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. 2013 Mar 15;18(3):3458–3466. doi: 10.3390/molecules18033458

Table 1.

1H and 13C-NMR data for compound 1 (400 and 100 MHz, in DMSO, ppm, J/Hz).

Positon δH δC HMBC
1 7.21 d (10.1) 156.9 C-3, C-5, C-9, C-10, C-19
2 6.11 dd (10.1, 1.9) 127.1 C-10
3 185.3
4 6.00 s 123.3 C-6, C-10
5 170.1
6 2.48 m2.33 m 32.4 C-5
7 2.27 m0.98 m 32.7
8 1.94 m 31.7
9 1.05 m 53.1 C-19
10 43.8
11 1.68 m1.61 m 22.3
12 1.57 m1.01 m 38.3 C-18
13 43.3
14 0.78 dd (11.1, 5.8) 59.0 C-8, C-13, C-18
15 4.10 m 69.0
16 2.18 m ( α ) 39.7 C-13
1.51 m ( β )
17 1.85 m 55.0
18 0.87 s 15.7 C-12, C-13, C-14, C-17
19 1.22 s 18.9 C-1, C-5, C-9, C-10
20 5.79 ddd(17.3, 10.4, 7.4) 139.6
21 4.98 dd (10.4, 1.7) 115.3 C-17
4.96 dd (17.3, 1.7)
15-OH 4.45 d (4.0)