Design, synthesis and anticancer evaluation of chrysin-1,3,5-triazine derivatives

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. <b>RQ-6</b> 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, <b>RQ-6</b> demonstrates notable <i>in vitro</i> 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 <i>in vivo</i> potential of this compound.

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Publication Details

Journal
Natural Product Research
Published
2026-03-26
DOI
https://doi.org/10.1080/14786419.2026.2647366
Primary Topic
Synthesis and Characterization of Heterocyclic Compounds
Type
article
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article

Design, synthesis and anticancer evaluation of chrysin-1,3,5-triazine derivatives

Rongbin Wei, XuanYi Xue, Cong Qi, Dahua Shi et al.
Natural Product Research
Synthesis and Characterization of Heterocyclic Compounds
article

Design, synthesis and anticancer evaluation of chrysin-1,3,5-triazine derivatives

Rongbin Wei, XuanYi Xue, Cong Qi, Dahua Shi, Luyao Wang, Ming Hu, Yuanfen Zhai, Yamin Ding
article en

Abstract

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. <b>RQ-6</b> 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, <b>RQ-6</b> demonstrates notable <i>in vitro</i> 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 <i>in vivo</i> potential of this compound.

Natural Product Research
Ocean Institute (US), Zhuhai People's Hospital (CN)
Good health and well-being
Openalex Percentile: Top 8%
Synthesis and Characterization of Heterocyclic Compounds
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