木犀草素
小桶
化学
中医药
MAPK/ERK通路
药理学
PI3K/AKT/mTOR通路
传统医学
再生障碍性贫血
计算生物学
信号转导
生物化学
医学
类黄酮
生物
抗氧化剂
基因本体论
骨髓
基因表达
替代医学
病理
基因
内科学
作者
Wenjian Wei,Yuping Si,Zonghong Li,Xuewei Yin,Guodong Ma,Jing-Bo Shi,Changnian Li,Liming Yu,Wei Zheng,Yan Wang,Kui Liu,Ruirong Xu,Siyuan Cui
标识
DOI:10.1080/14786419.2024.2386126
摘要
To reveal the potential mechanism of the effect of Chinese Herbal Medicine Fuzi on Aplastic anaemia (AA) according to the network pharmacology approach and molecular docking. According to Ultra High Performance Liquid Chromatography Mass Spectrometry (UHPLC-MS/MS), 146 chemical ingredients of Fuzi were obtained. By SwissADME online system analysis, a total of 55 compounds such as Magnoflorine, Scutellarein, Luteolin and Gingerol may be the main active components of Fuzi and 145 common targets related to AA were predicted. 17 targets such as MAPK1, AKT1 and GRB2 were considered as hub targets. KEGG and GO enrichment analysis obtained 122 signalling pathways and 950 remarkable results. These results suggested that Fuzi exerted pharmacological effects on AA mainly by regulating PI3K-Akt, MAPK and JAK-STAT signalling pathways and epithelial cell proliferation, cell differentiation, regulate energy production and other biological processes. Meanwhile, molecular docking results showed that the hub targets had good binding ability with the main active ingredients.
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