“…IR (cm −1 ) ν: 3367, 1736, 1646, 896. 1 H NMR (600 MHz, in DMSO-d6), δ (ppm): 1.327 (m, 2H, C1-CH 2 ), 2.045 (brs, 1H, C2-CH 2 ), 1.999 (o, 1H, C2-CH 2 ), 3.353 (o, 1H, C3-CH-), 1.463 (o, 1H, C5-CH-), 2.182 (brs, 1H, C6-CH 2 ), 1.987 (brd, J = 6 Hz, 1H, C6-CH 2 ), 2.451 (t, 2H, C7-CH 2 ), 3.506 (o, 1H, C9-CH-), 2.433 (dd, J = 4.2, 2.4 Hz, 2H, C11-CH 2 ), 2.557 (dd, J = 12, 7.2 Hz, 2H, C12-CH 2 ), 7.10 (brs, 1H, C14-CH-), , 4.91 (brs, 2H, C15-CH 2 ), 4.595 (brs, 1H, C17-CH 2 ), 4.455 (brs, 1H, C17-CH 2 ), 1.599 (o, 3H, C18-CH 3 ), 4.207 (brs, 1H, C19-CH 2 ), 4.189 (brs, 1H, C19-CH 2 ), 0.71 (s, 3H, C20-CH 3 ), "o" denotes overlapping signals; 13 (Poonam et al, 2010) of the same compound, AB-2 was unambiguously identified as 14deoxyandrographolide ( Fig. 2).…”