Generation of Radical Species from Dihydropyrazines Having DNA Strand-Breakage Activity and Other Characteristics
Author:
Affiliation:
1. Faculty of Pharmaceutical Sciences, Sojo University
2. Department of Biochemistry and Isotope, Tokyo Metropolitan Institute of Gerontology
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
https://www.jstage.jst.go.jp/article/cpb/60/5/60_5_639/_pdf
Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Dihydropyrazine induces endoplasmic reticulum stress and inhibits autophagy in HepG2 human hepatoma cells;The Journal of Toxicological Sciences;2024
2. Oxidative stress and cellular toxicity induced by dihydropyrazine: a comparative study with other Maillard reaction products;The Journal of Toxicological Sciences;2023
3. Dihydropyrazine suppresses TLR4-dependent inflammatory responses by blocking MAPK signaling in human hepatoma HepG2 cells;The Journal of Toxicological Sciences;2022
4. Molecular mechanism of dihydropyrazine-induced cytotoxicity: the possibility of an independent pathway from the receptor for advanced glycation end products;The Journal of Toxicological Sciences;2021
5. The effect of dihydropyrazines on lipopolysaccharide-stimulated human hepatoma HepG2 cells via regulating the TLR4-MyD88-mediated NF-κB signaling pathway;The Journal of Toxicological Sciences;2020
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