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Updated: Mar 27, 2026

Functionalized Spirocyclic Heterocycle Synthesis and Cytotoxicity Assay
Published on: February 9, 2021
Design, synthesis and anticancer evaluation of chrysin-1,3,5-triazine derivatives
Rongbin Wei1,2, Cong Qi1, Xuanyi Xue1
1Jiangsu Key Laboratory of Marine Pharmaceutical Compound Screening, College of Pharmacy, Jiangsu Ocean University, Lianyungang, China.
None:
Breast cancer is the most frequently diagnosed malignancy in women and a primary contributor to cancer-related mortality worldwide. Despite significant advances in treatment, a substantial number of patients with metastatic breast cancer remain unresponsive to treatment. Accordingly, we prepared multiple chrysin-based triazine compounds to assess their anti-proliferative activity against human malignancies, particularly targeting breast cancer cell apoptosis and the related molecular pathways. RQ-6 demonstrated potent inhibition of breast cancer cell proliferation, colony formation, migration, adhesion, and invasion, and induced apoptosis. Additionally, RQ-6 modulated the levels of apoptosis-related proteins and transcriptomically suggested the activation of pathways such as caspase-3, p53, and TNF. In conclusion, RQ-6 demonstrates notable in vitro antineoplastic efficacy in breast cancer cell lines and shows promise as a candidate for further investigation as a therapeutic intervention in breast cancer. Future studies are warranted to confirm the selectivity and in vivo potential of this compound.
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