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Design, synthesis and anti-TNBC activity of Azeliragon triazole analogues

Authors :
Huanji Xu
Xinduo Wu
Xiuhong Lu
Lisheng Wang
Ji-Zhao Xie
Yunfeng Xie
Source :
Bioorganic & Medicinal Chemistry Letters. 54:128444
Publication Year :
2021
Publisher :
Elsevier BV, 2021.

Abstract

Triple-negative breast cancer (TNBC) is the most aggressive subtype of breast cancer. Many studies have shown a significant increase in the marker signal of the receptor for advanced glycation end-products (RAGE) with the malignant progression of tumor growth, metastasis and recurrence of breast cancer, including TNBC of primary tumors and lymph node metastases. Azeliragon is a RAGE inhibitor and it has been shown to actively inhibit the TNBC cell line, SUM149 (IC50 = 5.292 ± 0.310 μM). In order to develop a new anti-TNBC agent, we designed, synthesized and screened 26 Azeliragon triazole analogues to determine their anti-TNBC activities in vitro. The most active compound was KC-10 with an IC50 value of 0.220 ± 0.034 μM.

Details

ISSN :
0960894X
Volume :
54
Database :
OpenAIRE
Journal :
Bioorganic & Medicinal Chemistry Letters
Accession number :
edsair.doi.dedup.....9162f0cf61198c0d9a28801cfb6d8be1
Full Text :
https://doi.org/10.1016/j.bmcl.2021.128444