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. Author manuscript; available in PMC: 2010 Nov 25.
Published in final edited form as: Chem Biol. 2009 Nov 25;16(11):1197–1207. doi: 10.1016/j.chembiol.2009.11.005

Table 3.

1H and 13C NMR data for AD211a (8) and AD281a (19).

AD211a (8)
AD281a (19)
no. 13C 1H 13C 1H


1 159.2 160.7
2 89.6 5.37 (d, J=1.7, 1H) 88.3 5.14 (d, J=1.7, 1H)
3 169.8 170.2
4 108.7 6.03 (d, J=1.7) 100.5 5.56 (d, J=1.7, 1H)
5 154.2 159.1
6 48.5 4.16 (s, 2H) 47.2 3.5 (s, 2H)
7 134.7 136.9
8 109.1 6.76 (d, J=6.8, 1H) 119.4 6.21 (d, J=1.8, 1H)
9 128.7 7.28 (dd, J=6.8,7.1, 1H) 160.5
10 116.6 6.94 (d, J=7.1, 1H) 99.6 6.08 (d, J=1.8, 1H)
11 157 164.7
12 119.5 108.3
13 202.9 199.7
14 119.5 110.1
15 134.6 163.5
16 105.1 6.06 (d, J=1.6, 1H) 102.9 6.06 (d, J=3.6, 1H)
17 163.9 160.2
18 100.2 6.17 (d, J=1.6, 1H) 100.3 6.15 (d, J=3.6, 1H)
19 160.4 144.7
20 102.8 36.8 2.18 (t, 2H)
21 155.3 30.9 1.2 (m, 2H)
22 113.2 6.63 (s,1H) 27.7 1.2 (m, 1H)
23, 23’ 138 22.2 0.79 (d, J=0.54, 6H)
24 19.9 1.95 (s, 3H)

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.