Synthesis of camphecene derivatives using click chemistry methodology and study of their antiviral activity Научная публикация
Журнал |
Bioorganic and Medicinal Chemistry Letters
ISSN: 0960-894X , E-ISSN: 1464-3405 |
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Вых. Данные | Год: 2017, Том: 27, Номер: 10, Страницы: 2181-2184 Страниц : 4 DOI: 10.1016/j.bmcl.2017.03.051 | ||||||||
Ключевые слова | Acetylenes; Antivirals; Azides; Camphor; Click chemistry; Imine derivatives; Influenza; Triazoles | ||||||||
Авторы |
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Организации |
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Реферат:
A series of seventeen tetrazole derivatives of 1,7,7-trimethyl-[2.2.1]bicycloheptane were synthesized using click chemistry methodology and characterized by spectral data. Studies of cytotoxicity and in vitro antiviral activity against influenza virus A/Puerto Rico/8/34 (H1N1) in MDCK cells of the compounds obtained were performed. The structure-activity relationship analysis suggests that to possess virus-inhibiting activity, the compounds of this group should bear oxygen atom with a short linker (C2-C4), either as a hydroxyl group (18, 19, 29), keto-group (21) or as a part of a heterocycle (24). These compounds demonstrated low cytotoxicity along with high anti-viral activity. (C) 2017 Published by Elsevier Ltd.
Библиографическая ссылка:
Artyushin O.I.
, Sharova E.V.
, Vinogradova N.M.
, Genkina G.K.
, Moiseeva A.A.
, Klemenkova Z.S.
, Orshanskaya I.R.
, Shtro A.A.
, Kadyrova R.A.
, Zarubaev V.V.
, Yarovaya O.I.
, Salakhutdinov N.F.
, Brel V.K.
Synthesis of camphecene derivatives using click chemistry methodology and study of their antiviral activity
Bioorganic and Medicinal Chemistry Letters. 2017. V.27. N10. P.2181-2184. DOI: 10.1016/j.bmcl.2017.03.051 WOS Scopus РИНЦ
Synthesis of camphecene derivatives using click chemistry methodology and study of their antiviral activity
Bioorganic and Medicinal Chemistry Letters. 2017. V.27. N10. P.2181-2184. DOI: 10.1016/j.bmcl.2017.03.051 WOS Scopus РИНЦ
Даты:
Опубликована в печати: | 1 мая 2017 г. |
Идентификаторы:
Web of science | WOS:000401492500021 |
Scopus | 2-s2.0-85016578082 |
РИНЦ | 29482366 |
OpenAlex | W2598861224 |