Metabolite Profiling and In silico Studies to Elucidate the Antiinflammatory Properties of Pterocarpus Milbreadii

Q4 Pharmacology, Toxicology and Pharmaceutics Current Enzyme Inhibition Pub Date : 2024-01-12 DOI:10.2174/0115734080277468231129075038
P. Aba, Ismaila Onuche Odugbo
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Abstract

Pterocarpus milbreadii (PM), called Rosewood in English, is a leafy vegetable used in preparing soup and has also proven medicinal. This study aimed to evaluate the most abundant compound in the ethylacetate fraction of PM using Gas Chromatography-mass Spectrometry (GC-MS) and docking it against cyclooxygenase isoenzymes. The PM leaves were extracted with ethyl acetate using the cold maceration method. The extract was subjected to GC-MS assay. The spectra obtained were matched with NIST 17. AutoDock Vina was used to perform the molecular docking of the most abundant compound of PM and cyclooxygenase. Celecoxib was used as the standard ligand. The results of the study revealed that the ethyl acetate leaf extract of PM contained different phytochemicals, with hexadecenoic acid being the most abundant, with an intensity count of 9.5 x108 CPS. Docking of hexadecenoic acid and Celecoxib with COX-2 yielded binding energies of -6.7 and -7.7 kcal/mol, respectively, while with COX-1, the binding energies of -6.3 and -9.8 kcal/mol were respectively recorded. Hexadecenoic acid interacted with both COX-1 and COX-2 largely via Van der waals and pi-Alkyl bonds. Celecoxib made conventional hydrogen, carbon-hydrogen, halogen, pi-sigma, pi-alkyl interactions with the cyclooxygenase isoenzymes. It was concluded that hexadecenoic acid was the predominant phytochemical in the ethylacetate leaf extract of PM. The hexadecanoic acid ligand produced a better inhibitory effect on COX-2 compared to COX-1.
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通过代谢物轮廓分析和硅学研究阐明紫檀的抗炎特性
本研究旨在使用气相色谱-质谱法(GC-MS)评估紫檀叶乙酸乙酯馏分中含量最高的化合物,并将其与环氧酶酶基对接。采用冷浸渍法用乙酸乙酯萃取 PM 叶片,萃取液进行 GC-MS 分析。得到的光谱与 NIST 17 相匹配。研究结果表明,PM 的乙酸乙酯叶提取物中含有不同的植物化学物质,其中含量最高的是十六碳烯酸,其强度为 9.5 x108CPS。十六碳烯酸和塞来昔布与 COX-2 的对接结合能分别为-6.7 和-7.7 kcal/mol,而与 COX-1 的对接结合能分别为-6.3 和-9.8 kcal/mol。十六碳烯酸与 COX-1 和 COX-2 主要通过 Vander waerals 和 pi-Alkyl 键相互作用。结论是十六烯酸是 PM 乙酸乙酯叶提取物中最主要的植物化学物质。与 COX-1 相比,十六烷酸配体对 COX-2 产生了更好的抑制作用。
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来源期刊
Current Enzyme Inhibition
Current Enzyme Inhibition Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
CiteScore
1.30
自引率
0.00%
发文量
30
期刊介绍: Current Enzyme Inhibition aims to publish all the latest and outstanding developments in enzyme inhibition studies with regards to the mechanisms of inhibitory processes of enzymes, recognition of active sites, and the discovery of agonists and antagonists, leading to the design and development of new drugs of significant therapeutic value. Each issue contains a series of timely, in-depth reviews written by leaders in the field, covering a range of enzymes that can be exploited for drug development. Current Enzyme Inhibition is an essential journal for every pharmaceutical and medicinal chemist who wishes to have up-to-date knowledge about each and every development in the study of enzyme inhibition.
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