14β-(Isoxazol-3-yl)methylestrane Steroids: Chemoselective Synthesis and Transformations with Heterocyclic Ring Opening
- Авторы: Baranovsky A.V.1, Ladyko A.S.1, Shatskaya V.A.2, Scherbakov A.M.2
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Учреждения:
- Institute of Bioorganic Chemistry
- Blokhin National Medical Research Center of Oncology
- Выпуск: Том 55, № 2 (2019)
- Страницы: 202-214
- Раздел: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/219862
- DOI: https://doi.org/10.1134/S107042801902012X
- ID: 219862
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Аннотация
Steroids containing an isoxazole, isoxazoline, or enaminocarbonyl substituent at C-14 and a C-14-C-15-fused pyrrolidine ring were synthesized. The influence of solvents on the result of dipolar cycloaddition and solvolysis of bridged nitrosteroids was evaluated. Cytotoxicity testing of estrone analogs on cancer cells of various origins revealed activity against breast, colorectal, prostate, and lung cancer cells.
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Об авторах
A. Baranovsky
Institute of Bioorganic Chemistry
Автор, ответственный за переписку.
Email: baranovsky@iboch.by
Белоруссия, ul. Kuprevicha 5/2, Minsk, 220147
A. Ladyko
Institute of Bioorganic Chemistry
Email: alex.scherbakov@gmail.com
Белоруссия, ul. Kuprevicha 5/2, Minsk, 220147
V. Shatskaya
Blokhin National Medical Research Center of Oncology
Email: alex.scherbakov@gmail.com
Россия, Kashirskoe shosse 24, Moscow, 115522
A. Scherbakov
Blokhin National Medical Research Center of Oncology
Автор, ответственный за переписку.
Email: alex.scherbakov@gmail.com
Россия, Kashirskoe shosse 24, Moscow, 115522
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