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21.92,27.72,29.68,36.16,38.07,40.09,41.88,43.16,43.87,50.43,50.50,56.47,57.43,58.82,59.20,62.22,63.89,74.43,75.97,77.98,78.59,81.13,81.39,82.61,92.90,128.53,129.72,133.22,166.15
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1 .     neoline
    ÏàËÆ¶È:86.2%
Natural Product Research and Development          2003          15          324-325,340
CHEMICAL CONSTITUENTS FROM ACONITUM CARMICHAELI
CHEN Hong-chao; WANG Xian-kai; ZHAO Tong-fang; LIAO Xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Hokbusine A
C32H45NO10     ÏàËÆ¶È:76.6%
Journal of Natural Products          1989          Vol 52          720
Methanolysis of the C-8 Acetoxyl Group in Aconitine-Type Alkaloids: A Partial Synthesis of Hokbusine A
Haridutt K. Desai, Balawant S. Joshi, Samir A. Ross, S. William Pelletier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     hypaconitine
    ÏàËÆ¶È:74.1%
Natural Product Research and Development          2008          20          440-443
Diterpenoid Alkaloids from the Processed Roots of Aconitum carmichaeli
XIONG Jiang; GU Kun; TAN Ning-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (-)-(A-b)-14¦Á-Benzoyloxy-N-ethyl-8¦Â,13¦Â,15¦Á-trihydroxy-1¦Á,16¦Â,18-trimethoxyaconitane
C31H43NO8     ÏàËÆ¶È:74.1%
Journal of Natural Products          2012          75          1145-1159
Diterpenoid Alkaloids from the Lateral Root of Aconitum carmichaelii
Bingya Jiang, Sheng Lin, Chenggen Zhu, Sujuan Wang, Yanan Wang, Minghua Chen, Jianjun Zhang, Jinfeng Hu, Naihong Chen, Yongchun Yang, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     8-methoxy 14-benzoylhypaconine
    ÏàËÆ¶È:73.3%
Korean Journal of Pharmacognosy          1994          25(4)          395-398
Diterpene Alkaloid from Aconitum napiforme
Kim, Young-Ho; Hwang, Bang-Yeon; Kim, Hang-Sub; Lee, Sung-Woo; Lee, Hyeong-Kyu; Lee, Jung-Joon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     hypaconitine
    ÏàËÆ¶È:72.4%
Acta Pharmaceutica Sinica          1999          Vol 34          873-876
ISOLATION AND IDENTIFICATION OF TRIESTER DIDERPENOID FROM THE FLOWERS OF ACONITUM KUSNEZOFFII REICHB
Ren Yulin(Ren YL); Huang Zhaohong(Huang ZH) and Jia Shishan(Jia SS)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3-O-acetylhokbusine A
C34H47NO11     ÏàËÆ¶È:71.8%
Journal of Natural Products          1989          Vol 52          720
Methanolysis of the C-8 Acetoxyl Group in Aconitine-Type Alkaloids: A Partial Synthesis of Hokbusine A
Haridutt K. Desai, Balawant S. Joshi, Samir A. Ross, S. William Pelletier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (-)-(A-b)-14¦Á-Benzoyloxy-N-ethyl-8¦Â,13¦Â-dihydroxy-1¦Á,6¦Á,16¦Â,18-tetramethoxyaconitane
C32H45NO8     ÏàËÆ¶È:71.8%
Journal of Natural Products          2012          75          1145-1159
Diterpenoid Alkaloids from the Lateral Root of Aconitum carmichaelii
Bingya Jiang, Sheng Lin, Chenggen Zhu, Sujuan Wang, Yanan Wang, Minghua Chen, Jianjun Zhang, Jinfeng Hu, Naihong Chen, Yongchun Yang, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (-)-(A-b)-14¦Á-Benzoyloxy-N-ethyl-6¦Á,15¦Á-dihydroxy-1¦Á,8¦Â,16¦Â,18-tetramethoxyaconitane
C32H45NO8     ÏàËÆ¶È:71.8%
Journal of Natural Products          2012          75          1145-1159
Diterpenoid Alkaloids from the Lateral Root of Aconitum carmichaelii
Bingya Jiang, Sheng Lin, Chenggen Zhu, Sujuan Wang, Yanan Wang, Minghua Chen, Jianjun Zhang, Jinfeng Hu, Naihong Chen, Yongchun Yang, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     8-O-etthyl-14-benzoylmesaconine
C33H47NO11     ÏàËÆ¶È:70.9%
Chemical & Pharmaceutical Bulletin          1985          33          4717-4722
Studies on the Constituents of Aconitum Species. IV. On the Components of Aconitum japonicum THUNB.
HIDEO BANDO,KOJI WADA,MASAKI WATANABE,TAKAO MORI and TAKASHI AMIYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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