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SCI國際期刊 - Fitoterapia. 2015, 102: 115-119.4
http://www.lantyng.url.tw/custom_70762.html SCI國際期刊 - Fitoterapia. 2015, 102: 115-119. SCI國際期刊 - Fitoterapia. 2015, 102: 115-119. FitoterapiaVolume 102, April 2015, Pages 115-119Anti-cancer agents derived from solid-state fermented Antrodia camphorata myceliumAbstractThree new ubiquinone derivatives, antrocamol LT1, antrocamol LT2, and antrocamol LT3, along with two known compounds, were isolated from Antrodia camphorata (Polyporaceae) mycelium. The structures of these compounds were established on the basis of extensive 1D and 2D NMR spectroscopic analyses. These ubiquinones exhibited selective cytotoxicities against five human cancer cell lines (CT26, A549, HepG2, PC3 and DU-145) with IC50 values ranging from 0.01 to 1.79 μΜ.Graphical abstractThree new ubiquinone derivatives, antrocamol LT1, LT2 and LT3, were isolated from Antrodia camphorate mycelium and exhibited potential cytotoxicities against five human cancer cell lines.
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Fitoterapia
Volume 102, April 2015, Pages 115-119

Anti-cancer agents derived from solid-state fermented Antrodia camphorata mycelium


Abstract

Three new ubiquinone derivatives, antrocamol LT1, antrocamol LT2, and antrocamol LT3, along with two known compounds, were isolated from Antrodia camphorata (Polyporaceae) mycelium. The structures of these compounds were established on the basis of extensive 1D and 2D NMR spectroscopic analyses. These ubiquinones exhibited selective cytotoxicities against five human cancer cell lines (CT26, A549, HepG2, PC3 and DU-145) with IC50 values ranging from 0.01 to 1.79 μΜ.


Graphical abstract

Three new ubiquinone derivatives, antrocamol LT1, LT2 and LT3, were isolated from Antrodia camphorate mycelium and exhibited potential cytotoxicities against five human cancer cell lines.


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