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Anti-cancer agents derived from solid-state fermented Antrodia camphorata mycelium
I-Chuan Yen1, Chen-Wen Yao2, Mao-Tien Kuo3
1Graduate Institute of Medical Science, National Defense Medical Center, No. 161, Sec. 6, Minchuan East Road, Neihu District, Taipei City 114, Taiwan, ROC; School of Pharmacy, National Defense Medical Center, No. 161, Sec. 6, Minchuan East Road, Neihu District, Taipei City 114, Taiwan, ROC.
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 1.79μΜ.
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