“…The 13 C‐NMR ((D 6 )DMSO, 125 MHz) and DEPT spectra gave 25 carbon resonances, including one methyl, three methylenes (sp 3 hybridized), thirteen methines (eight sp 2 hybridized and five sp 3 hybridized), and eight quaternary carbons (sp 2 hybridized). Detailed analyses of above 25 carbon signals displayed that 15 carbons were due to one flavonoid skeleton, six carbons to one glucuronate moiety, and four carbons to one butyl group, respectively. In the HMBC experiment ( Figure ), the long‐range correlations from δ (H) 12.83 (1H, s, 5‐OH) to δ (C) 161.6 (C(5)), δ (H) 5.33 (1H, d, J = 7.3, H–C(1″)) to δ (C) 163.1 (C(7)) and δ (H) 4.04 – 4.15 (2H, m, H–C(1‴)) to δ (C) 169.2 (C(6″)) confirmed the hydroxy group, glucuronate ester moiety, and butyl group were attached to C(5), C(7), and C(6″), respectively.…”