Efficient synthesis of the first betulonic acid-acetylene hybrids and their hepatoprotective and anti-inflammatory activity Научная публикация
Журнал |
Bioorganic and Medicinal Chemistry
ISSN: 0968-0896 , E-ISSN: 1464-3391 |
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Вых. Данные | Год: 2009, Том: 17, Номер: 14, Страницы: 5164-5169 Страниц : DOI: 10.1016/j.bmc.2009.05.059 | ||||||
Ключевые слова | Cross-coupling; Arylacetylenes; Betulonic acid; Triterpenoids; Hepatoprotection; Anti-inflammatory activity | ||||||
Авторы |
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Организации |
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Реферат:
The Sonogashira reaction can be applied for the preparation of acetylenic derivatives of betulonic acid where the triterpenoid moiety can serve as either the halo- or the acetylenic component. This reaction opened access to the first derivatives of betulonic acid containing either the arylethynyl (C equivalent to C-Ar(Het) or the ethynyl (C equivalent to CH) moieties. From the fundamental perspective, this work illustrates the possibility of selective Pd-catalyzed cross-coupling at terminal acetylenes in the presence of a terminal alkene. Hepatoprotective and anti-inflammatory properties of selected acetylenic derivatives of betulonic acid were investigated using the CCl4-induced hepatitis and carrageenan-induced edema models, respectively. (C) 2009 Elsevier Ltd. All rights reserved.
Библиографическая ссылка:
Vasilevsky S.F.
, Govdi A.I.
, Shults E.E.
, Shakirov M.M.
, Sorokina I.V.
, Tolstikova T.G.
, Baev D.S.
, Tolstikov G.A.
, Alabugin I.V.
Efficient synthesis of the first betulonic acid-acetylene hybrids and their hepatoprotective and anti-inflammatory activity
Bioorganic and Medicinal Chemistry. 2009. V.17. N14. P.5164-5169. DOI: 10.1016/j.bmc.2009.05.059 WOS Scopus РИНЦ
Efficient synthesis of the first betulonic acid-acetylene hybrids and their hepatoprotective and anti-inflammatory activity
Bioorganic and Medicinal Chemistry. 2009. V.17. N14. P.5164-5169. DOI: 10.1016/j.bmc.2009.05.059 WOS Scopus РИНЦ
Даты:
Опубликована в печати: | 1 июл. 2009 г. |
Идентификаторы:
Web of science | WOS:000267873000037 |
Scopus | 2-s2.0-67650178255 |
РИНЦ | 13604783 |
OpenAlex | W2086099335 |