| ²é¿´: 395 | »Ø¸´: 1 | |||
Ñà¿Ê¸ß·É½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
43--7΢Æ×ÇóÖú£¡£¡£¡Ð»Ð» ÒÑÓÐ1È˲ÎÓë
|
|
̼Æ×Êý¾Ý 8.77, 11.56, 12.61, 16.20, 21.25, 26.41, 27.18, 29.98, 36.46, 41.34, 43.35, 47.20, 70.91, 72.47, 74.09, 103.19, 129.04, 151.33, 170.31, 171.06, 175.52 |
» ²ÂÄãϲ»¶
272·Ö²ÄÁÏ×ÓÇóµ÷¼Á
ÒѾÓÐ36È˻ظ´
275Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
µ÷¼ÁÇóÊÕÁô
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
070300»¯Ñ§Ñ§Ë¶311·ÖÇóµ÷¼Á
ÒѾÓÐ19È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ13È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ33È˻ظ´
¸´ÊÔµ÷¼Á
ÒѾÓÐ7È˻ظ´
Ò»Ö¾Ô¸¹þ¹¤´ó 085600 277 12²Ä¿Æ»ùÇóµ÷¼Á
ÒѾÓÐ17È˻ظ´
»¹Óл¯¹¤¶þÂÖµ÷¼ÁµÄѧУÂð
ÒѾÓÐ47È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»df12
ÒѾÓÐ5È˻ظ´
΢Æ×Êý¾ÝÇóÖúлл
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬ÔÚÏßµÈ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ3¸ö»¯ºÏÎïµÄÄ£ºý²éÕÒ£¨¡·80%£©
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄάÆÕCÆ×Êý¾Ý~~~~ллÁË~~~~~
ÒѾÓÐ3È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ñà¿Ê¸ß·É: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-14 15:31:34
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ñà¿Ê¸ß·É: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-14 15:31:34
|
²éѯ½á¹û£º¹²²éµ½19¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (3¦Â,6¦Â,8¦Â,10¦Â)-3-acetyl-8,10-dihydroxy- 6-(2-methyl-1-oxo-butoxy)eremophil-7(10)-eno-12,8-lactone C22H32O8 ÏàËÆ¶È:95.4% Helvetica Chimica Acta 2009 92 495-501 New Eremophilane Sesquiterpenes from the Roots of Ligularia fischeri Meicai Deng, Weiwei Dong, Wei Jiao, Runhua Lu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 6¦Â-Acetoxy-3¦Â-angeloyloxy-8¦Â,10¦Â-dihydroxyeremophilenolide C22H30O8 ÏàËÆ¶È:77.2% Pharmazie 2005 60 313-316 Six new sesquiterpenes from Cacalia ainsliaeflora Man-Jun Mao, Biao Jiang, and Zhong-Jian Jia Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 6¦Â-(2'-methylbutanoyloxy)-3¦Â-acetoxy-8¦Â,10¦Â-dihydroxyeremophil-7(11)-en-8,12-olide C22H32O8 ÏàËÆ¶È:76.1% Planta Medica 2006 72 567-569 New Eremophilane-Type Sesquiterpenes from Ligularia hodgsonii Xu, Ji-Qing; Li, Yun-Sen; Li, Yi-Ming; Jiang, Shan-Hao; Tan, Chang-Heng; Zhu, Da-Yuan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 3¦Â-(2-methylbutyryloxy)-8¦Â,10¦Â-dihydroxy-6¦Â-methoxyeremophilenlide ÏàËÆ¶È:76.1% Chinese Chemical Letters 1998 9 65-68 Eremophilenolides from Cacalia Roborowskii Suo Ming ZHANG,Gui Ling ZHAO and Guo Qiang LIN Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 3¦Â-(2-Methylbutyroyloxy)-8¦Â,10¦Â-dihydroxy-6¦Â-methoxyeremophilenolide C21H32O7 ÏàËÆ¶È:76.1% Phytochemistry 1998 48 519-524 Eremophilane sesquiterpenes from Cacalia roborowskii Suoming Zhang, Guiling Zhao, Rong Li, Guoquiang Lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 3¦Â-acetoxy-10¦Â-hydroxy-6¦Â,8¦Â-dimethoxyeremophil-7(11)-en-12,8¦Á-olide C19H28O7 ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2008 Vol. 91 1118 New Sesquiterpenoids from Ligularia duciformis Wen-Shu Wang, Xia Dai, Li-Ya Hong, Peng Lu, Jin-Chao Feng, and Yu-Guo Jiao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 6¦Â-angeloyloxy-8¦Â,10¦Â-dihydroxy-3-oxoeremophilenolide C20H26O7 ÏàËÆ¶È:66.6% Planta Medica 2003 69 745-749 New Eremophilane Sesquiterpenes from Cacalia ainsliaeflora Manjun Mao,Zhongduo Yang,Zhongjian Jia Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 8¦Â,10¦Â-dihydroxy-6¦Â-isobutyryloxyeremophil-7(11)-en-(12,8)-olide C19H28O6 