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Synthesis and antiviral properties of tricyclic amides derived from α-humulene and β-caryophyllene Научная публикация

Журнал Mendeleev Communications
ISSN: 0959-9436
Вых. Данные Год: 2022, Том: 32, Номер: 5, Страницы: 609-611 Страниц : 3 DOI: 10.1016/j.mencom.2022.09.013
Авторы Yarovaya Olga I. 1 , Kovaleva Kseniya S. 1 , Borisevich Sophia S. 2 , Rybalova Tatyana V. 1 , Gatilov Yuriy V. 1 , Sinegubova Ekaterina O. 3 , Volobueva Alexandrina S. 3 , Zarubaev Vladimir V. 3 , Salakhutdinov Nariman F. 1
Организации
1 N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry of Siberian Branch of Russian Academy of Sciences
2 Ufa Institute of Chemistry, RAS
3 Saint Petersburg Pasteur Institute

Реферат: The Ritter reaction of humulene with acetonitrile occurs as the biomimetic process to afford the amide having the skeleton of a natural alcohol. The structures of the amides obtained from humulene and caryophyllene were confirmed by XRD data. The activity of some cage compounds against influenza virus allowed one to suggest the mechanism of antiviral action based on interfering with membrane fusion activity of viral hemagglutinin.
Библиографическая ссылка: Yarovaya O.I. , Kovaleva K.S. , Borisevich S.S. , Rybalova T.V. , Gatilov Y.V. , Sinegubova E.O. , Volobueva A.S. , Zarubaev V.V. , Salakhutdinov N.F.
Synthesis and antiviral properties of tricyclic amides derived from α-humulene and β-caryophyllene
Mendeleev Communications. 2022. V.32. N5. P.609-611. DOI: 10.1016/j.mencom.2022.09.013 WOS Scopus РИНЦ OpenAlex
Идентификаторы БД:
Web of science: WOS:000874166100013
Scopus: 2-s2.0-85139328869
РИНЦ: 53959982
OpenAlex: W4302759495
Цитирование в БД:
БД Цитирований
OpenAlex 5
Web of science 2
РИНЦ 3
Альметрики: