Table 4.
NMR data of aplysinin B (3) (600 MHz, DMSO-d6) and compound 21.
| position | 3 | 21a | ||
| δC | δH | δC | ||
| 1 | 134.9, C | – | 136.36 | |
| 2, 6 | 131.7, CH | 7.88, 2H, s | 132.98 | |
| 3, 5 | 118.5, C | – | 119.48 | |
| 4 | 154.4, C | – | 154.46 | |
| 7 | 135.7, CH | 7.33, d (15.8) | 138.42 | |
| 8 | 124.9, CH | 6.66, d (15.8) | 123.95 | |
| 9 | 165.0, C | – | 167.50 | |
| 10 | 38.4, CH2 | 3.20, 2H, m | 39.27 | |
| 11 | 28.1, CH2 | 1.71, 2H, m | 25.92 | |
| 12 | 22.0, CH2 | 2.45, 2H, m | 125.89 | |
| 13 | 126.8, C | – | 110.87 | |
| 14 | 109.2, CH | 6.60, s | 146.43 | |
| 15 | 147.4, C | – | – | |
| 4-OMe | 61.0, CH3 | 3.82, s | 61.26 | |
| 9-NH | – | 8.17, t (5.58) | – | |
aThe 13C NMR data were obtained in CD3OD [38].