2015
DOI: 10.1016/j.jep.2015.11.018
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Anti-H1N1 virus, cytotoxic and Nrf2 activation activities of chemical constituents from Scutellaria baicalensis

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Cited by 96 publications
(59 citation statements)
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“…Additionally, in one report of 2015, a total of 30 compounds were isolated and identified from Scutellaria baicalensis, and five of them including baicalin, baicalein, wogonin, chrysin and oroxylin A showed significant anti-H1N1 activity with IC 50 values of 7.4, 7.5, 2.1, 7.7 and 12.8 lm, respectively. [72] It was worth mentioning that the cytotoxic activity was the strongest at 10 lm, and at this time, the inhibition rate was as high as 61.2%.…”
Section: Antibacterial and Antiviral Effectsmentioning
confidence: 87%
“…Additionally, in one report of 2015, a total of 30 compounds were isolated and identified from Scutellaria baicalensis, and five of them including baicalin, baicalein, wogonin, chrysin and oroxylin A showed significant anti-H1N1 activity with IC 50 values of 7.4, 7.5, 2.1, 7.7 and 12.8 lm, respectively. [72] It was worth mentioning that the cytotoxic activity was the strongest at 10 lm, and at this time, the inhibition rate was as high as 61.2%.…”
Section: Antibacterial and Antiviral Effectsmentioning
confidence: 87%
“…As a whole, aglycone forms, especially baicalein, exhibit high antioxidant activity . Moreover, their antiviral activity and, more importantly, antitumor activity has also been studied. Major flavones of the skullcap roots not only suppress the growth of the tumor cells themselves, but enhance the antitumor activity of other medications at the combined administration …”
Section: Introductionmentioning
confidence: 99%
“…The compounds 1, 34, 54, and 55 were chemically synthesized according to the reported method [25] by Hangzhou Yuhao Chemical Technology Co., Ltd . [26] Substrates 3-10, 13, 17, 18, 20, 22, 24-33, 36-38, 44-53, 56, 57, 59-64, 66-68 [26] Substrates 3-10, 13, 17, 18, 20, 22, 24-33, 36-38, 44-53, 56, 57, 59-64, 66-68 …”
Section: Experimental Section Materialsmentioning
confidence: 99%
“…Compounds 2, 11, 12, 14-16, 19, 21, 23, 35, 39-43, 58, 65, and 69 were isolated from Glycyrrhiza uralensis, G. inflata, G. glabra, and Scutellaria baicalensis in our laboratory. [26] Substrates 3-10, 13, 17, 18, 20, 22, 24-33, 36-38, 44-53, 56, 57, 59-64, 66-68, 70-96 were individually purchased from Shanghai YuanYe Biotechnology Co., Ltd. (Shanghai, China), Beijing Solarbio Science & Technology Co., Ltd (Beijing, China), Chengdu Must Bio-Technology Co., Ltd (Chengdu, China), and TargetMol (Shanghai, China). The prenyl donors, dimethylallyl diphosphate (DMAPP), geranyl diphosphate (GPP), farnesyl diphosphate (FPP), geranylgeranyl diphosphate (GGPP), and phytyl diphosphate (PPP), were chemically synthesized according to the literature.…”
Section: Experimental Section Materialsmentioning
confidence: 99%