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Synthesis and in vitro antifungal activity of selenium-containing chitin derivatives

Anton Romanovich Egorov 1
Anton Romanovich Egorov
Niyaz Zakievich Yagafarov 1, 2
Niyaz Zakievich Yagafarov
Alexey Antonovich Artemjev 1
Alexey Antonovich Artemjev
Omar Muslimovich Khubiev 1
Omar Muslimovich Khubiev
Badreddine Medjbour 1
Badreddine Medjbour
Vladimir Andreevich Kozyrev 1
Vladimir Andreevich Kozyrev
Nkumbu Donovan Sikaona 1
Nkumbu Donovan Sikaona
Olga I Tsvetkova 1
Olga I Tsvetkova
Vasili V Rubanik 3
Vasili V Rubanik
Vasili V.,Jr. Rubanik 3
Vasili V.,Jr. Rubanik
Aleh V Kurliuk 4
Aleh V Kurliuk
Tatsiana Vladimirovna Shakola 4
Tatsiana Vladimirovna Shakola
Ilya Sergeyevich Kritchenkov 1, 3, 5
Ilya Sergeyevich Kritchenkov
Alexander G Tskhovrebov 1
Alexander G Tskhovrebov
Analoly Aleksandrovich Kirichuk 1
Analoly Aleksandrovich Kirichuk
Victor Nikolaevich Khrustalev
Andreii Sergeevich Kritchenkov 1, 3
Andreii Sergeevich Kritchenkov
Published 2022-04-29
CommunicationVolume 32, Issue 3, 357-359
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Egorov A. R. et al. Synthesis and in vitro antifungal activity of selenium-containing chitin derivatives // Mendeleev Communications. 2022. Vol. 32. No. 3. pp. 357-359.
GOST all authors (up to 50) Copy
Egorov A. R., Yagafarov N. Z., Artemjev A. A., Khubiev O. M., Medjbour B., Kozyrev V. A., Sikaona N. D., Tsvetkova O. I., Rubanik V. V., Rubanik V. V., Kurliuk A. V., Shakola T. V., Lobanov N. N., Kritchenkov I. S., Tskhovrebov A. G., Kirichuk A. A., Khrustalev V. N., Kritchenkov A. S. Synthesis and in vitro antifungal activity of selenium-containing chitin derivatives // Mendeleev Communications. 2022. Vol. 32. No. 3. pp. 357-359.
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TY - JOUR
DO - 10.1016/j.mencom.2022.05.022
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2022.05.022
TI - Synthesis and in vitro antifungal activity of selenium-containing chitin derivatives
T2 - Mendeleev Communications
AU - Egorov, Anton Romanovich
AU - Yagafarov, Niyaz Zakievich
AU - Artemjev, Alexey Antonovich
AU - Khubiev, Omar Muslimovich
AU - Medjbour, Badreddine
AU - Kozyrev, Vladimir Andreevich
AU - Sikaona, Nkumbu Donovan
AU - Tsvetkova, Olga I
AU - Rubanik, Vasili V
AU - Rubanik, Vasili V.,Jr.
AU - Kurliuk, Aleh V
AU - Shakola, Tatsiana Vladimirovna
AU - Lobanov, Nikolai Nikolaevich
AU - Kritchenkov, Ilya Sergeyevich
AU - Tskhovrebov, Alexander G
AU - Kirichuk, Analoly Aleksandrovich
AU - Khrustalev, Victor Nikolaevich
AU - Kritchenkov, Andreii Sergeevich
PY - 2022
DA - 2022/04/29
PB - Mendeleev Communications
SP - 357-359
IS - 3
VL - 32
ER -
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@article{2022_Egorov,
author = {Anton Romanovich Egorov and Niyaz Zakievich Yagafarov and Alexey Antonovich Artemjev and Omar Muslimovich Khubiev and Badreddine Medjbour and Vladimir Andreevich Kozyrev and Nkumbu Donovan Sikaona and Olga I Tsvetkova and Vasili V Rubanik and Vasili V.,Jr. Rubanik and Aleh V Kurliuk and Tatsiana Vladimirovna Shakola and Nikolai Nikolaevich Lobanov and Ilya Sergeyevich Kritchenkov and Alexander G Tskhovrebov and Analoly Aleksandrovich Kirichuk and Victor Nikolaevich Khrustalev and Andreii Sergeevich Kritchenkov},
title = {Synthesis and in vitro antifungal activity of selenium-containing chitin derivatives},
journal = {Mendeleev Communications},
year = {2022},
volume = {32},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2022.05.022},
number = {3},
pages = {357--359},
doi = {10.1016/j.mencom.2022.05.022}
}
MLA
Cite this
MLA Copy
Egorov, Anton Romanovich, et al. “Synthesis and in vitro antifungal activity of selenium-containing chitin derivatives.” Mendeleev Communications, vol. 32, no. 3, Apr. 2022, pp. 357-359. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2022.05.022.

Keywords

[1,2,4]selenadiazolo[4,5-a]pyridin-4-ium salts
alkylation
Antifungal activity
chitin
organoselenium compounds
ultrasound

Abstract

Mild and ‘green’ ultrasound-assisted reaction of chitin with 3-(chloromethyl)[1,2,4]selenadiazolo[4,5-a]pyridin-4-ium bromide in water affords novel selenium-containing cationic chitin derivatives. The thus obtained chitin derivatives are water soluble and are characterized by high in vitro antifungal activity comparable with conventional antifungal drug Amphotericin B.

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