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某物种乙醇提取物的气相色谱-质谱联用分析:肥胖症的网络药理学分析见解

GC-MS analysis of an ethanolic extract of species: a network pharmacology analysis insight towards obesity.

作者信息

Gnanamurthy Priyadharshini, Narasimhan Manoj K, Sabarathinam Sarvesh

机构信息

Department of Genetic Engineering, School of Bioengineering, College of Engineering & Technology, SRM Institute of Science & Technology, Kattankulathur, Chennai, Tamil Nadu, 603203, India.

Drug Testing Laboratory, Interdisciplinary Institute of Indian System of Medicine (IIISM), SRM Institute of Science & Technology, SRM IST, Kattankulathur, Chennai, Tamil Nadu, 603203, India.

出版信息

Future Sci OA. 2024 May 15;10(1):FSO940. doi: 10.2144/fsoa-2023-0202. eCollection 2024.

Abstract

In this study, we have selected two different plants, (Rama tulsi) (OTRT) and (Krishna tulsi) (OTKT). In the present investigation, ethanol was used as a solvent to estimate the bioactive compounds present in it through gas chromatography-mass spectrometry (GC-MS). Based on the GC-MS data benzenepropanoic acid, 3-methoxy-alpha,4-bis[(trimethylsilyl)oxy was found to be the potent compound in OTRT (MW: 428.74 g/mol) and methyl 3-(4-benzyloxy-3,5-dimethoxyphenyl)-2-methylpropanoate in OTKT (MW: 342.39 g/mol). To estimate its pharmacological application, an integrated Network Pharmacology approach is performed toward the disease target obesity. From the protein-protein interaction from the string database, SRC, BCL2, EGFR, MTOR, CDK1, ERBB2, MAPK1, FYN, AR and MAPK14 are the top-ranked targets.

摘要

在本研究中,我们选取了两种不同的植物,即(罗勒)(OTRT)和(黑罗勒)(OTKT)。在本次调查中,乙醇被用作溶剂,通过气相色谱 - 质谱联用仪(GC - MS)来评估其中存在的生物活性化合物。基于GC - MS数据,发现3 - 甲氧基 - α,4 - 双[(三甲基甲硅烷基)氧基]苯丙酸是OTRT中的有效化合物(分子量:428.74 g/mol),而3 - (4 - 苄氧基 - 3,5 - 二甲氧基苯基) - 2 - 甲基丙酸甲酯是OTKT中的有效化合物(分子量:342.39 g/mol)。为评估其药理学应用,针对疾病靶点肥胖症采用了综合网络药理学方法。从STRING数据库的蛋白质 - 蛋白质相互作用来看,SRC、BCL2、EGFR、MTOR、CDK1、ERBB2、MAPK1、FYN、AR和MAPK14是排名靠前的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/749a/11140659/9e34e82bfef5/IFSO_A_2340890_F0001_C.jpg

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