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Synthesis of (1S)-(+)-camphor-10-sulfonic acid derivatives and investigations in vitro and in silico of their antiviral activity as the inhibitors of fi lovirus infections Научная публикация

Журнал Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171
Вых. Данные Год: 2019, Том: 68, Номер: 5, Страницы: 1041-1046 Страниц : 6 DOI: 10.1007/s11172-019-2517-0
Ключевые слова Marburg virus; Ebola virus; pseudotyped viruses; (1S)-(+)-camphor-10-sulfonic acid; N-heterocycles; molecular docking
Авторы Sokolova A.S. 1 , Baranova D.V. 1,2 , Yarovaya O.I. 1,2 , Baev D.S. 1,2 , Polezhaeva O.A. 3 , Zybkina A.V. 3 , Shcherbakov D.N. 3 , Tolstikova T.G. 1,2 , Salakhutdinov N.F. 1,2
Организации
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, 9 Prosp Akad Lavrenteva, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, 2 Ul Pirogova, Novosibirsk 630090, Russia
3 (Данные Web of science) State Res Ctr Virol & Biotechnol Vector, Koltsov 630559, Novosibirsk Reg, Russia

Реферат: N-Heterocycle-containing (1S)-(+)-camphor-10-sulfonamide derivatives were synthesized. Their antiviral activity against the Ebola and Marburg viruses was estimated using a pseudovirus system based on the vesicular stomatitis virus. The derivatives bearing morpholine and triazole moieties demonstrated the highest inhibitory activity towards the Ebola virus glycoprotein. A moderate activity against the Marburg virus was found for a compound containing the piperidine moiety. A molecular modeling of the interaction between the synthesized derivatives and the binding site of glycoprotein of the Ebola virus was performed.
Библиографическая ссылка: Sokolova A.S. , Baranova D.V. , Yarovaya O.I. , Baev D.S. , Polezhaeva O.A. , Zybkina A.V. , Shcherbakov D.N. , Tolstikova T.G. , Salakhutdinov N.F.
Synthesis of (1S)-(+)-camphor-10-sulfonic acid derivatives and investigations in vitro and in silico of their antiviral activity as the inhibitors of fi lovirus infections
Russian Chemical Bulletin. 2019. V.68. N5. P.1041-1046. DOI: 10.1007/s11172-019-2517-0 WOS Scopus РИНЦ OpenAlex
Оригинальная: Соколова А.С. , Баранова Д.В. , Яровая О.И. , Баев Д.С. , Полежаева О.А. , Зыбкина А.В. , Щербаков Д.Н. , Толстикова Т.Г. , Салахутдинов Н.Ф.
Синтез производных (1s)-(+)-камфора-10-сульфокислоты и изучение их противовирусной активности в качестве ингибиторов филовирусных инфекций in vitro и in silico
Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2019. №5. С.1041-1046. РИНЦ
Даты:
Опубликована в печати: 1 мая 2019 г.
Опубликована online: 11 июн. 2019 г.
Идентификаторы БД:
Web of science: WOS:000471201700015
Scopus: 2-s2.0-85067183336
РИНЦ: 41633816
OpenAlex: W2949180311
Цитирование в БД:
БД Цитирований
Web of science 19
Scopus 21
РИНЦ 29
OpenAlex 24
Альметрики: