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. Author manuscript; available in PMC: 2012 Aug 26.
Published in final edited form as: Chem Biol. 2011 Aug 26;18(8):1021–1031. doi: 10.1016/j.chembiol.2011.07.015

Table 1.

1H and 13C NMR data for AD210a (5). 1H and 13C NMR data were recorded in DMSO-d6 (500 MHz for 1H and 125 MHz for 13C). Chemical shifts are reported in δ (ppm). Coupling constants are reported in Hz. Carbons are labeled according to their number in polyketide backbone.

AD210a (5)
no. 13C 1H Long-range 13C-1H HMBC correlations Long-range 1H -1H COSY correlations
1 160.5
2 88.1 5.13 (d, J = 1.7, 1H) C3, C4, C15 H4
3 170.2
4 100.7 5.56 (d, J = 1.7, 1H) C2, C3, C10, C20 H2
5 159.0
6 36.9 3.51 (s, 2H) C4, C7, C8, C11
7 136.9
8 119.1 6.21 (d, J = 1.8, 1H) C6, C10, C11 H10
9 160.5
10 100.1 6.08 (d, J = 1.8, 1H) C9, C12 H8
11 164.7
12 108.3
13 199.7
14 110.1
15 163.5
16 108.4 6.07 (d, J = 3.6, 1H) C15, C18, C21 H18
17 160.2
18 108.3 6.16 (d, J = 3.6, 1H) C8, C16, C17, C20 H16
19 144.7
20 33.1 2.19 (t, J = 6.5, 2H) C12, C19, C21 H21
21 31.4 1.21 (p, J = 5.9, 6.5, 2H) C20, C22, C23 H20, H22
22 30.3 1.14 (m, 2H) C20, C21, C23 H21, H23
23 21.8 1.04 (m, 2H) C21, C22, C24 H22, H24
24 13.9 0.78 (t, J = 5.75, 3H) C21, C22, C23 H23