Zobrazeno 1 - 10
of 47
pro vyhledávání: '"L. N. Divaeva"'
Autor:
V. V. Zarubaev, S. V. Vasilieva, Y. L. Esaulkova, A. V. Garshinina, V. M. Veprintseva, A. V. Galochkina, Y. S. Protsak, I. V. Teselkin, A. S. Morkovnik, L. N. Divaeva, I. N. Lavrentieva
Publikováno v:
Инфекция и иммунитет, Vol 8, Iss 2, Pp 195-200 (2018)
Influenza is an acute respiratory viral infection, which represents an important health problem. Every year, influenza causes epidemics and pandemics, leading to increase in morbidity and mortality in all regions of the globe. Due to the segmental or
Externí odkaz:
https://doaj.org/article/937dc81199dd4829af7c81afc3581a49
Autor:
A. S. Burlov, L. N. Divaeva, V. G. Vlasenko, Yu. V. V. Koshchienko, B. V. Chaltsev, S. A. Mashchenko, M. A. Kiskin
Publikováno v:
Journal of Structural Chemistry. 63:1284-1290
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5ddc9c739a168684f9be4d136748e38
https://doi.org/10.1134/s0022476622080091
https://doi.org/10.1134/s0022476622080091
Autor:
D. V. Mal’tsev, A. S. Taran, A.S. Morkovnik, M. V. Miroshnikov, L. N. Divaeva, Tat’yana A. Kuz’menko, Alexander A. Spasov, E.A. Zolotova
Publikováno v:
Journal of Volgograd State Medical University. 15:19-23
The article describes the study of anxiolytic activity of a new series of diazepinobenzimidazole derivatives having in their structure two preferential substructures - diazepine and benzimidazole. According to the results of the study a new series of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7906f41ed7e471f235b434e783dcadd5
https://doi.org/10.19163/1994-9480-2018-3(67)-19-23
https://doi.org/10.19163/1994-9480-2018-3(67)-19-23
Autor:
Alexander I. Klimenko, Anatolii S. Morkovnik, Gennadii S. Borodkin, Alexander A. Zubenko, L. N. Divaeva, Victor G. Kartsev
Publikováno v:
Mendeleev Communications. 29:116-118
A simple method for pyridoxal structural modification via furan ring closure was developed resulting in 2-acyl- and 2-heteroarylfuro[2,3-c]pyridines. The reaction products can be proposed as pyridoxal mimetics to inhibit pyridoxal 5′-phosphate-depe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bad26e24a47fd56b2ba7fa501d90453
https://doi.org/10.1016/j.mencom.2019.01.040
https://doi.org/10.1016/j.mencom.2019.01.040
Autor:
Alexander I. Klimenko, Kyrill Yu. Suponitsky, Anatolii S. Morkovnik, V. G. Kartsev, Alexander A. Zubenko, L. N. Divaeva, Gennadii S. Borodkin, Danil V. Alexeenko
Publikováno v:
Tetrahedron Letters. 58:1233-1236
A novel one-pot synthetic route to the poorly studied 4-heteroaryl-1,2-dihydro-3-benzazepine motif from 3,4-dihydroisoquinolinium compounds is described. The synthetic approach is based on heterocyclic ring expansion of isoquinoline substrates upon r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b369d99ccb17aef63704cbfcea00422
https://doi.org/10.1016/j.tetlet.2017.02.036
https://doi.org/10.1016/j.tetlet.2017.02.036
Autor:
Ludmila G. Kuz'mina, Alexander A. Zubenko, L. N. Divaeva, Gennadii S. Borodkin, Anatolii S. Morkovnik, Viktor G. Kartsev, Alexander I. Klimenko
Publikováno v:
Mendeleev Communications. 28:58-60
Using glaucine as an example, a convenient access to naphtho[2,1-f]isoquinoline (litebamine) derivatives is proposed. The synthetic scheme involves a stepwise pyridine–pyridine recyclization of the intermediate N-acylsecoaporphine analogues.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c9141fe69a7bbfa425ddd33e86f658a
https://doi.org/10.1016/j.mencom.2018.01.019
https://doi.org/10.1016/j.mencom.2018.01.019
Autor:
L. N. Divaeva, Viktor G. Kartsev, Alexander I. Klimenko, Gennadii S. Borodkin, Alexander A. Zubenko, Anatolii S. Morkovnik
Publikováno v:
Mendeleev Communications. 28:83-85
2-Methyl-3,4-dihydro-β-carbolin-2-ium iodide in the reaction with aryl halomethyl ketones is converted into 4- or/and 5-acyl-1,2-dihydroazepino[4,5-b]indoles depending on the electron donating effect of substituents in the aryl moiety of the halomet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd050b7338fc8855b849f26c592a2cf5
https://doi.org/10.1016/j.mencom.2018.01.028
https://doi.org/10.1016/j.mencom.2018.01.028
Autor:
L. N. Divaeva, Viktor G. Kartsev, Kyrill Yu. Suponitsky, Alexander A. Zubenko, Anatolii S. Morkovnik
Publikováno v:
ChemistrySelect. 1:2560-2564
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0ffd0b8e3e6021ade800c708542288f
https://doi.org/10.1002/slct.201600727
https://doi.org/10.1002/slct.201600727
Autor:
A F, Kucheryavenko, V A, Anisimova, K A, Gaidukova, L N, Divaeva, T A, Kuz'menko, A S, Morkovnik, V S, Sirotenko, A A, Spasov
Publikováno v:
Eksperimental'naia i klinicheskaia farmakologiia. 79(5)
The antiaggregant activity of a new benzimidazole derivative - 2,3,4,5-tetrahydro[1,3]diazepino[1,2-α]benzimidazole (DAB-15) has been investigated in vitro in comparison to reference drugs acetylsalicylic acid (ASA) and ticlid (ticlopidine) on the m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9b63e1ebfb4aeeca3db62922086bc451
https://pubmed.ncbi.nlm.nih.gov/29782777
https://pubmed.ncbi.nlm.nih.gov/29782777
Publikováno v:
Tetrahedron Letters. 56:6988-6993
A new, one-pot approach to 4-acyl-1,2-dihydro-3-benzazepines has been proposed proceeding via a six- to seven-membered heterocyclic ring expansion under the action of α-haloketones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6387638227ad5650adef779a26f8b2e9
https://doi.org/10.1016/j.tetlet.2015.10.103
https://doi.org/10.1016/j.tetlet.2015.10.103