Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Nikolai A. Aksenov"'
Autor:
Arif Idris Ismiev, Gunay Zakhid Mamedova, Victor V. Dotsenko, Nikolai A. Aksenov, Inna V. Aksenova, Abel Mamedali Magerramov
Publikováno v:
Proceedings, Vol 9, Iss 1, p 1 (2019)
oxobicyclo[3.2.1]octane-2,4-dicarboxylates. The structures of the products were confirmed by NMR and X-ray analysis.
Externí odkaz:
https://doaj.org/article/818c990818d7481aa9ffa9ff8973180a
Autor:
Daria Kriger, Ksenia Novitskaya, Giomar Vasileva, Ekaterina Lomert, Nikolai D. Aksenov, Nikolai A. Barlev, Dmitri Tentler
Publikováno v:
Biology Direct, Vol 17, Iss 1, Pp 1-13 (2022)
Abstract Background ACTN4 is an actin-binding protein involved in many cellular processes, including cancer development. High ACTN4 expression is often associated with a poor prognosis. However, it has been identified as a positive marker for platinu
Externí odkaz:
https://doaj.org/article/3a43fef6c46d498db97f0104f51fa5f6
Autor:
Igor Yu. Grishin, Vladimir V. Malyuga, Dmitrii А. Aksenov, Nikita K. Kirilov, Gasan M. Abakarov, Sergei N. Ovcharov, Andrei V. Sarapii, Nikolai А. Aksenov, Alexander V. Aksenov
Publikováno v:
Chemistry of Heterocyclic Compounds. 58:313-318
Autor:
Nikolai A. Aksenov, Victor V. Dotsenko, Gennady D. Krapivin, Vladimir K. Vasilin, Tatyana A. Stroganova
Publikováno v:
Tetrahedron Letters. 60:997-1000
The oxidation of 3-aminothieno[2,3-b]pyridine-2-carboxamides with commercially available bleach leads to the formation of dimeric pyrrolo[2′,3′:4,5]thieno[2,3-b]pyridines (7a,14a-diamino-7,14-bis(aryl)-7,7a,14,14a-tetrahydro-6H,13H-pyrido[3″″
Autor:
A. D. Pugachev, I. A. Rostovtseva, A. S. Kozlenko, Nikolai A. Aksenov, Valery V. Tkachev, Nadezhda I. Makarova, Maria B. Lukyanova, I. V. Ozhogin, Boris S. Lukyanov
Publikováno v:
Journal of Molecular Structure. 1178:590-598
New indoline spiropyrans containing conjugated cationic fragments and bulky substituents in the 2H-chromene moiety were synthesized by a simple one-pot method. The structures of the obtained compounds were confirmed by 1H and 13C NMR (including 2D me
Publikováno v:
Chemistry of Heterocyclic Compounds. 54:964-970
A number of 2,6-diazido-4-methylnicotinonitrile derivatives has been synthesized as prospective novel plant growth regulators. The 2-[(triphenylphosphoranylidene)amino]tetrazolo[1,5-a]pyridine derivative is selectively formed from 2,6-diazido-4-methy
Autor:
Alexey Petukhov, Alena Kizenko, Aigul Shakirova, Nickolai A. Barlev, Alexandra Daks, Oleg Shuvalov, Olga A. Fedorova, Elena A. Vasileva, Nikolai D. Aksenov
Publikováno v:
Biochemical and Biophysical Research Communications. 495:1233-1239
As an anticancer therapeutic, Interferon-alpha (IFNα) is used to treat a number of malignancies. However, the application of IFNα is restricted mostly due to its high toxicity. Therefore, novel combination therapeutic regimens are required to decre
Autor:
Stanislav Herashchenko, Igor E. Garkusha, V.V. Chebotarev, Valery Valentynovych Staltsov, Nikolai V Kulik, Vadym A Makhlai, M.S. Ladygina, S. Pestchanyi, Yurij Petrov, Nikolai N Aksenov, O.V. Byrka
Publikováno v:
Nuclear Fusion. 61:116040
This paper presents experimental studies of plasma-surface interactions during powerful plasma impacts of a Quasi-Stationary Plasma Accelerator (QSPA) on the Sn capillary porous systems (CPSs) in conditions, simulating disruption and Edge Localized M
Autor:
Nikolai A. Barlev, Alexey Petukhov, Nikolai V Panyushev, Kirill V. Volkov, Alina D. Nikotina, Nikolai D. Aksenov, Mittenberg Ag, Daria Kriger, M.G. Khotin, Dmitri Tentler, Turoverova Lv, Ekaterina Lomert
Publikováno v:
Cell Cycle. :01-21
Alpha-actinin 4 (ACTN4) is an actin-binding protein of the spectrin superfamily. ACTN4 is found both in the cytoplasm and nucleus of eukaryotic cells. The main function of cytoplasmic ACTN4 is stabilization of actin filaments and their binding to foc
Autor:
Inna V. Aksenova, K. A. Frolov, Victor V. Dotsenko, Sergey G. Krivokolysko, A. N. Khrustaleva, Nikolai A. Aksenov
Publikováno v:
Chemistry of Heterocyclic Compounds. 53:887-891
The aminomethylation reaction of 9-benzyl-2,4-dioxo-3,9-diazaspiro[5.5]undecane-1,5-dicarbonitrile hydrochloride in the presence of primary aliphatic amines and an excess of 37% aqueous formaldehyde led to the formation of 7-substituted 1'-benzyl-2,4