Salidroside: A review of its recent advances in synthetic pathways and pharmacological properties
出版年份 2021 全文链接
标题
Salidroside: A review of its recent advances in synthetic pathways and pharmacological properties
作者
关键词
Salidroside, Synthesis, Pharmacology, Mechanisms, Pharmacokinetics, Toxicology
出版物
CHEMICO-BIOLOGICAL INTERACTIONS
Volume 339, Issue -, Pages 109268
出版商
Elsevier BV
发表日期
2021-02-21
DOI
10.1016/j.cbi.2020.109268
参考文献
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注意：仅列出部分参考文献，下载原文获取全部文献信息。- Salidroside protects against ox-LDL-induced endothelial injury by enhancing autophagy mediated by SIRT1-FoxO1 pathway
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- Salidroside rescued mice from experimental sepsis through anti-inflammatory and anti-apoptosis effects
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- Salidroside attenuates lipopolysaccharide (LPS) induced serum cytokines and depressive-like behavior in mice
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- Salidroside inhibits the growth of human breast cancer in vitro and in vivo
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- Salidroside Protects against Cadmium-Induced Hepatotoxicity in Rats via GJIC and MAPK Pathways
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- Salidroside Ameliorates Cd-Induced Calcium Overload and Gap Junction Dysfunction in BRL 3A Rat Liver Cells
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- Sequential release of salidroside and paeonol from a nanosphere-hydrogel system inhibits ultraviolet B-induced melanogenesis in guinea pig skin
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- Salidroside stimulated glucose uptake in skeletal muscle cells by activating AMP-activated protein kinase
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