Discovery of a Novel G-Quadruplex and Histone Deacetylase (HDAC) Dual-Targeting Agent for the Treatment of Triple-Negative Breast Cancer

التفاصيل البيبلوغرافية
العنوان: Discovery of a Novel G-Quadruplex and Histone Deacetylase (HDAC) Dual-Targeting Agent for the Treatment of Triple-Negative Breast Cancer
المؤلفون: Xin-Chen Jiang, Fang-Hai Tu, Li-Yuan Wei, Bo-Zheng Wang, Hao Yuan, Jing-Mei Yuan, Yong Rao, Shi-Liang Huang, Qing-Jiang Li, Tian-Miao Ou, Hong-Gen Wang, Jia-Heng Tan, Shuo-Bin Chen, Zhi-Shu Huang
المصدر: Journal of Medicinal Chemistry. 65:12346-12366
بيانات النشر: American Chemical Society (ACS), 2022.
سنة النشر: 2022
مصطلحات موضوعية: Histone Deacetylase Inhibitors, Zinc, Cell Line, Tumor, Drug Discovery, Humans, Molecular Medicine, Antineoplastic Agents, Apoptosis, Triple Negative Breast Neoplasms, DNA, Xenograft Model Antitumor Assays, Histone Deacetylases, Cell Proliferation
الوصف: The development of triple-negative breast cancer (TNBC) is highly associated with G-quadruplex (G4); thus, targeting G4 is a potential strategy for TNBC therapy. Because concomitant histone deacetylases (HDAC) inhibition could amplify the impact of G4-targeting compounds, we designed and synthesized two novel series of G4/HDAC dual-targeting compounds by connecting the zinc-binding pharmacophore of HDAC inhibitors to the G4-targeting isaindigotone scaffold (
تدمد: 1520-4804
0022-2623
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69ee936cf4c88cd1bc4652ea3f6093fb
https://doi.org/10.1021/acs.jmedchem.2c01058
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....69ee936cf4c88cd1bc4652ea3f6093fb
قاعدة البيانات: OpenAIRE