| Literature DB >> 31655431 |
Qiong Wu1, Ruiying Wang2, Yang Shi1, Wenchao Li1, Meng Li3, Peng Chen1, Bowen Pan1, Qing Wang1, Caifeng Li4, Jianbing Wang5, Guibo Sun2, Xiaobo Sun2, Hongzheng Fu6.
Abstract
Panaxatriol (PT) is a natural product derived from ginseng that possesses cardioprotective effects in isolated rat hearts. To develop more potent therapeutic agents against myocardial ischemia/reperfusion (MI/R) injury from natural products, a novel series of heterocycle ring-fused panaxatriol derivatives were designed and synthesized. In vitro results showed that approximately half of them exhibited increased cytoprotective activity compared with PT in a cardiomyocyte model of oxygen-glucose deprivation and reperfusion (OGD/R) injury. Furthermore, the in vitro activity of the representative derivative, compound 18, was also confirmed in a rat model of MI/R injury. In vivo results showed that 18 can markedly reduce myocardial infarction size, decrease circulating cardiac troponin I (cTnI) leakage, and alleviate cardiac tissue damage in the rats. Therefore, these findings provide the basis for further development of novel anti-MI/R injury agents.Entities:
Keywords: Heterocyclic compounds; Ischemia/reperfusion injury; Panaxatriol; Structure-activity relationships; Synthesis
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Year: 2019 PMID: 31655431 DOI: 10.1016/j.ejmech.2019.111729
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514