“…The above NMR spectroscopic data suggested that 1 was an eudesmane-type sesquiterpenoid lactone, which has been widely discovered from this genus. [4][5][6][7][8] Comparison of NMR data of 1 with those of neolitacumone B (7) 15 indicated that 1 differed from 7 by the presence of a methyl (δ H 0.93, d, J = 6.0 Hz and δ C 19.8) and a methine (δ H 1.48, m and δ C 31.6) instead of one terminal double bond in 7, which was reasonable to assume that 1 is the 4,15-dihydrogenation derivative of 7. In the HMBC spectrum (Figure 1), the correlations of Me-15 (δ H 0.93) with C-3 (δ C 33.8), C-4 (δ C 31.6), and C-5 (δ C 50.6) were observed, which confirmed the above assumption.…”