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Redox conversions of 5-methyl-6-nitro-7-oxo-4,7-dihydro-1,2,4triazolo[1,5-a]pyrimidinide l-arginine monohydrate as a promising antiviral drug. / Ivoilova, Alexandra; Mikhalchenko, Ludmila V.; Tsmokalyuk, Anton et al.
In: Molecules, Vol. 26, No. 16, 5087, 02.08.2021.

Research output: Contribution to journal › Article › peer-review

Harvard

Ivoilova, A, Mikhalchenko, LV, Tsmokalyuk, A, Leonova, M, Lalov, A, Mozharovskaia, P, Kozitsina, AN, Ivanova, AV & Rusinov, VL 2021, 'Redox conversions of 5-methyl-6-nitro-7-oxo-4,7-dihydro-1,2,4triazolo[1,5-a]pyrimidinide l-arginine monohydrate as a promising antiviral drug', Molecules, vol. 26, no. 16, 5087. https://doi.org/10.3390/molecules26165087

APA

Ivoilova, A., Mikhalchenko, L. V., Tsmokalyuk, A., Leonova, M., Lalov, A., Mozharovskaia, P., Kozitsina, A. N., Ivanova, A. V., & Rusinov, V. L. (2021). Redox conversions of 5-methyl-6-nitro-7-oxo-4,7-dihydro-1,2,4triazolo[1,5-a]pyrimidinide l-arginine monohydrate as a promising antiviral drug. Molecules, 26(16), [5087]. https://doi.org/10.3390/molecules26165087

Vancouver

Ivoilova A, Mikhalchenko LV, Tsmokalyuk A, Leonova M, Lalov A, Mozharovskaia P et al. Redox conversions of 5-methyl-6-nitro-7-oxo-4,7-dihydro-1,2,4triazolo[1,5-a]pyrimidinide l-arginine monohydrate as a promising antiviral drug. Molecules. 2021 Aug 2;26(16):5087. doi: 10.3390/molecules26165087

Author

Ivoilova, Alexandra ; Mikhalchenko, Ludmila V. ; Tsmokalyuk, Anton et al. / Redox conversions of 5-methyl-6-nitro-7-oxo-4,7-dihydro-1,2,4triazolo[1,5-a]pyrimidinide l-arginine monohydrate as a promising antiviral drug. In: Molecules. 2021 ; Vol. 26, No. 16.

BibTeX

@article{2a9d8d4b0b8345469fa65ec3baec1277,
title = "Redox conversions of 5-methyl-6-nitro-7-oxo-4,7-dihydro-1,2,4triazolo[1,5-a]pyrimidinide l-arginine monohydrate as a promising antiviral drug",
keywords = "Antiviral drugs, Cyclic voltammetry, ESR spectroscopy, Nitro group transformations, Nitro-1,2,4-triazolo[1,5a]pyrimidines, Nitroaromatic compounds, Nitroheterocyclic compounds, Triazid, 4-triazolo[1, nitroaromatic compounds, STABILITY, nitro group transformations, nitro-1, antiviral drugs, PROTONATION, 2, 5a]pyrimidines, cyclic voltammetry, NITRO-COMPOUNDS, RADICALS, nitroheterocyclic compounds",
author = "Alexandra Ivoilova and Mikhalchenko, {Ludmila V.} and Anton Tsmokalyuk and Marina Leonova and Andrey Lalov and Polina Mozharovskaia and Kozitsina, {Alisa N.} and Ivanova, {Alla V.} and Rusinov, {Vladimir L.}",
note = "Publisher Copyright: {\textcopyright} 2021 by the authors. Licensee MDPI, Basel, Switzerland.",
year = "2021",
month = aug,
day = "2",
doi = "10.3390/molecules26165087",
language = "English",
volume = "26",
journal = "Molecules",
issn = "1420-3049",
publisher = "Multidisciplinary Digital Publishing Institute (MDPI)",
number = "16",

}

RIS

TY - JOUR

T1 - Redox conversions of 5-methyl-6-nitro-7-oxo-4,7-dihydro-1,2,4triazolo[1,5-a]pyrimidinide l-arginine monohydrate as a promising antiviral drug

AU - Ivoilova, Alexandra

AU - Mikhalchenko, Ludmila V.

AU - Tsmokalyuk, Anton

AU - Leonova, Marina

AU - Lalov, Andrey

AU - Mozharovskaia, Polina

AU - Kozitsina, Alisa N.

AU - Ivanova, Alla V.

AU - Rusinov, Vladimir L.

N1 - Publisher Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland.

PY - 2021/8/2

Y1 - 2021/8/2

KW - Antiviral drugs

KW - Cyclic voltammetry

KW - ESR spectroscopy

KW - Nitro group transformations

KW - Nitro-1,2,4-triazolo[1,5a]pyrimidines

KW - Nitroaromatic compounds

KW - Nitroheterocyclic compounds

KW - Triazid

KW - 4-triazolo[1

KW - nitroaromatic compounds

KW - STABILITY

KW - nitro group transformations

KW - nitro-1

KW - antiviral drugs

KW - PROTONATION

KW - 2

KW - 5a]pyrimidines

KW - cyclic voltammetry

KW - NITRO-COMPOUNDS

KW - RADICALS

KW - nitroheterocyclic compounds

UR - http://www.scopus.com/inward/record.url?scp=85113455111&partnerID=8YFLogxK

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000690022300001

UR - https://elibrary.ru/item.asp?id=47010323

U2 - 10.3390/molecules26165087

DO - 10.3390/molecules26165087

M3 - Article

C2 - 34443674

AN - SCOPUS:85113455111

VL - 26

JO - Molecules

JF - Molecules

SN - 1420-3049

IS - 16

M1 - 5087

ER -

ID: 23694014