Development of novel pyrimidine-thio-triazoles targeting EGFR in breast Cancer cells via one-pot copper-catalyzed 1,3-dipolar cycloaddition

IF 2.5 Q2 CHEMISTRY, MULTIDISCIPLINARY

Results in Chemistry Pub Date : 2025-03-01 DOI:10.1016/j.rechem.2025.102150

Bhanuprakash C. Narasimhachar , Akshay Ravish , Narasimha M. Beeraka , Baburajeev Chumadathil Pookunoth , Shreeja Basappa , Divakar Vishwanath , Kanchugarakoppal S. Rangappa , Omantheswara Nagaraja , Mahendra Madegowda , Paduvalahippe Gowdegowda Chandrashekara , Basappa Basappa

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Abstract

Background

Heterocycles are vital in medicinal chemistry due to their diverse pharmacological activities against various diseases. The development of innovative synthetic methods for heterocycles is ongoing, aiming to explore their full therapeutic potential. The epidermal growth factor receptor (EGFR) is a key target in breast cancer (BC) treatment due to its significant role in disease progression.

Objective

This study aims to develop novel heterocyclic compounds containing benzimidazole, pyrimidine, and triazole derivatives, designed to target EGFR in breast cancer cells.

Methods

The synthesis of the heterocyclic compounds was carried out using a one-pot CuI-catalyzed aryl amination followed by a Huisgen 1,3-dipolar cycloaddition reaction. The cytotoxic effects of the synthesized compounds were assessed using IC₅₀ assays against MCF-7 breast cancer cells, with Tamoxifen and Doxorubicin as internal controls. Molecular docking studies were conducted to explore the binding interactions within the EGFR ATP-binding site. Further, molecular dynamics (MD) simulations were performed for 100 ns to validate the stability and interactions of the active compounds.

Results

Compounds 6a and 6b demonstrated significant cytotoxic activity with IC₅₀ values of 29.62 μM and 41.8 μM, respectively. In silico docking revealed that both compounds fit well into the ATP-binding site of EGFR, showing binding affinities of −7.27 kcal/mol for 6a and − 7.45 kcal/mol for 6b. MD simulations confirmed the stability of these interactions, with 6a forming a more stable complex, suggesting its potential as a more effective EGFR inhibitor.

Conclusion

The newly synthesized heterocyclic compounds exhibit potent cytotoxic effects against MCF-7 breast cancer cells and strong binding affinities to EGFR, indicating their potential as therapeutic agents. These findings warrant further investigation and optimization through preclinical and clinical studies to enhance their therapeutic efficacy against breast cancer.

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