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. 2018 Sep 12;16(9):330. doi: 10.3390/md16090330

Table 1.

13C (125 MHz) and 1H (500 MHz) NMR data of bagremycins F (1) and G (2) (in DMSO-d6).

No. 1 2
δC, Type δH (J in Hz) HMBC δC, Type δH (J in Hz) HMBC
1 126.5, C 118.1, C
2 113.1, C 121.9, CH 8.90, d (2.2) C3, C4, C6, C7
3 140.4, C 126.2, C
4 147.7, C 152.6, C
5 113.2, CH 6.78, d (8.2) C1, C3, C4 114.8, CH 6.99, d (8.5) C1, C4
6 119.1, CH 7.10, d (8.2) C2, C4, C7 126.9, CH 7.74, dd (8.5, 2.2) C2, C4, C7
7 165.7, C 164.3, C
8 150.5, C 150.4, C
9 122.0, CH 7.21, d (8.6) C8, C11, C13 122.1, CH 7.20, d (8.6) C8, C11, C13
10 127.1, CH 7.55, d (8.6) C8, C12, C14 127.1, CH 7.54, d (8.6) C8, C12, C14
11 134.7, C 134.7, C
12 127.1, CH 7.55, d (8.6) C8, C10, C14 127.1, CH 7.54, d (8.6) C8, C10, C14
13 122.0, CH 7.21, d (8.6) C8, C9, C11 122.1, CH 7.20, d (8.6) C8, C9, C11
14 135.8, CH 6.74, dd (17.7, 10.9) C10, C11, C12 135.8, CH 6.74, dd (17.6, 10.9) C10, C11, C12
15 114.3, CH2 5.29, dd (10.9, 0.6);
5.82, dd (17.7, 0.6)
C11, C14 114.3, CH2 5.27, dd (10.9, 0.7);
5.82, dd (17.6, 0.7)
C11, C14
16 35.5, CH2 2.98, dd (13.1, 8.4);
3.11, dd (13.1, 5.4)
C2, C17, C18 160.2, CH 8.33, d (1.6) C3
17 52.2, CH 4.25, m C18, C19
18 171.0, C
19 169.3, C
20 22.2, CH3 1.81, s C19
21 51.9, CH3 3.54, s C18
NH 8.41, d (7.5) C17, C19 9.78, s C3