“…The H 2 O extracts were separately chromatographed using Diaion HP-20, YMC GEL ODS-AQ, MCI-gel CHP-20P, and Sephadex LH-20 with MeOH-H 2 O or ethanol (EtOH)-MeOH in a stepwise gradient mode. The fractions with similar high-performance liquid chromatography (HPLC) chromatograms were merged and further purified using column chromatography to obtain trapadin A (1), gallic acid (2) [19], methyl gallate (3) [19], vanillic acid (4) [19], brevifolincarboxylic acid (5) [20], ellagic acid (6) [21], urolithin A (7) [22], isourolithin A (8) [13], urolithin B (9) [11], urolithin M6 (10) [22], 1,2-di-O-galloyl-β-D-glucose (11) [23,24], 1,6-di-O-galloyl-β-D-glucose (12) [25], 1,2,3-tri-O-galloyl-β-D-glucose (13) [5,26], 1,2,6-tri-O-galloyl-β-D-glucose ( 14) [5,26], 1,2,3,6tetra-O-galloyl-β-D-glucose (15) [5,26], 1,2,3,4,6-penta-O-galloyl-β-D-glucose (16) [24,27], [28], tellimagrandin I (19) [26,29], tellimagrandin II (20) [5,26], cornusiin A (21) [30], rugosin D (22) [31], and (7 S,8 R)-dihydrodehydrodiconiferyl alcohol-9 -O-β-Dglucose (23) [5] (Figure 1). The known compounds 2-23 were identified by direct HPLC comparison with authentic standards and/or by comparing their spectral data with those reported in the literature.…”