Research Article

Attenuated Structural Transformation of Aconitine during Sand Frying Process and Antiarrhythmic Effect of Its Converted Products

Table 4

1H (600 MHz) and13C (150 MHz) NMR data of compound 2.

Position2Aconitine
δH (J in Hz)δCHMBCNOESY1H–1H COSYδC

13.05 m83.6 dC-10, C-17, 1-OCH3H-3, H-10, 1-OCH3H-2α, β83.4 d
2α2.36 m34.1 tC-4——H-1, H-2β, H-334.1 t
2β2.17 mC-4, C-11——H-1, H-2α, H-3
33.67 m71.8 dC-18, C-19H-1, H-5H-2α, β70.4 d
4——43.7 s——————43.2 s
52.04 d (6.6)48.5 dC-3, C-7, C-10, C-17, C-18, C-19H-3, H-18α, βH-646.6 d
63.89 d (6.6)84.1 dC-4, C-8, C-17, 6-OCH3H-8, 6-OCH3H-5, H-782.3 d
72.78 m41.8 dC-9, C-11, C-156-OCH3H-6, H-844.8 d
82.65 m49.4 dC-10, C-15, C-17H-6, H-16H-7, H-992.0 s
92.80 m38.7 dC-12, C-13, C-15——H-8, H-10, H-1444.2 d
102.22 m44.8 dC-8, C-17H-1, H-14H-9, H-12α, β40.8 d
11——51.2 s——————49.8 s
12α3.02 m32.9 tC-11, C-13, C-14, C-16——H-10, H-12β36.2 t
12β1.83 mC-11, C-13, C-16H-14H-10, H-12α
13——77.5 s——————74.0 s
145.41 d (5.16)78.5 dC-8, C-13, C-16, ArC=OH-10, H-12βH-978.9 d
15——211.7 s——————78.9 d
163.85 s86.1 dC-12, C-15, 16-OCH3H-8, H-2′, 6′——90.1 d
172.98 s61.6 dC-1, C-6, C-10, C-19H-21——61.0 d
18α3.69 d (9.18)76.8 tC-3, C-5, C-19, 18-OCH3H-5, H-19α, β, 18-OCH3H-18β77.1 t
18β3.75 d (9.18)C-3, C-5, C-19, 18-OCH3H-5, H-19α, 18-OCH3H-18α
19α2.39 d (10.98)47.4 tC-3, C-5, C-18, C-21H-18α, βH-19β48.8 t
19β2.90 d (10.98)C-3, C-5, C-17H-18αH-19α
21α2.45 m49.0 tC-17, C-19H-17H-2246.9 t
21β2.52 mC-17, C-19H-17H-22
221.04 t (7.38)13.3 q————H-21α, β13.3 q
8-C=O——————————172.2 s
CH3——————————21.3 q
1-OCH33.24 s56.1 qC-1H-1——55.6 q
6-OCH33.24 s57.8 qC-6H-6, H-7——59.0 q
16-OCH33.80 s62.3 qC-16————60.7 q
18-OCH33.29 s59.2 qC-18H-18α, β——57.9 q
ArC=O——166.1 s——————165.9 s
1′——129.4 s——————129.8 s
2′, 6′7.97 d (7.32)129.7 dC-4′, ArC=OH-16H-3′, 5′129.6 d
3′, 5′7.46 t (7.32)128.6 dC-1′, ArC=O——H-2′, 6′, H-4′128.6 d
4′7.60 t (7.32)133.6 dC-2′, 6′H-3′, 5′H-3′, 5′133.2 d