Molecular docking and admet properties of anacardium occidentale methanolic nut extract against inflammatory, oxidative and apoptotic markers of diabetes

Ajao Folasade Omobolanle, Iyedupe Marcus Olaoye, Adegbola Raphael Oneosinina, Kalejaiye Noheem Olaolu, Adelusi Temitope Isaac
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Abstract

Background. The contemporary antidiabetic drugs have side effects and adverse reactions. This demand to search for less toxic and effective treatments for diabetes from medicinal plants using computational methods. The present research investigated the molecular docking of Anacadium occidentale nut methanolic extract compounds with selected proteins related to diabetes and the compounds’ AMDET properties. Material and Methods. The compounds were identified using Gas chromatography-mass spectrometry analysis. The compounds'2-dimensional structure was retrieved from the PubChem compound database. Three-dimensional crystallographic structure of selected proteins; B-cell-lymphoma-2 (Bcl-2), caspase-3, glucocorticoids, interleukin-1β, myeloperoxidase and tumor necrosis factor-alpha (TNF-α) was downloaded from Protein Data Bank. Molecular docking was performed using Autodoc kvina and the active site of binding interactions was detected with the Computed Atlas of Surface Topography of proteins (CAST-P). The compounds' drug-likeness, physicochemical and ADMET were evaluated using molininspiration and admetSAR online tools. Results. Ten compounds were identified from the Anacardium occidentale nut methanolic extract. All the compounds exhibited drug-likeness properties with violation of one Lipinski’s rule. Two compounds, oleic acid and 3-(p-methoxyphenyl)-propionic acid exhibited the best binding energy with the active receptors site of Bcl-2, caspase-3, TNF-α and glucocorticoid. Also, tridecanoic acid exhibited good binding energy with the active site of glucocorticoid receptors. Only 3-(p-methoxyphenyl)-propionic acid exhibited moderate binding energy with the active receptors site of interleukin-1β and myeloperoxidase. All the compounds displayed excellent ADMET properties. Conclusions. Antidiabetic drugs with the least side effects could be explored from these compounds.
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西心梗甲醇坚果提取物对糖尿病炎症、氧化和凋亡标志物的分子对接及适应性研究
背景。目前的降糖药存在副作用和不良反应。这就要求利用计算方法从药用植物中寻找毒性更小且有效的糖尿病治疗方法。本研究研究了西方阿纳金坚果甲醇提取物化合物与糖尿病相关蛋白的分子对接及其AMDET特性。材料和方法。采用气相色谱-质谱法对化合物进行鉴定。化合物的二维结构从PubChem化合物数据库中检索。选定蛋白质的三维晶体结构;从蛋白质数据库下载b细胞淋巴瘤-2 (Bcl-2)、caspase-3、糖皮质激素、白细胞介素-1β、髓过氧化物酶和肿瘤坏死因子-α (TNF-α)。使用Autodoc kvina进行分子对接,并使用蛋白质表面形貌计算机图谱(CAST-P)检测结合相互作用的活性位点。利用molininspiration和admetSAR在线工具对化合物的药物相似性、理化性质和ADMET进行了评价。结果。从西心果甲醇提取物中鉴定出10个化合物。所有化合物都表现出与药物相似的性质,但违反了一条利宾斯基规则。油酸和3-(对甲氧基苯基)-丙酸两种化合物与Bcl-2、caspase-3、TNF-α和糖皮质激素活性受体位点的结合能最好。此外,三烷酸与糖皮质激素受体活性位点表现出良好的结合能。只有3-(对甲氧基苯基)-丙酸与白细胞介素-1β和髓过氧化物酶活性受体位点表现出中等的结合能。所有化合物均表现出优异的ADMET性能。结论。从这些化合物中可以开发出副作用最小的抗糖尿病药物。
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