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Design, synthesis and anti-TNBC activity of Azeliragon triazole analogues
- 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.
- Subjects :
- Glycation End Products, Advanced
Clinical Biochemistry
Pharmaceutical Science
Antineoplastic Agents
Triple Negative Breast Neoplasms
Biochemistry
Metastasis
RAGE (receptor)
Structure-Activity Relationship
Breast cancer
Glycation
Cell Line, Tumor
Drug Discovery
medicine
Humans
Receptor
Molecular Biology
Lymph node
Triple-negative breast cancer
Cell Proliferation
Dose-Response Relationship, Drug
Molecular Structure
Chemistry
Organic Chemistry
Imidazoles
Triazoles
medicine.disease
In vitro
medicine.anatomical_structure
Drug Design
Cancer research
Molecular Medicine
Drug Screening Assays, Antitumor
Subjects
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