Affiliation:
1. Department of Hair Care and Beauty Services, Yeşilyurt Vocational School Malatya Turgut Özal University Malatya Turkey
2. Department of Chemistry, Faculty of Sciences Çankırı Karatekin University Çankırı Turkey
3. Department of Biostatistics and Medical Informatics, Faculty of Medicine Karadeniz Technical University Trabzon Turkey
4. Department of Chemistry, Faculty of Art and Sciences Gaziantep University Gaziantep Turkey
Abstract
AbstractDiabetes mellitus is one of the most critical health problems affecting the quality of life of people worldwide, especially in developing countries. According to the World Health Organization reports, the number of patients with diabetes is approximately 420 million, and this number is estimated to be 642 million in 2040. There are 2 main types of diabetes: Type 1 (T1DM), where the body cannot produce enough insulin, and Type 2 (T2DM), where the body cannot use insulin properly. Patients with T1DM are treated with insulin injections while oral glucose‐lowering drugs are used for patients with T2DM. Oral antihyperglycemic drugs used in the treatment of type 2 diabetes mellitus have different mechanisms. Among these, α‐Glucosidase and α‐amylase inhibitors are one of the most important inhibitors. The antidiabetic effect of the chalcones, which show rich activity, draws attention. This research aims to synthesize chalcone derivatives that could show potential antidiabetic activity. In this study, the inhibitory activity of the chalcone compounds (4a‐4g, 5a‐5g) was tested against α‐glucosidase and α‐amylase enzymes. Besides, molecular modeling was utilized to predict potential interactions of the synthesized compounds that exhibit inhibitory effects. In both in vitro and in silico studies, the analyses revealed that compound 5e exhibits strong inhibitory effects against α‐glucosidase enzymes (Binding energy: −7.75 kcal/mol, IC50: 28.88 μM). Additionally, compound 4f demonstrates encouraging inhibitory effects against α‐Amylase (Binding energy: −11.08 kcal/mol, IC50: 46. 21 μM).
Subject
Molecular Biology,Structural Biology
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