Investigation of α-glucosidase and α-amylase inhibitory effects of phenoxy chalcones and molecular modeling studies

IF 2.3 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Bedriye Seda Kurşun-Aktar, Şevki Adem, Gizem Tatar-Yilmaz, Zeyad Adıl Hameed Hameed, Emine Elçin Oruç-Emre
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Abstract

Diabetes 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).

苯氧基查尔酮对α-葡萄糖苷酶和α-淀粉酶抑制作用的研究和分子模型研究。
糖尿病是影响全世界人民,特别是发展中国家人民生活质量的最严重的健康问题之一。根据世界卫生组织的报告,糖尿病患者人数约为4.2亿,预计2040年将达到6.42亿。糖尿病主要有两种类型:1型(T1DM)和2型(T2DM),前者身体不能产生足够的胰岛素,后者身体不能正确使用胰岛素。T1DM患者接受胰岛素注射治疗,而T2DM患者则使用口服降糖药物。口服抗高血糖药物用于治疗2型糖尿病有不同的机制。其中,α-葡萄糖苷酶和α-淀粉酶抑制剂是最重要的抑制剂之一。查尔酮的抗糖尿病作用,显示出丰富的活性,引起了人们的注意。本研究旨在合成具有潜在抗糖尿病活性的查尔酮衍生物。在本研究中,测试了查尔酮化合物(4a-4g,5a-5g)对α-葡萄糖苷酶和α-淀粉酶的抑制活性。此外,还利用分子模型预测了合成的具有抑制作用的化合物的潜在相互作用。在体外和计算机研究中,分析表明,化合物5e对α-葡萄糖苷酶表现出强烈的抑制作用(结合能:-7.75 kcal/mol,IC50:28.88 μM)。此外,化合物4f对α-淀粉酶表现出令人鼓舞的抑制作用(结合能:-11.08 kcal/mol,IC50:46。21 μM)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Molecular Recognition
Journal of Molecular Recognition 生物-生化与分子生物学
CiteScore
4.60
自引率
3.70%
发文量
68
审稿时长
2.7 months
期刊介绍: Journal of Molecular Recognition (JMR) publishes original research papers and reviews describing substantial advances in our understanding of molecular recognition phenomena in life sciences, covering all aspects from biochemistry, molecular biology, medicine, and biophysics. The research may employ experimental, theoretical and/or computational approaches. The focus of the journal is on recognition phenomena involving biomolecules and their biological / biochemical partners rather than on the recognition of metal ions or inorganic compounds. Molecular recognition involves non-covalent specific interactions between two or more biological molecules, molecular aggregates, cellular modules or organelles, as exemplified by receptor-ligand, antigen-antibody, nucleic acid-protein, sugar-lectin, to mention just a few of the possible interactions. The journal invites manuscripts that aim to achieve a complete description of molecular recognition mechanisms between well-characterized biomolecules in terms of structure, dynamics and biological activity. Such studies may help the future development of new drugs and vaccines, although the experimental testing of new drugs and vaccines falls outside the scope of the journal. Manuscripts that describe the application of standard approaches and techniques to design or model new molecular entities or to describe interactions between biomolecules, but do not provide new insights into molecular recognition processes will not be considered. Similarly, manuscripts involving biomolecules uncharacterized at the sequence level (e.g. calf thymus DNA) will not be considered.
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