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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
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 Vasilevsky Sergey F. 1 , Govdi Anastasiya I. 1 , Shults El'vira E. 2 , Shakirov Makhmut M. 2 , Sorokina Irina V. 2 , Tolstikova Tatyana G. 2 , Baev Dmitry S. 2 , Tolstikov Genrikh A. 2 , Alabugin Igor V. 3
Организации
1 (Данные Web of science) Russian Acad Sci, Inst Chem Kinet & Combust, Siberian Branch, Novosibirsk 630090, Russia
2 (Данные Web of science) Russian Acad Sci, NN Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia
3 (Данные Web of science) Florida State Univ, Dept Chem & Biochem, Tallahassee, FL 32306 USA

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 OpenAlex
Даты:
Опубликована в печати: 1 июл. 2009 г.
Идентификаторы БД:
Web of science: WOS:000267873000037
Scopus: 2-s2.0-67650178255
РИНЦ: 13604783
OpenAlex: W2086099335
Цитирование в БД:
БД Цитирований
Web of science 49
Scopus 50
РИНЦ 53
OpenAlex 50
Альметрики: