“…Chemical structures of the isolated compounds.4,6-Dihydroxy-7-isobutyryl-5-prenyl-2(3H)-benzofuranone (4): White crystal (CHCl 3 ); m. p. 148 -150°C; UV (MeOH): λ max (log ε) = 240 (3.67), 280 (3.80), 332 (3.13) nm; [α] D -8 (c 0.2, CHCl 3 ); IR (KBr): ν max = 3453, 1803, 1630, 1604 cm -1 ; 1 H-NMR (CDCl 3 , 300 MHz): δ = 13.84 (brs, 6-OH), 6.60 (brs, 4-OH), 5.27 (1H, t, J = 6.6 Hz, H-2′), 3.70 (1H, sept, J = 6.6 Hz, H-9),3.62 (2H, s, H-3), 3.43 (2H, d, J = 6.6 Hz, H-1′), 1.84 (3H, s, H-5′), 1.79 (3H, s, H-4′), 1.21 (6H, d, J = 6.6 Hz, H-10,11); 13 C-NMR (CDCl 3 , 75 MHz): δ = 208.4 (s, C-8), 173.5 (s, C-2), 163.0 (s, C-6), 156.8 (s, C-4), 153.7 (s, C-7a), 137.2 (s, C-3′), 120.9 (d, C-2′), 109.1 (s, C-5), 100.7 (s, C-7), 100.4 (s, C-3a), 38.6 (d, C-9), 29.7 (t, C-3), 25.8 (q, C-4′), 21.8 (t, C-1′), 18.9 (q, C-10, 11), 17.9 (q, C-5′); EI-MS: m/z ( % rel. int.)…”