Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Viktor G. Kartsev"'
Autor:
Alina D. Nikotina, Snezhana A. Vladimirova, Nadezhda E. Kokoreva, Elena Y. Komarova, Nikolay D. Aksenov, Sergey Efremov, Elizaveta Leonova, Rostislav Pavlov, Viktor G. Kartsev, Zhichao Zhang, Boris A. Margulis, Irina V. Guzhova
Publikováno v:
Pharmaceuticals, Vol 15, Iss 8, p 923 (2022)
Despite significant progress in the diagnosis and treatment of colorectal cancer, drug resistance continues to be a major limitation of therapy. In this regard, studies aimed at creating combination therapy are gaining popularity. One of the most pro
Externí odkaz:
https://doaj.org/article/95091978f5174c428b61b1cc9fcb38c8
Autor:
SAMVEL N. SIRAKANYAN, ATHINA GERONIKAKI, DOMENICO SPINELLI, ELMIRA K. HAKOBYAN, VIKTOR G. KARTSEV, ANTHI PETROU, ANUSH A. HOVAKIMYAN
Publikováno v:
Anais da Academia Brasileira de Ciências, Iss 0 (2018)
ABSTRACT Annulated thienopyrimidine derivatives attracted big interest of the scientific community due to their broad spectrum of biological activities among which are the inhibition of phosphodiesterase, antiproliferative and antimicrobial activitie
Externí odkaz:
https://doaj.org/article/e378532b994a4a4c9d73dbb6aeb2e0d7
Autor:
Gennadii S. Borodkin, Alexander I. Klimenko, L.N. Fetisov, Vadim S. Sochnev, Lyudmila N. Divaeva, Anatolii S. Morkovnik, Alexander A. Zubenko, Anatolii N. Bodryakov, Oleg P. Demidov, Viktor G. Kartsev, Marya A. Bodryakova, Natalia Dobaeva
Publikováno v:
Mendeleev Communications. 31:125-127
1-Chloromethyl-3,4-dihydroisoquinolines upon treatment with thioureas under acidic conditions undergo recyclization to afford new β-[o-(thiazol-4-yl)aryl]ethylamines.
Autor:
Viktor G Kartsev, Sergey G. Polonik, Elena Y. Komarova, Boris A. Margulis, Elizaveta Leonova, Dmitry G. Alexeev, Alina D. Nikotina, Sergey M. Efremov, Snezhana A Vladimirova, Irina V. Guzhova, Rostislav V. Pavlov
Publikováno v:
International Journal of Molecular Sciences; Volume 22; Issue 13; Pages: 6902
International Journal of Molecular Sciences, Vol 22, Iss 6902, p 6902 (2021)
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 6902, p 6902 (2021)
International Journal of Molecular Sciences
Hyperglycemia may contribute to the progression of carcinomas by triggering epithelial-to-mesenchymal transition (EMT). Some proteostasis systems are involved in metastasis; in this paper, we sought to explore the mechanism of Hsp70 chaperone in EMT.
Autor:
Viktor G. Kartsev, Phaedra Eleftheriou, Anthi Petrou, Giovanni Maga, R. Boga, B. Bartolo, Athina Geronikaki, G. Franco, E. Crespan
Publikováno v:
SAR and QSAR in Environmental Research. 30:697-714
Nonnucleoside reverse transcriptase inhibitors (NNRTIs) remain the most promising anti-AIDS agents that target the HIV-1 reverse transcriptase enzyme (RT). However, the efficiency of approved NNRTI drugs has decreased by the appearance of drug-resist
Autor:
Samvel N. Sirakanyan, Elmira K. Hakobyan, Athina Geronikaki, Anush A. Hovakimyan, Domenico Spinelli, Viktor G. Kartsev
Publikováno v:
Synthetic Communications. 49:1262-1276
Taking into account previously obtained biological results on some polyheterocyclic compounds (containing different heteroatoms) and in particular on several 8-amino-5-isopropyl-2,2-dimethyl-10-(methylthio)-1,4-dihydro-2H-pyrano[4’’,3’’:4’,
Autor:
Viktor G. Kartsev, Samvel N. Sirakanyan, Anush A. Hovakimyan, Domenico Spinelli, Athina Geronikaki, Elmira K. Hakobyan
Publikováno v:
ChemistrySelect. 3:10938-10942
Autor:
E. K. Kultyshkina, Konstantin A. Krasnov, Pavel V. Dorovatovskii, E. V. Dobrokhotova, Viktor G. Kartsev, Ya. V. Zubavichus, Victor N. Khrustalev, N. Yu. Chernikova
Publikováno v:
Chemistry of Natural Compounds. 54:739-744
New heterocyclic quinolizidine systems were prepared from (1R,5S,12S)-tetrahydrocytisine. The synthetic scheme included arylation of tetrahydrocytisine by 2-fluoro-5-nitrobenzaldehyde and condensation of the resulting aldehyde with 1,3-dimethylbarbit
Autor:
Anatolii S. Morkovnik, Alexander A. Zubenko, Kirill Yu. Suponitsky, Viktor G. Kartsev, Lyudmila N. Divaeva, Alexander I. Klimenko
Publikováno v:
Mendeleev Communications. 28:320-322
Derivatives of phenanthro[1,2-d]azepine, a previously unknown heterocyclic system, can be easily obtained from aporphine alkaloids by successive pyridine–pyridine and pyridine–azepine recyclizations. The starting glaucine was used as an illustrat
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.