Literature DB >> 34763082

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

Jizhao Xie1, Huanji Xu2, Xinduo Wu2, Yunfeng Xie2, Xiuhong Lu3, Lisheng Wang4.   

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.
Copyright © 2021. Published by Elsevier Ltd.

Entities:  

Keywords:  Azeliragon; RAGE inhibitor; SUM149; Triazole analogue; Triple-negative breast cancer

Mesh:

Substances:

Year:  2021        PMID: 34763082     DOI: 10.1016/j.bmcl.2021.128444

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

Review 1.  Advanced Glycation End Products and Diabetes Mellitus: Mechanisms and Perspectives.

Authors:  Mariyam Khalid; Georg Petroianu; Abdu Adem
Journal:  Biomolecules       Date:  2022-04-04

Review 2.  Therapeutic potential of targeting the receptor for advanced glycation end products (RAGE) by small molecule inhibitors.

Authors:  Harbinder Singh; Devendra K Agrawal
Journal:  Drug Dev Res       Date:  2022-07-04       Impact factor: 5.004

  2 in total

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