Search Results - "Matyugina, E. S."

Cytotoxicity Studies of 5-Arylaminouracil Derivatives by Kezin, V. A., Matyugina, E. S., Surzhikov, S. A., Novikov, M. S., Maslova, A. A., Karpenko, I. L., Ivanov, A. V., Kochetkov, S. N., Khandazhinskaya, A. L.

“…We have previously shown that 5-arylaminouracil derivatives can inhibit HIV-1, herpesviruses, mycobacteria, and other pathogens through various mechanisms. The…”
Get full text

Evaluation of the Antiviral Potential of Modified Heterocyclic Base and 5'-Norcarbocyclic Nucleoside Analogs Against SARS-CoV-2 by Matyugina, E S, Novikov, M S, Kozlovskaya, L I, Volok, V P, Shustova, E Y, Ishmukhametov, A A, Kochetkov, S N, Khandazhinskaya, A L

“…The pandemic caused by the novel betacoronavirus SARS-CoV-2 has already claimed more than 3.5 million lives. Despite the development and use of anti-COVID-19…”
Get full text

5′-Norcarbocyclic nucleoside analogs by Matyugina, E. S., Khandazhinskaya, A. L.

“…The present review briefly outlines main methods for the synthesis of 5′-norcarbocyclic nucleoside analogs and the biological activity spectrum of these…”
Get full text

5-Arylaminouracil Derivatives as Potential Dual-Action Agents by Matyugina, E S, Novikov, M S, Babkov, D A, Valuev-Elliston, V T, Vanpouille, C, Zicari, S, Corona, A, Tramontano, E, Margolis, L B, Khandazhinskaya, A L, Kochetkov, S N

“…Several 5-aminouracil derivatives that have previously been shown to inhibit Mycobacterium tuberculosis growth at concentrations of 5-40 μg/mL are demonstrated…”
Get full text

Carbocyclic analogues of inosine-5'-monophosphate: synthesis and biological activity by Matyugina, E S, Andreevskaya, S N, Smirnova, T G, Khandazhinskaya, A L

“…9-(4'-Phosphonomethoxy-2'-cyclopenten-1'-yl)hypoxanthine and 9-(4'-phosphonomethoxy-2',3'-dihydroxycyclopenten-1'-yl)hypoxanthine were synthesized as isosteric…”
Get full text

Synthesis and antiviral evaluation against the Vaccinia virus of new N ₁-oxide analogs of 5′-noraristeromycin by Matyugina, E. S, Seley-Radtke, K. L, Andronova, V. L, Galegov, G. A, Kochetkov, S. N, Khandazhinskaya, A. L

“…New N ₁-benzyl esters of N ₁-oxide analogues of 5′-noraristeromycin were synthesized and tested as potential inhibitors of S-adenosyl-L-homocysteine hydrolase…”
Get full text

Synthesis and antiviral evaluation against the Vaccinia virus of new N1-oxide analogs of 5′-noraristeromycin by Matyugina, E. S., Seley-Radtke, K. L., Andronova, V. L., Galegov, G. A., Kochetkov, S. N., Khandazhinskaya, A. L.

“…New N 1 -benzyl esters of N 1 -oxide analogues of 5′-noraristeromycin were synthesized and tested as potential inhibitors of S -adenosyl- L -homocysteine…”
Get full text

Aryl-Containing Esters Of Triphosphoric Acid As Substrates Of Terminal Deoxynucleotidyl Transferase by Khandazhinskaya, A. L., Matyugina, E. S., Alexandrova, L. A., Shirokova, E. A., Kukhanova, M. K., Jasko, M. V.

“…A new group of terminal deoxynucleotidyltransferase (TDT) substrates, namely, non-nucleoside triphosphates (NNTP) bearing 5-substituted 2,4-dinitrophenyl…”
Get full text

Structure-functional analysis of interactions of terminal deoxynucleotidyl transferase with new non-nucleoside substrates by Matyugina, E S, Alexandrova, L A, Jas'ko, M V, Ivanov, A V, Vasil'ev, I A, Lapteva, V L, Khandazhinskaya, A L, Kukhanova, M K

“…New non-nucleoside esters of phosphoric acid containing various hydrophobic groups, namely (1) N-(2-tripticencarbonyl)-4-aminobutyl; (2) 5-phenylsubstituted…”
Get more information

Cytotoxicity Studies of 5-Arylaminouracil Derivatives by Kezin, V A, Matyugina, E S, Surzhikov, S A, Novikov, M S, Maslova, A A, Karpenko, I L, Ivanov, A V, Kochetkov, S N, Khandazhinskaya, A L

“…We have previously shown that 5-arylaminouracil derivatives can inhibit HIV-1, herpesviruses, mycobacteria, and other pathogens through various mechanisms. The…”
Get more information

Structure-functional analysis of interactions of terminal deoxynucleotidyl transferase with new non-nucleoside substrates by Matyugina, E. S., Alexandrova, L. A., Jasco, M. V., Ivanov, A. V., Vasiliev, I. A., Lapteva, V. L., Khandazhinskaya, A. L., Kukhanova, M. K.

“…New non-nucleoside esters of phosphoric acid containing various hydrophobic groups, namely (1) N -(2-tripticencarbonyl)-4-aminobutyl; (2) 5-phenylsubstituted N…”
Get full text