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Mendeleev Communications, 2022, Volume 32, Issue 5, Pages 609–611
DOI: https://doi.org/10.1016/j.mencom.2022.09.013 (Mi mendc741) 		 
This article is cited in 5 scientific papers (total in 5 papers)

Communications

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

O. I. Yarovayaa, K. S. Kovalevaa, S. S. Borisevichb, T. V. Rybalovaa, Yu. V. Gatilova, E. O. Sinegubovac, A. S. Volobuevac, V. V. Zarubaevc, N. F. Salakhutdinova

a N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
b Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russian Federation
c St. Petersburg Pasteur Institute, St. Petersburg, Russian Federation
Full-text PDF (607 kB) Citations (5)
DOI: https://doi.org/10.1016/j.mencom.2022.09.013
Abstract: 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.
Keywords: humulene, caryophyllene, acetonitrile, Ritter reaction, amides, antiviral agents, influenza, molecular modeling.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (902.7 Kb)


Citation: O. I. Yarovaya, K. S. Kovaleva, S. S. Borisevich, T. V. Rybalova, Yu. V. Gatilov, E. O. Sinegubova, A. S. Volobueva, V. V. Zarubaev, N. F. Salakhutdinov, “Synthesis and antiviral properties of tricyclic amides derived from α-humulene and β-caryophyllene”, Mendeleev Commun., 32:5 (2022), 609–611
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  • https://www.mathnet.ru/eng/mendc/v32/i5/p609
    • This publication is cited in the following 5 articles:
    1. O. A. Zhupikova, O. I. Yarovaya, M. K. Marenina, Yu. V. Meshkova, S. V. Belenkaya, D. N. Shcherbakov, A. V. Zaykovskaya, O. V. Pyankov, V. V. Zarubaev, M. G. Mikhalsky, A. Yu. Fedorov, S. G. Arkhipov, V. I. Potkin, I. A. Kolesnik, A. V. Ivanov, N. F. Salakhutdinov, M. V. Khvostov, Mendeleev Commun., 35:2 (2025), 145–147  mathnet  crossref
    2. Akram Hegazy, Sara H. Mahmoud, Ahmed Magdy Khalil, Luis Martinez-Sobrido, Ahmed Mostafa, Microbial Genomics: Clinical, Pharmaceutical, and Industrial Applications, 2024, 219  crossref
    3. Fu-Min Zhang, Meng-En Chen, Zhang-Yan Gan, Reference Module in Chemistry, Molecular Sciences and Chemical Engineering, 2024  crossref
    4. Dmitry E. Shybanov, Maxim E. Kukushkin, Yuri K. Grishin, Vitaly A. Roznyatovsky, Viktor A. Tafeenko, Louay Abo Qoura, Vadim S. Pokrovsky, Olga I. Yarovaya, Svetlana V. Belyaevskaya, Alexandrina S. Volobueva, Iana L. Esaulkova, Vladimir V. Zarubaev, Elena K. Beloglazkina, “1,3-Dipolar Cycloaddition of Nitrile Oxides and Nitrilimines to (-)-β-Caryophyllene: Stereoselective Synthesis of Polycyclic Derivatives and Their Biological Testing”, IJMS, 25:21 (2024), 11435  crossref
    5. O. I. Yarovaya, S. S. Laev, N. F. Salakhutdinov, “Antiviral properties of diterpenes and their derivatives”, Russian Chem. Reviews, 92:1 (2023), RCR5056  mathnet  mathnet  crossref  isi  scopus
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