladimir L. Rusinov, Dmitrii V. Tiufiakov, Egor K. Voinkov, Evgeny N. Ulomsky, Roman A. Drokin
Publikováno v:
Mendeleev Communications. 30:177-179
A new safe synthesis of α-nitro ketone salts via alkaline hydrolysis of 2-morpholino-1-nitroalkenes has been developed. The salts were introduced into the reactions of diazotization and heterocyclization. Crystal structures of new 2-morpholino-1-nit
Autor:
Grigory V. Zyryanov, Dmitry S. Kopchuk, Roman A. Drokin, Ekaterina S. Starnovskaya, Igor A. Khalymbadzha, Eugeny N. Ulomsky, Kousik Giri, Vladimir L. Rusinov, Oleg N. Chupakhin, Yaroslav K. Shtaitz, Alexey P. Krinochkin, Sougata Santra
Publikováno v:
ChemistrySelect. 3:8202-8206
Autor:
Evgeny B. Gorbunov, Oleg N. Chupakhin, Daniil N. Lyapustin, Oleg S. Eltsov, Victor V. Fedotov, Egor K. Voinkov, E. N. Ulomskiy, K. V. Savateev, Roman A. Drokin, Evgeny M. Mukhin, Vladimir L. Rusinov
Publikováno v:
Chemistry of Heterocyclic Compounds. 54:63-69
Nucleophilic substitution of nitro group in 1-alkylazolo[5,1-c][1,2,4]triazin-4(1H)-ones proceeds according to the ANRORC mechanism, involving the opening of azine ring, nucleophilic substitution, and cyclization. The structures of all intermediates