Research Article

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

Table 3

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

Position1Aconitine
δH (J in Hz)δCHMBCNOESY1H–1H COSYδC

13.06 m83.5 dC-10, C-17, 1-OCH3H-3, H-5, H-10, 1-OCH3H-2α, β83.4 d
2α2.32 m34.2 tC-4, C-11——H-1, H-2β, H-334.1 t
2β2.18 mC-4, C-11——H-1, H-2α, H-3
33.68 m71.5 dC-1, C-18, C-19H-1, H-5H-2α, β70.4 d
4——43.5 s——————43.2 s
52.03 d (6.6)48.1 dC-3, C-7, C-10, C-17, C-18, C-19H-1, H-3, H-18α, βH-646.6 d
63.92 d (6.6)84.1 dC-4, C-8, C-17, 6-OCH3H-8, 6-OCH3H-5, H-782.3 d
72.73 m42.5 dC-5, C-9, C-11, C-156-OCH3H-6, H-844.8 d
82.75 m48.5 dC-10, C-15, C-17H-6, H-2′, 6′H-7, H-992.0 s
92.78 m38.6 dC-12, C-13, C-15——H-8, H-10, H-1444.2 d
102.15 m43.1 dC-5, C-8, C-17H-1, H-14H-9, H-12α, β40.8 d
11——50.9 s——————49.8 s
12α2.71 m36.1 tC-9, C-11, C-13, C-14, C-16——H-10, H-12β36.2 t
12β2.26 mC-9, C-11, C-13, C-16H-14H-10, H-12α
13——76.5 s——————74.0 s
145.16 d (5.1)79.6 dC-8, C-13, C-16, ArC=OH-10, H-12βH-978.9 d
15——211.8 s——————78.9 d
163.29 s89.2 dC-8, C-12, C-14, C-15, 16-OCH3H-17, 16-OCH3——90.1 d
172.81 s61.9 dC-5, C-6, C-8, C-10, C-19H-16, H-21——61.0 d
18α3.68 d (9.18)76.2 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
19α2.37 d (10.98)47.4 tC-3, C-18, C-21H-18α, βH-19β48.8 t
19β2.89 d (10.98)C-3, C-5, C-17H-18αH-19α
21α2.41 m49.1 tC-17, C-19H-17H-2246.9 t
21β2.44 mC-17, C-19H-17H-22
221.01 t (7.32)13.3 q————H-21α, β13.3 q
8-C=O——————————172.2 s
CH3——————————21.3 q
1-OCH33.23 s56.1 qC-1H-1——55.6 q
6-OCH33.27 s57.9 qC-6H-6, H-7——59.0 q
16-OCH33.61 s61.7 qC-16H-16, H-2′, 6′——60.7 q
18-OCH33.28 s59.2 qC-18H-18α, ß——57.9 q
ArC=O——167.1 s——————165.9 s
1′——129.6 s——————129.8 s
2′, 6′7.94 d (7.32)129.8 dC-4′, ArC=OH-8, 16-OCH3H-3′, 5′129.6 d
3′, 5′7.40 t (7.32)128.4 dC-1′, ArC=O——H-2′, 6′, H-4′128.6 d
4′7.53 t (7.32)133.3 dC-2′, 6′H-3′, 5′H-3′, 5′133.2 d