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. 2016 Dec 28;8(6):10071–10084. doi: 10.18632/oncotarget.14336

Table 2. 13C NMR spectral data of compounds 1−5 in CDCl3.

1 2 3 4 5
1 36.6 35.0 36.5 35.4 36.6
2 34.9 27.7 34.7 34.4 34.8
3 216.6 78.5 216.4 215.0 216.9
4 47.5 38.6 47.4 47.2 47.4
5 50.3 48.2 50.4 49.7 50.5
6 23.8 24.0 23.5 37.2 23.7
7 119.8 76.1 124.1 198.0 119.8
8 142.9 135.7 142.2 139.6 142.9
9 144.5 139.5 149.9 162.8 144.5
10 37.3 37.5 38.5 39.3 37.3
11 117.3 21.5 118.2 23.8 117.3
12 37.8 30.2 79.2 30.2 37.8
13 43.8 45.0 49.0 45.0 43.8
14 50.7 49.7 52.9 51.5 52.1
15 31.5 31.8 31.0 73.4 74.2
16 27.9 28.5 27.0 39.7 40.3
17 51.0 49.6 52.5 50.5 50.2
18 15.7 16.3 11.7 15.9 15.7
19 22.5 17.5 21.7 17.9 22.5
20 36.5 36.4 35.6 36.2 36.4
21 18.6 18.5 18.4 18.4 18.6
22 31.4 34.5 34.7 34.7 34.4
23 28.9 28.8 28.7 28.7 28.9
24 70.9 79.5 79.7 79.7 79.3
25 74.9 73.5 74.5 73.7 73.8
26 62.2 67.7 26.5 26.5 67.9
27 62.8 22.2 23.2 23.2 22.0
28 25.4 27.4 27.6 27.6 25.4
29 25.3 15.4 20.2 20.2 21.2
30 21.2 25.2 25.5 25.5 25.3
-OCH3 55.5 55.8