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. 2016 Jul 8;14(7):130. doi: 10.3390/md14070130

Table 1.

NMR data and HMBC (heteronuclear multiple-bond correlation spectroscopy) correlations of compound 1 (CDCl3).

Position δC δH (m, J in Hz) HMBC (H→C) a
1 39.7, CH2 1.66, 0.79 (m) C-10
2 18.5, CH2 1.60, 1.44 (m) C-4, C-10
3 41.9 CH2 1.37, 1.11 (m) C-4
4 33.3 qC - -
5 56.5 CH 0.78 (m) C-4
6 18.0 CH2 1.59, 1.39 (m)
7 41.4 CH2 1.78, 0.92 (m) C-8
8 37.3 qC - -
9 58.3 CH 0.89 (m) C-10, C-12
10 37.4 qC - -
11 25.8 CH2 1.82, 1.55 (m) C-10, C-12
12 73.8 CH 3.82 (dd, 16.8, 6.6) C-9, C-11, C-13, C-25, C-26
13 44.6 qC - -
14 53.3 CH 1.25 (m) C-8, C-9, C-13, C-16, C-18
15 24.2 CH2 2.20, 1.63 (m) C-8, C-13, C-14, C-16, C-17
16 65.9 CH 5.67 (dd, 9.6, 7.2) C-15, C-17, C-20
17 126.1 qC - -
18 168.7 qC - -
19 95.5 CH 6.17 (s) C-17, C-18
20 170.8 qC - -
21 21.2 CH3 0.80 (s) C-4
22 33.2 CH3 0.84 (s) C-4
23 17.5 CH3 0.89 (s) C-7, C-8, C-9, C-14
24 16.1 CH3 0.84 (s) C-1, C-5, C-9, C-10
25 16.7 CH3 1.23 (s) C-12, C-13, C-14, C-18
26 169.8 qC - -
27 21.0 CH3 2.09 (s) C-26

a: HMBC correlations are from proton(s) stated to the indicated carbons.