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karl2100: ½ð±Ò+1, 3Q 2013-06-28 19:31:57
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karl2100: ½ð±Ò+1, 3Q 2013-06-28 19:31:57
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½20¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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