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. Author manuscript; available in PMC: 2008 Nov 6.
Published in final edited form as: J Nat Prod. 2007 Feb 21;70(3):402–406. doi: 10.1021/np060592k

Table 1.

13C NMR and 1H NMR Data of Zorbamycin (1) [D2O, TSP, δ (ppm) (J = Hz)]a

positionb δC δH
1 173.8
2 55.2 4.07 mc
3 49.8 2.88–3.06 m
4 179.0
5 43.1 2.78 mc, 2.69 dd (15.0, 9.0)
6 62.5 4.05 mc
7 168.2
8 167.6
9 115.5
10 154.8
11 13.8 2.16 s
12 170.8
13 60.4 5.09 d (8.0)
14 75.6 5.28 d (8.0)
15 100.8 5.25 d (3.5)
16 66.0 4.20 mc
17 74.4 3.64 mc
18 70.9 4.12 mc
19 73.4 3.99 mc
20 101.3 5.02 brs
21 71.2 4.06 mc
22 77.1 4.65 mc
23 67.4 3.82 mc
24 76.5c 3.84 mc
25 63.8 3.80 mc, 3.94 mc
26 160.8
27 137.6
28 120.0 7.30 s
29 139.6 7.91 s
30 172.2
31 51.8 3.82 mc
32 34.5 1.70 m
33 76.5c 3.74 mc
34 45.2 2.36 m
35 14.3 1.07 d (7.0)
36 179.6
37 63.6 4.29 s
38 74.3
39 28.3d 1.19 s
40 174.2
41 40.1 3.58 mc
42 42.1 2.92 m
43 180.3
44 41.4 3.58 mc, 3.90 mc
45 78.4 5.89 dd (9.0, 7.0)
46 175.0
47 128.3 8.16 s
48 151.0
49 165.9
50 17.3 0.92 d (8.0)
51 61.4 3.50 mc
52 28.6d 1.22 s
53 39.4 3.81 mc
54 35.5 2.80 mc
55 171.8
a

Assignment confirmed by the combination of DEPT, 1H-1H COSY, TOCSY, HSQC, and HMBC, spectra obtained at 500 MHz for 1H and 125 MHz for 13C, respectively.

b

See Figure 2 for hydrogen and carbon numbering of ZBM.

c

Overlapped signals.

d

Interchangeable signals.