“…This compound was then subjected to NMR analysis: 1 H-NMR (500 MHz, CDCl 3 ): δ5.27 (1H, m, H-12), 3.25 (1H, dd, J = 15.0, 5.9 Hz), 2.81 (1H, dd, J = 12.3, 5.5 Hz), 1.13 (3H, s), 1.06 (3H, s), 0.98 (3H, s), 0.92 (3H, s), 0.90 (3H, s), 0.77 (3H, s), 0.74 (3H, s); 13 C-NMR (125 MHz, CDCl 3 ): δ38.4 (C-1), 27.1 (C-2), 79.0 (C-3), 38.7 (C-4), 55.2 (C-5), 18.3 (C-6), 32.9 (C-7), 39.3 (C-8), 47.6 (C-9), 37.1 (C-10), 22.9 (C-11), 122.6 (C-12), 143.6 (C-13), 41.6 (C-14), 27.7 (C-15), 23.5 (C-16), 46.5 (C-17), 40.9 (C-18), 45.9 (C-19), 30.6 (C-20), 33.8 (C-21), 32.4 (C-22), 28.1 (C-23), 15.3 (C-24), 15.5 (C-25), 17.1 (C-26), 25.9 (C-27), 183.4 (C-28), 33.4 (C-29), 23.4 (C-30). Based on comparisons with published data (13), the purified compound was identified as (3β)-3-hydroxyolean-12-en-28-oic acid (oleanolic acid, OA). The cytotoxic activity of OA was analyzed in various human cancer cell lines.…”