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A new strategy for the design of macrocycles containing tetrahydrofuran pharmacophores with anticancer activity Научная публикация

Журнал Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Вых. Данные Год: 2026, Том: 75, Номер: 2, Страницы: 533-540 Страниц : 8 DOI: 10.1007/s11172-026-4905-6
Авторы D’yakonov V.A. 1 , Dzhemileva L.U. 1 , Islamov I.I. 2 , Makarova E.Kh. 2 , Gaisin I.V. 2 , Makarov A.A. 2 , Dzhemilev U.M. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation
2 Institute of Petrochemistry and Catalysis, Ufa Federal Research Center, Russian Academy of Sciences, 141 prosp. Oktyabrya, 450075, Ufa, Russian Federation

Реферат: A previously unreported macrodiolide featuring a (Z,Z)-1,5-diene moiety was synthesized stereoselectively by Cp2TiCl2-catalyzed homocyclomagnesiation of functionally substituted 1,2-dienes. Subsequent Ru-catalyzed oxidative cyclization of 1,5-diene bonds within the macrocycle enabled the first synthesis of macrocyclic lactones incorporating 2,5-disubstituted tetrahydrofuran moieties as a pharmacophore. The anticancer activity of the obtained macrocyclic compounds was evaluated against Jurkat, A549, and HEK293 cell lines. The mechanism of action is proposed to be mediated by the ionophore effect of these compounds.
Библиографическая ссылка: D’yakonov V.A. , Dzhemileva L.U. , Islamov I.I. , Makarova E.K. , Gaisin I.V. , Makarov A.A. , Dzhemilev U.M.
A new strategy for the design of macrocycles containing tetrahydrofuran pharmacophores with anticancer activity
Russian Chemical Bulletin. 2026. V.75. N2. P.533-540. DOI: 10.1007/s11172-026-4905-6 WOS Scopus OpenAlex
Даты:
Поступила в редакцию: 25 апр. 2025 г.
Опубликована online: 11 апр. 2026 г.
Идентификаторы БД:
≡ Web of science: WOS:001738024100021
≡ Scopus: 2-s2.0-105035548647
≡ OpenAlex: W7153614926
Альметрики: