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. 2017 Jul 19;5:e3601. doi: 10.7717/peerj.3601

Table 3. NMR data of actinomycin D (CDCl3, 1H: 500 MHz, 13C: 75.4 MHz).

α-ring Position δC δH β-ring Position δC δH
Thr 1 168.51 Thr 1 167.55
2 55.26 4.62 (dd) 2 54.90 4.52 (dd)
3 75.05 5.21 (qd) 3 74.98 5.18 (qd)
4 17.76 1.26 (3H, d) 4 17.34 1.25 (3H, d)
NH 7.16 (d) NH 7.76 (d)
D-Val 1 173.74 D-Val 1 173.32
2 58.90 3.56 (dd) 2 5873 3.53 (dd)
3 31.82 2.11 (m) 3 31.55 2.07 (m)
4 19.26 1.13 (3H, d) 4 19.08 1.12 (3H, d)
5 19.03 0.91 (3H, d) 5 18.98 0.89 (3H, d)
NH 8.15 (d) 8.01 (d)
Pro 1 173.37 Pro 1 173.32
2 56.44 6.03 (d) 2 56.26 5.96 (d)
3 31.29 1.89, 2.65 (m) 3 30.97 1.85, 2.65 (m)
4 23.00 2.15, 2.23 (m) 4 22.85 2.15, 2.23 (m)
5 47.59 3.74 (2H, dd) 5 47.33 3.84 (2H, m)
Sar 1 166.53 Sar 1 166.32
2 51.39 4.82, 3.64 (d) 2 51.39 4.71, 3.60 (d)
NMe 34.91 2.91 (3H, s) NMe 34.85 2.88 (3H, s)
MeVal 1 167.65 MeVal 1 166.53
2 71.45 2.68 (m) 2 71.28 2.68 (m)
3 26.92 2.68 (m) 3 26.92 2.68 (m)
4 21.66 0.96 (3H, d) 4 2,156 0.95 (3H, d)
5 19.21 0.75 (3H, d) 5 19.08 0.74 (3H, d)
NMe 39.27 2.94 (3H, s) NMe 39.14 2.88 (3H, s)
Chromophore
δH 2.56 (3H, s), 2.68 (3H, s), 7.37 (d), 7.64 (d)
δC 7.74, 15.00, 101.75, 113.52, 125.80, 127.59, 129.13, 130.25, 132.65, 140.50, 145.12, 145.90, 147.64, 166.53, 168.99, 179.12