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Mechanism of the 2-ethyl-3-hydroxy-6-methylpyridinium 2-nitroxysuccinate reduction in nitrite-generating systems

Olesya Viktorovna Pokidova 1
Olesya Viktorovna Pokidova
Boris L'vovich Psikha 1
Boris L'vovich Psikha
Alexander Ivanovich Kotelnikov 1, 2
Alexander Ivanovich Kotelnikov
Boris Sergeevich Fedorov 1
Boris Sergeevich Fedorov
Published 2020-06-26
CommunicationVolume 30, Issue 4, 482-484
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Pokidova O. V. et al. Mechanism of the 2-ethyl-3-hydroxy-6-methylpyridinium 2-nitroxysuccinate reduction in nitrite-generating systems // Mendeleev Communications. 2020. Vol. 30. No. 4. pp. 482-484.
GOST all authors (up to 50) Copy
Pokidova O. V., Psikha B. L., Kormukhina A. Y., Kotelnikov A. I., Fedorov B. S. Mechanism of the 2-ethyl-3-hydroxy-6-methylpyridinium 2-nitroxysuccinate reduction in nitrite-generating systems // Mendeleev Communications. 2020. Vol. 30. No. 4. pp. 482-484.
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TY - JOUR
DO - 10.1016/j.mencom.2020.07.025
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2020.07.025
TI - Mechanism of the 2-ethyl-3-hydroxy-6-methylpyridinium 2-nitroxysuccinate reduction in nitrite-generating systems
T2 - Mendeleev Communications
AU - Pokidova, Olesya Viktorovna
AU - Psikha, Boris L'vovich
AU - Kormukhina, Alexandra Yur'evna
AU - Kotelnikov, Alexander Ivanovich
AU - Fedorov, Boris Sergeevich
PY - 2020
DA - 2020/06/26
PB - Mendeleev Communications
SP - 482-484
IS - 4
VL - 30
ER -
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@article{2020_Pokidova,
author = {Olesya Viktorovna Pokidova and Boris L'vovich Psikha and Alexandra Yur'evna Kormukhina and Alexander Ivanovich Kotelnikov and Boris Sergeevich Fedorov},
title = {Mechanism of the 2-ethyl-3-hydroxy-6-methylpyridinium 2-nitroxysuccinate reduction in nitrite-generating systems},
journal = {Mendeleev Communications},
year = {2020},
volume = {30},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2020.07.025},
number = {4},
pages = {482--484},
doi = {10.1016/j.mencom.2020.07.025}
}
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Pokidova, Olesya Viktorovna, et al. “Mechanism of the 2-ethyl-3-hydroxy-6-methylpyridinium 2-nitroxysuccinate reduction in nitrite-generating systems.” Mendeleev Communications, vol. 30, no. 4, Jun. 2020, pp. 482-484. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2020.07.025.

Keywords

cysteine
Griess method
nitrite ion
organic nitrate
thionitrate

Abstract

The nitrite-generating activity of 2-ethyl-3-hydroxy-6-methylpyridinium 2-nitroxysuccinate as a promising NO-donor has been investigated in reactions with various reducing agents. Reduction of the NO-donor with cysteine was analyzed using a kinetic modeling method. The calculated rate constants satisfactorily describe the experimental data, thereby confirming the proposed reaction mechanism.

References

1.
10.1016/j.mencom.2020.07.025_bib0005
Nitric Oxide: Biology and Pathobiology, 2000
2.
10.1016/j.mencom.2020.07.025_bib0010
Nitric Oxide Donors for Pharmaceutical and Biological Applications, 2005
3.
l-Arginine and nitric oxide synthesis in the cells with inducible NO synthase
Kuropteva Z.V., Baider L.M., Nagler L.G., Bogatyrenko T.N., Belaia O.L.
Russian Chemical Bulletin, 2019
4.
B. S. Fedorov, M.A. Fadeev, V.N. Varfolomeev, M.I. Retskij, G.N. Bliznetsova and E. V. Neborak, RU Patent 2394815 C2, 2010.
5.
Antioxidant Properties of a Pharmaceutical Substance Hypocard, a Potential Drug for Ischemic Disease
Neganova M.E., Klochkov S.G., Shevtsova E.F., Bogatyrenko T.N., Mishchenko D.V.
Bulletin of Experimental Biology and Medicine, 2018
6.
The Reactivity of 3-Hydroxy-6-methyl-2-ethylpyridine 2-Nitroxysuccinate and Reference Drugs in Model NO-Generating Systems
Pokidova O.V., Batova E.V., Sadkov A.P., Eremeev A.B., Fedorov B.S., Kotelnikov A.I.
Doklady Chemistry, 2019
7.
Effect of Mexidol and Nitroxymexidol on Phosphodiesterase Activity, Some Oxidation Processes, and Hypoxia Resistance
Tat’yanenko L.V., Dobrokhotova O.V., Varfolomeev V.N., Fadeev M.A., Fedorov B.S., Shtol’ko V.N., Mishchenko D.V.
Pharmaceutical Chemistry Journal, 2014
12.
Modeling of the Bioactivation of an Organic Nitrate by a Thiol to Form a Thionitrate Intermediate
14.
NO problem for nitroglycerin: organic nitrate chemistry and therapy
15.
The emerging biology of the nitrite anion
Gladwin M.T., Schechter A.N., Kim-Shapiro D.B., Patel R.P., Hogg N., Shiva S., Cannon R.O., Kelm M., Wink D.A., Espey M.G., Oldfield E.H., Pluta R.M., Freeman B.A., Lancaster J.R., Feelisch M., et. al.
Nature Chemical Biology, 2005
17.
10.1016/j.mencom.2020.07.025_bib0085
Granik
Oksid azota (NO). Novyi put’ k poisku lekarstv [Nitric Oxide (NO). A New Way to Drug Search], 2004
18.
10.1016/j.mencom.2020.07.025_bib0090
Musil
Biochemistry in Schematic Perspective, Avicenum, 1980