ÏàËÆ¶È:66.6% Tetrahedron 2008 64 4486-4495 Diversity of Ligularia kanaitzensis in sesquiterpenoid composition and neutral DNA sequences Motoo Tori, Aki Watanabe, Sachie Matsuo, Yasuko Okamoto, Kana Tachikawa, Shigeru Takaoka, Xun Gong, Chiaki Kuroda, Ryo Hanai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 3¦Â,6¦Â-Diangeloyloxy-8¦Â,10¦Â-dihydroxyeremophilenolide C25H34O8 ÏàËÆ¶È:64% Pharmazie 2005 60 313-316 Six new sesquiterpenes from Cacalia ainsliaeflora Man-Jun Mao, Biao Jiang, and Zhong-Jian Jia Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 3¦Â-angeloyloxy-6¦Â-ethoxy-8¦Â,10¦Â-di-hydroxyeremophilenolide C22H32O7 ÏàËÆ¶È:63.6% Planta Medica 2003 69 745-749 New Eremophilane Sesquiterpenes from Cacalia ainsliaeflora Manjun Mao,Zhongduo Yang,Zhongjian Jia Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 3¦Â-angeloyloxy-8¦Â,10b-dihydroxy-6¦Â-ethoxyeremophilenolied C22H32O7 ÏàËÆ¶È:63.6% Chinese Chemical Letters 2003 14 479-482 Two New Eremophilenolides from Cacalia ainsliaeflora Man Jun MAO, Cheng Shan YUAN, Chuan Zong ZOU, Zhong Jian JIA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 3¦Â-Acetoxy-6¦Â-(2-methylbutyryloxy)furanoeremophilan-10¦Â-ol C22H32O6 ÏàËÆ¶È:63.6% Natural Product Communications 2010 5 1-4 Two New Furanoeremophilane Sesquiterpenoids fromLigularia oligonema Hajime Nagano*, Mika Matsushima, Hiroka Yamada, Ryo Hanai,*, Xun Gong,* andChiaki Kuroda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 3¦Â-acetoxy-6¦Â,8¦Â,10¦Â-trihydroxyeremophil-7(11)-en-12,8¦Á-olide C17H24O7 ÏàËÆ¶È:61.9% Helvetica Chimica Acta 2008 Vol. 91 1118 New Sesquiterpenoids from Ligularia duciformis Wen-Shu Wang, Xia Dai, Li-Ya Hong, Peng Lu, Jin-Chao Feng, and Yu-Guo Jiao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 3¦Â-acetoxy-10¦Â-hydroxy-6¦Â,8¦Â-dimethoxyeremophil-7(11)-en-8¦Á,12-olide C19H28O7 ÏàËÆ¶È:61.9% Planta Medica 2009 75 635-640 Eremophilane-Type Sesquiterpene Derivatives from Ligularia hodgsonii Wen-Xian Li, Ming Lei, Dong-Qing Fei, Kun Gao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 3¦Â-acetoxyl-8¦Â,10¦Â-dihydroxy-6¦Â-methoxyeremophilenolide ÏàËÆ¶È:61.9% Chinese Chemical Letters 1998 9 65-68 Eremophilenolides from Cacalia Roborowskii Suo Ming ZHANG,Gui Ling ZHAO and Guo Qiang LIN Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 3¦Â-angeloyloxy-8¦Â,10¦Â-dihydroxy-6¦Â-methoxyeremophilenolide ÏàËÆ¶È:61.9% Chinese Chemical Letters 1998 9 65-68 Eremophilenolides from Cacalia Roborowskii Suo Ming ZHANG,Gui Ling ZHAO and Guo Qiang LIN Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 3¦Â-Acetoxyl-8¦Â,10¦Â-dihydroxy-6¦Â-methoxy eremophilenolide C18H26O7 ÏàËÆ¶È:61.9% Phytochemistry 1998 48 519-524 Eremophilane sesquiterpenes from Cacalia roborowskii Suoming Zhang, Guiling Zhao, Rong Li, Guoquiang Lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 3¦Â-angeloyloxy-8¦Â,10¦Â-dihydroxy-6¦Â-methoxyeremophilenolide C21H30O7 ÏàËÆ¶È:61.9% Phytochemistry 1998 48 519-524 Eremophilane sesquiterpenes from Cacalia roborowskii Suoming Zhang, Guiling Zhao, Rong Li, Guoquiang Lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . melanothyrsin C C20H28O7 ÏàËÆ¶È:61.9% Tetrahedron 2014 70 2621-2628 Twelve new compounds from Ligularia melanothyrsa; isolation of melanothyrsins A¨CE, normelanothyrsin A, and other eremophilane sesquiterpenoids Yoshinori Saito, Mayu Ichihara, Yasuko Okamoto, Xun Gong, Chiaki Kuroda, Motoo Tori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-04-14 12:30:28













»Ø¸´´ËÂ¥
10