“…Fractions 5 to 7 (200 mg) were combined and further chromatographed over Si gel (elution with Cyclohexane-EtOAc 100:0 to 0:100 and EtOAc-MeOH 80:20) and yielded 25 fractions. Further semi-preparative HPLC using an inverse phase column (Kromasil, 5 Am 60 2, 250*10) with a water-CH 3 CN gradient yielded 1,6-dihydroxyxanthone (8) (10 mg, 0.11%, Rt 17.0 min) (Yang et al, 2001) and pancixanthone A (9) (1.3 mg, 0.014%, Rt 23.5 min) (Ito et al, 1996). Crystallization of the fourteenth fraction (70 mg) in CH 3 CN gave isocudraniaxanthone B (10) (50 mg, 0.54%) (Kobayashi et al, 1997).…”