An Insight into the Anti-Cancer Potential of N-Heterocyclic Compounds Targeting Breast Cancer
Abstract: Breast cancer remains one of the leading causes of cancer-related deaths worldwide, so it is crucial to develop novel therapeutic agents to improve treatment outcomes. Nheterocyclic compounds have garnered considerable interest due to their potential in treating breast cancer. N-heterocyclic compounds have been demonstrated to interact with key molecular targets implicated in breast cancer progression, including Estrogen Receptors (ER), HER2, and the PI3K/Akt/mTOR signaling pathway. This review explores the role of N-heterocyclic compounds, including azetidine, imidazole, pyridine, quinoline, and pyrazole, in breast cancer treatment, focusing on their anticancer activity and efficacy. A total of 66 research studies from the PubMed and Google Scholar platforms were cited in the manuscript, demonstrating that N-heterocyclic analogs exhibit superior anticancer activity compared to standard drugs such as doxorubicin and paclitaxel. Different patents related to derivatives and clinical trials reported in the paper confirm the anti-cancer potential of N-heterocyclic compounds. The content of the paper will surely be beneficial to researchers working on the synthesis of novel N-heterocycles and to those seeking to discover more anticancer agents featuring the lead N-heterocyclic moiety. The selection of this sample size ensures comprehensive analytical depth, providing a representative pool for recent studies relevant to the role of N-heterocyclics in Breast Cancer.
Authors
- Shruti Varshney (ORCID: https://orcid.org/0000-0001-9936-8128)
- Rupa Mazumder
- Anjna Rani
- Rakhi Mishra
- Ashish Maurya
- Komal .
- Avijit Mazumder
Institutions
- Jaypee Institute of Information Technology (IN)
Publication Details
- Journal
- Current Organic Chemistry
- Published
- 2026-02-23
- DOI
- https://doi.org/10.2174/0113852728400723251121095338
- Primary Topic
- Synthesis and biological activity
- Type
- article
- Field-Weighted Citation Impact
- 0.00