Unlocking the anti-infective potential of phytoconstituents derived from Euphorbia neriifolia Linn.: Molecular docking, pharmacokinetics, drug-likeliness, and toxicological evaluations

Md. Jamal Hossain , Md. Shohel Hossen , Md Anisur Rahman , Md. Hosan Khan , Joy Johon Roy , Hujjout Ullah , Kazi Md. Asraful Islam , Morium Benta Mohasin , Mst. Monisha Akter Mimi , Marsia Haque Meghla , Md. Rejaul Karim Bhuiya , Utsha Barua , Mohammad A. Rashid
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Abstract

Background and aim

Growing resistance to conventional antibiotics has promoted interest in bioactive molecules derived from plants that may have anti-infective effects. Euphorbia neriifolia has long been used for its therapeutic benefits, exhibited potential as a source of antimicrobial natural products. The present research aimed to investigate the molecular interactions of several lead compounds of E. neriifolia focusing on antimicrobial effects, pharmacokinetics and toxicological properties, including their drug-likeliness profiles.

Methods

A total of 18 lead compounds of E. neriifolia were retrieved from the literature based on their antimicrobial properties. PyRx, PyMol, and Discovery Studio (v4.5) were used for molecular docking against CTX-M-9 Beta-lactamase, dihydrofolate reductase enzyme, DNA gyrase, and OmpF Porin for antibacterial properties; 3CL protease, RNA dependent RNA polymerase (RdRp), and spike protein for anti-SARS-CoV-2 potential; neuraminidase and hemagglutinin H1 for anti-influenza; old yellow enzyme for antifungal; and HIV-1 reverse transcriptase for anti-HIV activities. Absorption, distribution, metabolism, excretion, and toxicity (ADME/T) with drug likeliness properties were analyzed using pkCSM and Swiss ADME online tools.

Results

Among the 18 compounds, rutin and tulipanian exhibited higher binding affinities against most targets than their corresponding standard ligands. Most compounds, including rutin, friedelin, lupenone, beta-amyrin, and tulipanin, showed OmpF Porin protein inhibitory properties. At least 10 compounds, including quercetin, rutin, tulipanin, afzelin, pachypodol, and euphonerin A-D, exhibited higher binding affinities against the fungal old yellow enzyme, revealing promising antifungal properties. Furthermore, most compounds exerted favorable ADME/T properties and showed drug likeliness by obeying the Lipinski rule of five.

Conclusion

Based on the current findings, this study offers the possibility of making a natural remedy for treating microbial infections from E. neriifolia. These results can be considered as the groundwork for developing plant-based medicinal compounds and conducting further in silico and experimental validation.
解锁大戟植物成分的抗感染潜能。分子对接、药代动力学、药物可能性和毒理学评价
背景和目的对常规抗生素的耐药性日益增长,促使人们对从植物中提取的具有抗感染作用的生物活性分子产生了兴趣。大戟叶长期以来一直被用于其治疗效益,表现出潜在的抗菌天然产品的来源。本研究主要从拮抗作用、药代动力学和毒理学特性及其药物可能性等方面研究了苦参中几种先导化合物的分子相互作用。方法从文献中筛选出18个主要抑菌成分。利用PyRx、PyMol和Discovery Studio (v4.5)对CTX-M-9 β -内酰胺酶、二氢叶酸还原酶、DNA旋切酶和OmpF Porin进行分子对接,测定其抗菌性能;3CL蛋白酶、RNA依赖性RNA聚合酶(RdRp)和刺突蛋白抗sars - cov -2潜能神经氨酸酶和血凝素H1抗流感;抗真菌老黄酶;以及HIV-1逆转录酶的抗hiv活性。使用pkCSM和瑞士ADME在线工具分析吸收、分布、代谢、排泄和毒性(ADME/T)与药物似然特性。结果在18个化合物中,芦丁和郁金香花对大多数靶标的结合亲和力高于其对应的标准配体。大多数化合物,包括芦丁、叶黄素、豆烯酮、β -amyrin和tulipanin,都表现出抑制OmpF Porin蛋白的特性。至少有10种化合物,包括槲皮素、芦丁、花脂素、黄芩苷、肿脚酚和euphonerin A-D,对真菌老黄酶表现出较高的结合亲和力,显示出有希望的抗真菌特性。此外,大多数化合物具有良好的ADME/T特性,并符合Lipinski五法则。结论基于目前的研究结果,本研究为开发一种天然药物治疗毛蕊草微生物感染提供了可能。这些结果可以被认为是开发植物基药物化合物和进行进一步的硅和实验验证的基础。
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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