Skip to main content
. 2019 Jun 13;17(6):353. doi: 10.3390/md17060353

Table 1.

1H and 13C NMR data for kabirimine (2) in dimethyl sulfoxide (DMSO)-d6.

Position δC δH (J in Hz) COSY HMBC
1 42.1, CH2 3.77 brs (2H) 2
2 24.7, CH2 2.14 m; 1.62 m 1; -
3 25.3, CH 2.08 m 27
4 48.1, C -
5 172.5, C -
6 29.0, CH2 3.13 brd (11.2); 2.92 m 7; -
7 27.3, CH2 2.34 brt (11.2); 1.65 m 6; 8
8 72.5, CH 3.93 m
9 31.2, CH2 2.00 m; 1.43 brt (9.6) 8, 10; 8
10 39.0, CH2 1.75 m; 1.63 m 9; - 25; 25
11 80.6, C -
12 43.9, CH2 2.10 brd (13.3); 1.26 brdd (13.3, 9.7) 13; - 13, 14; 13, 14
13 53.7, CH 2.89 brd (9.7) 12, 14 12
14 61.5, CH 2.66 brd (8.1) 13, 15 15
15 76.0, CH 2.96 brd (8.1) 14 14, 16, 26
16 36.0, CH 1.99 m 26
17 33.3, CH2 1.98 m; 1.37 brt (12.5) 18; - 4; -
18 38.7, CH 3.06 brd (12.6) 17
19 129.4, CH 5.70 brs 4, 18, 21, 23
20 134.8, C -
21 20.7, CH2 2.24 m (2H) 22
22 35.6, CH2 2.07 m; 1.90 m 21; - 5; -
23 138.3, CH 6.42 dd (17.4, 10.9) 24 19, 21
24 112.1, CH2 5.13 d (17.4); 5.02 d (10.9) 23; 23 20; 20
25 23.7, CH3 1.19 s 10, 11, 12
26 10.5, CH3 1.05 brd (5.3) 16 15, 16, 17
27 17.7, CH3 0.96 d (6.6) 3 2, 3, 4