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Synthesis and biological activity of novel deoxycholic acid derivatives Научная публикация

Журнал Bioorganic and Medicinal Chemistry
ISSN: 0968-0896 , E-ISSN: 1464-3391
Вых. Данные Год: 2015, Том: 23, Номер: 15, Страницы: 5022-5034 Страниц : DOI: 10.1016/j.bmc.2015.05.012
Ключевые слова Bile acids; Deoxycholic acid derivatives; Cytotoxicity; Nitric oxide; Biological activity
Авторы Popadyuk Irina I. 1 , Markov Andrey V. 2 , Salomatina Oksana V. 1 , Logashenko Evgeniya B. 2 , Shernyukov Andrey V. 1 , Zenkova Marina A. 2 , Salakhutdinov Nariman F. 1,3
Организации
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia
2 (Данные Web of science) Russian Acad Sci, Siberian Branch, Inst Chem Biol & Fundamental Med, Novosibirsk 630090, Russia
3 (Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia

Реферат: We report the synthesis and biological activity of new semi-synthetic derivatives of naturally occurring deoxycholic acid (DCA) bearing 2-cyano-3-oxo-1-ene, 3-oxo-1(2)-ene or 3-oxo-4(5)-ene moieties in ring A and 12-oxo or 12-oxo-9(11)-ene moieties in ring C. Bioassays using murine macrophage-like cells and tumour cells show that the presence of the 9(11)-double bond associated with the increased polarity of ring A or with isoxazole ring joined to ring A, improves the ability of the compounds to inhibit cancer cell growth. (C) 2015 Elsevier Ltd. All rights reserved.
Библиографическая ссылка: Popadyuk I.I. , Markov A.V. , Salomatina O.V. , Logashenko E.B. , Shernyukov A.V. , Zenkova M.A. , Salakhutdinov N.F.
Synthesis and biological activity of novel deoxycholic acid derivatives
Bioorganic and Medicinal Chemistry. 2015. V.23. N15. P.5022-5034. DOI: 10.1016/j.bmc.2015.05.012 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 авг. 2015 г.
Идентификаторы БД:
Web of science: WOS:000358440000093
Scopus: 2-s2.0-84937513123
РИНЦ: 23991725
OpenAlex: W2236053983
Цитирование в БД:
БД Цитирований
Web of science 21
Scopus 20
РИНЦ 18
OpenAlex 22
Альметрики: