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从 Ophiocoma dentata 中提取一种新型甾体衍生物的特性、计算机模拟和体外研究,作为治疗 COVID-19 的潜在药物。

Characterization, in-silico, and in-vitro study of a new steroid derivative from Ophiocoma dentata as a potential treatment for COVID-19.

机构信息

National Institute of Oceanography and Fisheries (NIOF), Cairo, Egypt.

Center of Excellence for Drug Preclinical Studies (CE-DPS), Pharmaceutical and Fermentation Industries Development Centre (PFIDC), City of Scientific Research and Technological Applications (SRTA-City), New Borg El Arab, Egypt.

出版信息

Sci Rep. 2022 Apr 7;12(1):5846. doi: 10.1038/s41598-022-09809-2.

DOI:10.1038/s41598-022-09809-2
PMID:35393477
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8991244/
Abstract

The medicinal potential of marine invertebrates' bioactive components that may act as anti-COVID-19 demonstrated promising results. Ophiocoma dentata, which is common in the Red Sea, is one such source. Therefore, this study aimed to isolate a new compound from the brittle star, Ophiocoma dentata, and evaluate its efficacy as anti-COVID-19 in-silico and in-vitro. Standard procedures were followed in order to assess the isolated compound's preliminary toxicity and anti-inflammatory properties. Computer virtual screening technology through molecular docking and ADMET studies was conducted as well as a new steroid derivative was isolated for the first time, named 5α-cholesta-4(27), 24-dien-3β, 23 β-diol. Investigation of the Anti-Covid-19 activity of the isolated compound using a Plaque reduction assay revealed 95% inhibition at a concentration of 5 ng/µl (12.48 µM). Moreover, this compound showed an IC of 11,350 ± 1500 ng/ml against the normal fibroblast cells, indicating its safety. Interestingly, this compound exhibited anti-inflammatory activity with an IC of 51.92 ± 0.03 μg/ml compared to a reference drug's IC of 53.64 ± 0.01 μg/ml, indicating that this compound is a potent anti-inflammatory. In silico data have proved that the isolated compound is a promising viral inhibitor against SARS-CoV2 and is thus recommended as a future nature preventive and curative antiviral drug.

摘要

海洋无脊椎动物生物活性成分的药用潜力可能具有抗 COVID-19 作用,已取得可喜的成果。棘皮动物 Ophiocoma dentata 在红海很常见,就是这样的一种来源。因此,本研究旨在从脆星 Ophiocoma dentata 中分离一种新化合物,并评估其作为抗 COVID-19 的体内和体外功效。为了评估分离化合物的初步毒性和抗炎特性,遵循了标准程序。进行了计算机虚拟筛选技术,包括分子对接和 ADMET 研究,并首次分离出一种新的甾体衍生物,命名为 5α-胆甾烷-4(27),24-二烯-3β,23β-二醇。通过蚀斑减少测定法研究分离化合物的抗 COVID-19 活性,在 5ng/µl(12.48µM)浓度下抑制率达到 95%。此外,该化合物对正常成纤维细胞的 IC 为 11,350±1500ng/ml,表明其安全性。有趣的是,与参考药物的 IC 为 53.64±0.01μg/ml 相比,该化合物表现出 51.92±0.03μg/ml 的抗炎活性,表明该化合物具有很强的抗炎作用。体内数据证明,分离的化合物是一种有前途的抗 SARS-CoV2 病毒抑制剂,因此建议将其作为未来的天然预防和治疗性抗病毒药物。

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