Synthesis, Characterization, Biological Evaluation and Molecular Docking Studies of New Oxoacrylate and Acetamide on HeLa Cancer Cell Lines

Yükleniyor...
Küçük Resim

Tarih

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

Bentham Scıence Publ Ltd

Erişim Hakkı

info:eu-repo/semantics/openAccess

Özet

Background: In recent years, the discovery and development of new drugs play a critical role in cancer therapy.Objective: In this study, the effect of MPAEA and p-acetamide on cellular toxicity and on silico in HeLa cancer cells have been investigated.Methods: In this study, 2-choloro-N-(4-methoxyphenyl)acetamide (p-acetamide) and 2-(4methoxyphenylamino)-2-oxoethyl acrylate (MPAEA) have been synthesized and characterized by FTIR, H-1, and C-13-NMR. Cytotoxicity of p-acetamide and MPAEA have been investigated by XTT cell proliferation assay on the HeLa cell line. IC50 values of p-acetamide and MPAEA have been identified on the HeLa cell line. Further, a molecular docking study was carried out by Autodock Vina using BCL-2 (PDB ID: 4MAN), BCL-W (PDB ID: 2Y6W), MCl-1 (PDB ID: 5FDO) AKT (PDB ID: 4GV1) and BRAF (PDB ID: 5VAM) as a possible apoptotic target for anticancer activity.Results: According to the obtained results, MPAEA and p-acetamide were successfully synthesized and characterized. The interactions between ligands and anti-apoptotic proteins were evaluated by molecular docking, and their free energy of binding was calculated and used as a descriptor.Conclusion: In vitro and in silico, the results demonstrated that MPAEA had potent anticancer activity on the HeLa cell line.

Açıklama

Anahtar Kelimeler

Synthesis and characterization, antiproliferative activity, hela cell line, molecular docking, anti-apoptotic proteins, MPAEA

Kaynak

Current Computer-Aıded Drug Desıgn

WoS Q Değeri

Scopus Q Değeri

Cilt

17

Sayı

6

Künye

Çankaya, N., İzdal, M., & Azarkan, S. Y. (2021). Synthesis, Characterization, Biological Evaluation and Molecular Docking Studies of New Oxoacrylate and Acetamide on HeLa Cancer Cell Lines. Current Computer-Aided Drug Design, 17(6), 838-848.

Onay

İnceleme

Ekleyen

Referans Veren