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. 2019 Feb 19;9:2248. doi: 10.1038/s41598-019-38696-3

Table 1.

1H (500 MHz) and 13C NMR (125 MHz) Data for 1–3 and 6 in DMSO-d6.

No 1 2 3
δC, type δH (J in Hz) δC, type δH (J in Hz) δC, type δH (J in Hz)
1 10.30, br s 10.43, br s 10.30, br s
2 176.2, C 175.3, C 177.9, C
3 74.9, C 76.2, C 72.3, C
3a 132.1, C 126.9, C 128.6, C
4 123.9, CH 7.16, d, 1 H (6.7) 124.1, CH 7.08, d, 1 H (7.5) 126.3, CH 7.04, d, 1 H (7.4)
5 121.4, CH 6.88, dd, 1 H (7.5, 7.5) 121.5, CH 6.90, dd, 1 H (7.5, 7.5) 120.9, CH 6.88, dd, 1 H (7.5, 7.5)
6 129.2, CH 7.18, dd, 1 H (7.7, 6.2) 130.1, CH 7.22, dd, 1 H (7.7, 7.7) 129.4, CH 7.13, dd, 1 H (7.5, 7.6)
7 109.4, CH 6.80, d, 1 H (7.6) 109.9, CH 6.78, d, 1 H (7.7) 109.2, CH 6.70, d, 1 H (7.5)
7a 143.0, C 142.6, C 142.3, C
8 117.5, CH 5.80, s, 1 H 41.7, CH2 2.57, s, 2 H
1′ 130.4, C 66.1, CH 4.40, s, 1 H 83.4, C
3′ 153.3, C 157.2, C 155.6, C
5′ 161.3, C 168.6, C 172.3, C
2′-NCH3 26.1, CH3 3.04, s, 3 H 31.3, CH3 3.14, s, 3 H 24.4, CH3 2.55, s, 3 H
4′-NCH3 24.4, CH3 2.83, s, 3 H 24.2, CH3 2.50, s, 3 H 23.7, CH3 2.19, s, 3 H
3-OH 6.85, s 6.62, s 6.70, s
1′-OH 6.00, s