Реферат: Conjugates of isatin and hydrazones based on (+)-camphor and (–)-fenchone were synthesized for the first time. The physicochemical properties of the synthesized compounds have been studied, and for the hydrazone product of fenchone and isatin X-ray diffraction data have been obtained. Molecular modeling of the possible interaction of new compounds with the active site of the basic protease 3CLpro of the SARS-CoV-2 virus was carried out, and the properties of isatin-terpene compounds as inhibitors of the 3CLpro protease were studied. It was found that the new conjugates do not exhibit inhibitory properties against 3CLpro, which makes it possible to clarify the direction of further chemical modifications of monoterpenoid derivatives in order to obtain molecules with antiviral properties.

Библиографическая ссылка: Yarovaya O.I. , Baev D.S. , Kovaleva K.S. , Gatilov Y.V. , Meshkova Y.V. , Marinina M.K. , Oreshko V.V. , Tolstikova T.G. , Salakhutdinov N.F.
Synthesis and Properties of New Conjugates of Isatin and Bicyclic Monoterpenes
Russian Journal of General Chemistry. 2024. V.94. N1. P.81-92. DOI: 10.1134/s1070363224010080 WOS Scopus OpenAlex

Даты:

Поступила в редакцию:	6 дек. 2023 г.
Принята к публикации:	7 дек. 2023 г.
Опубликована в печати:	16 апр. 2024 г.

Идентификаторы БД:

Web of science:	WOS:001203968700002
Scopus:	2-s2.0-85190501423
OpenAlex:	W4394836921

Цитирование в БД: Пока нет цитирований

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