“…Repeated column chromatography of the bioactive fractions resulted in the isolation of 10 compounds, out of which compounds 1e5 were new compounds and structures were established using IR, MS, 1D and 2D NMR (HSQC, HMBC, COSY, and NOESY) spectroscopic techniques. The other five known compounds were identified as Piscidinone A (6), 11 Piscidinol C (7), 9d Piscidinol D (8), 6a Piscidinol E (9), 9e and Lupeol (10) 12 1.13, 1.16, 1.17, 1.28, 1.47, and 1.65 (3H each, s), which correlated with the carbons at d C 21. 4, 27.5, 18.8, 20.3, 26.8, 19.5, and 24.7 13 implied that their structures were closely related, with the marked difference being a presence of a carbonyl group at C-7 (B-ring) instead of an acetoxyl group.…”