14β-(Isoxazol-3-yl)methylestrane Steroids: Chemoselective Synthesis and Transformations with Heterocyclic Ring Opening
- 作者: Baranovsky A.V.1, Ladyko A.S.1, Shatskaya V.A.2, Scherbakov A.M.2
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隶属关系:
- Institute of Bioorganic Chemistry
- Blokhin National Medical Research Center of Oncology
- 期: 卷 55, 编号 2 (2019)
- 页面: 202-214
- 栏目: Article
- URL: https://journals.rcsi.science/1070-4280/article/view/219862
- DOI: https://doi.org/10.1134/S107042801902012X
- ID: 219862
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详细
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.
作者简介
A. Baranovsky
Institute of Bioorganic Chemistry
编辑信件的主要联系方式.
Email: baranovsky@iboch.by
白俄罗斯, ul. Kuprevicha 5/2, Minsk, 220147
A. Ladyko
Institute of Bioorganic Chemistry
Email: alex.scherbakov@gmail.com
白俄罗斯, ul. Kuprevicha 5/2, Minsk, 220147
V. Shatskaya
Blokhin National Medical Research Center of Oncology
Email: alex.scherbakov@gmail.com
俄罗斯联邦, Kashirskoe shosse 24, Moscow, 115522
A. Scherbakov
Blokhin National Medical Research Center of Oncology
编辑信件的主要联系方式.
Email: alex.scherbakov@gmail.com
俄罗斯联邦, Kashirskoe shosse 24, Moscow, 115522
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