通过实验和计算技术分离、鉴定和研究曲霉次生代谢物†。

IF 3.9 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY RSC Advances Pub Date : 2024-11-15 DOI:10.1039/D4RA03674C
Zafar Ali Shah, Khalid Khan, Tanzeel Shah, Nasir Ahmad and Asad Khan
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引用次数: 0

摘要

众所周知,真菌代谢物具有广泛的治疗作用。在这种情况下,对曲霉菌株(FCBP-DNA-1266)的次生代谢物和体内活性进行了研究。结果分离出了萘-γ-吡喃酮(aurasperone B)和一种甾醇(麦角甾醇),并利用先进的光谱技术(如 1H NMR 和 13C NMR)对其进行了表征。利用动物模型对分离出的代谢物进行了体内抗炎和镇痛活性评估。研究表明,这两种代谢物都具有显著的药理作用(P ≤ 0.05),且呈剂量依赖性。此外,我们还采用了硅学分析来辅助体内抗炎活性,分子对接结果与实验结果一致。我们首次展示了aurasperone B的药理活性和二维核磁共振,这将有助于揭示非曲霉次生代谢产物的生物活性潜力。
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Isolation, characterization and pharmacological investigations of secondary metabolites from Aspergillus ficuum via experimental and computational techniques†

Fungal metabolites are known for their broad therapeutic effects. In this context, the fungal strain of Aspergillus ficuum (FCBP-DNA-1266) was examined for its secondary metabolites and in vivo activities. This led to the isolation of naphtho-gamma-pyrone (aurasperone B) and a sterol (ergosterol), characterized using advanced spectroscopic techniques such as 1H NMR and 13C NMR. The isolated metabolites were evaluated for their in vivo anti-inflammatory and analgesic activities utilizing an animal model. The study showed that both metabolites have significant pharmacological effects (P ≤ 0.05) in a dose-dependent manner. In addition, in silico analysis was employed to aid the in vivo anti-inflammatory activity and the molecular docking results were in agreement with the experimental findings. For the first time, we present the pharmacological activities and 2D NMR of aurasperone B, which will shed light on the bioactive potential of secondary metabolites of Aspergillus ficuum.

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来源期刊
RSC Advances
RSC Advances chemical sciences-
CiteScore
7.50
自引率
2.60%
发文量
3116
审稿时长
1.6 months
期刊介绍: An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.
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