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Borneol Ester Derivatives as Entry Inhibitors of aWide Spectrum of SARS-CoV-2 Viruses Научная публикация

Журнал Viruses
ISSN: 1999-4915
Вых. Данные Год: 2022, Том: 14, Номер: 1295, Номер статьи : 1295, Страниц : DOI: 10.3390/v14061295
Ключевые слова SARS-CoV-2; coronavirus surface protein S-spike; pseudoviral system; terpene; borneol; molecular dynamics; molecular docking
Авторы Yarovaya Olga I. 1 , Shcherbakov Dmitriy N. 2 , Borisevich Sophia S. 3 , Sokolova Anastasiya S. 1 , Gureev Maxim A. 4,5 , Khamitov Edward M. 3 , Rudometova Nadezda B. 2 , Zybkina Anastasiya V. 2 , Mordvinova Ekaterina D. 1,2 , Zaykovskaya Anna V. 2 , Rogachev Artem D. 1 , Pyankov Oleg V. 2 , Maksyutov Rinat A. 2 , Salakhutdinov Nariman F. 1
Организации
1 N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry of Siberian Branch of Russian Academy of Sciences
2 State Research Center of Virology and Biotechnology VECTOR
3 Ufa Institute of Chemistry, RAS
4 Sechenov First Moscow State Medical University
5 Sirius University of Science and Technology, Sochi, 354349, Russian Federation

Реферат: In the present work we studied the antiviral activity of the home library of monoterpenoid derivatives using the pseudoviral systems of our development, which have glycoproteins of the SARS-CoV-2 virus strains Wuhan and Delta on their surface. We found that borneol derivatives with a tertiary nitrogen atom can exhibit activity at the early stages of viral replication. In order to search for potential binding sites of ligands with glycoprotein, we carried out additional biological tests to study the inhibition of the re-receptor-binding domain of protein S. For the compounds that showed activity on the pseudoviral system, a study using three strains of the infectious SARS-CoV-2 virus was carried out. As a result, two leader compounds were found that showed activity on the Wuhan, Delta, and Omicron strains. Based on the biological results, we searched for the potential binding site of the leader compounds using molecular dynamics and molecular docking methods. We suggested that the compounds can bind in conserved regions of the central helices and/or heptad repeats of glycoprotein S of SARS-CoV-2 viruses.
Библиографическая ссылка: Yarovaya O.I. , Shcherbakov D.N. , Borisevich S.S. , Sokolova A.S. , Gureev M.A. , Khamitov E.M. , Rudometova N.B. , Zybkina A.V. , Mordvinova E.D. , Zaykovskaya A.V. , Rogachev A.D. , Pyankov O.V. , Maksyutov R.A. , Salakhutdinov N.F.
Borneol Ester Derivatives as Entry Inhibitors of aWide Spectrum of SARS-CoV-2 Viruses
Viruses. 2022. V.14. N1295. 1295 . DOI: 10.3390/v14061295 WOS Scopus РИНЦ OpenAlex
Даты:
Поступила в редакцию: 17 апр. 2022 г.
Принята к публикации: 10 июн. 2022 г.
Опубликована online: 14 июн. 2022 г.
Идентификаторы БД:
Web of science: WOS:000816661400001
Scopus: 2-s2.0-85132563097
РИНЦ: 49151052
OpenAlex: W4282921295
Цитирование в БД:
БД Цитирований
OpenAlex 26
Web of science 22
Альметрики: