| ²é¿´: 290 | »Ø¸´: 1 | ||
zhiwu1983ľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý
|
| ̼Æ×Êý¾ÝÈçÏ£º19.1,20.3,21.0,21.1,23.3,28.0,28.1,29.8,41.5,41.8,43.1,43.5,45.1,50.7,51.5,57.1,62.4,63.1,69.1,69.5,72.1,73.9,102.3,110.4,121.9,140.4,143.5,169.2,170.1,210.3,219.8 |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
070300»¯Ñ§Ñ§Ë¶311·ÖÇóµ÷¼Á
ÒѾÓÐ15È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ13È˻ظ´
²ÄÁÏÓ뻯¹¤×¨Ë¶306·ÖÕÒºÏÊʵ÷¼Á
ÒѾÓÐ19È˻ظ´
»¯Ñ§¹¤³Ìµ÷¼Á289
ÒѾÓÐ19È˻ظ´
»¯¹¤Ñ§Ë¶ 285Çóµ÷¼Á
ÒѾÓÐ22È˻ظ´
298Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
368»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
326Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú STR½á¹ûµÄ TRFLP Êý¾Ý·ÖÎö
ÒѾÓÐ16È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬¸ø30J
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý YC-8
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý ÖØ½±
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´

jasminelw
Ìú¸Ëľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 269 (´óѧÉú)
- ½ð±Ò: 8813.7
- É¢½ð: 80
- ºì»¨: 6
- Ìû×Ó: 972
- ÔÚÏß: 604.2Сʱ
- ³æºÅ: 1858727
- ×¢²á: 2012-06-13
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhiwu1983: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-09-18 13:33:14
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhiwu1983: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-09-18 13:33:14
|
²éѯ½á¹û£º¹²²éµ½12240¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 12-dehydro-29-exo-neoazedarachin D C29H38O9 ÏàËÆ¶È:83.8% Phytochemistry 2013 89 59-70 Limonoids from the fruits of Melia azedarach and their cytotoxic activities Toshihiro Akihisa, Xin Pan, Yasuhiro Nakamura, Takashi Kikuchi, Nami Takahashi, Masahiro Matsumoto, Eri Ogihara, Makoto Fukatsu, Kazuo Koike, Harukuni Tokuda Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 12-dehydroneoazedarachin D C29H38O9 ÏàËÆ¶È:80.6% Phytochemistry 2013 89 59-70 Limonoids from the fruits of Melia azedarach and their cytotoxic activities Toshihiro Akihisa, Xin Pan, Yasuhiro Nakamura, Takashi Kikuchi, Nami Takahashi, Masahiro Matsumoto, Eri Ogihara, Makoto Fukatsu, Kazuo Koike, Harukuni Tokuda Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Meliatoxin B1 ÏàËÆ¶È:80% Bioorganic & Medicinal Chemistry 1996 4 1355-1359 Cytotoxic trichilin-type limonoids from Melia azedarach Koichi Takeya, Zhi-Sheng Qiao, Chieko Hirobe, Hideji Itokawa Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Meliarachin K C31H40O11 ÏàËÆ¶È:77.4% Helvetica Chimica Acta 2011 Vol. 94 1515-1526 Meliarachins A¨CK: Eleven Limonoids from the Twigs and Leaves of Melia azedarach Zu-Shang Su, Sheng-Ping Yang, Sheng Zhang, Lei Dong, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Meliatoosenin G C31H40O11 ÏàËÆ¶È:77.4% Phytochemistry 2012 73 106-113 Limonoids from the fruits of Melia toosendan Yi Zhang, Chun-Ping Tang, Chang-Qiang Ke, Xi-Qiang Li, Hua Xie, Yang Ye Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 1¦Á,11¦Â-diacetoxy-4¦Á-carbomethoxy-7¦Á-hydroxy-12¦Á-(2-methylpropanoyloxy)-15-oxohavanensin C35H48O12 ÏàËÆ¶È:76.4% Journal of Agricultural and Food Chemistry 2004 52 5027-5031 New Mosquito Larvicidal Tetranortriterpenoids from Turraea wakefieldii and Turraea floribunda Mary W. Ndung'u, Bakari Kaoneka, Ahmed Hassanali, Wilber Lwande, Antony M. Hooper, Francis Tayman, Oliver Zerbe, and Baldwyn Torto Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . sendanlin ÏàËÆ¶È:75% Bulletin of the Chemical Society of Japan 1994 67 2468-2472 The Structures of Azedarachins, Limonoid Antifeedants from Chinese Melia azedarach Linn Ruo Chun Huang, Hiroaki Okamura, Tetsuo Iwagawa, Munehiro Nakatani Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Trichilin D C35H46O12 ÏàËÆ¶È:74.2% Phytochemistry 1994 36 39-41 Limonoid antifeedants from chinese Melia azedarach Munehiro Nakatani, Ruo Chun Huang, Hiroaki Okamura, Hideo Naoki, Tetsuo Iwagawa Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . trichilin D C35H46O12 ÏàËÆ¶È:74.2% Bulletin of the Chemical Society of Japan 1994 67 2468-2472 The Structures of Azedarachins, Limonoid Antifeedants from Chinese Melia azedarach Linn Ruo Chun Huang, Hiroaki Okamura, Tetsuo Iwagawa, Munehiro Nakatani Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . musiduol C30H38O10 ÏàËÆ¶È:74.1% Journal of Natural Products 2006 69 975-977 Musidunin and Musiduol, Insect Antifeedants from Croton jatrophoides Ken-ichi Nihei, Yukihiro Asaka, Yoshihiro Mine, Yoichi Yamada, Masayuki Iigo, Tadashi Yanagisawa, and Isao Kubo Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Mesendanin D C30H42O7 ÏàËÆ¶È:74.1% Journal of Natural Products 2010 73 1344-1349 Mesendanins A−J, Limonoids from the Leaves and Twigs of Melia toosendan Shi-Hui Dong, Chuan-Rui Zhang, Xiu-Feng He, Hong-Bing Liu, Yan Wu and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . mesendanin L C28H38O8 ÏàËÆ¶È:74.1% Planta Medica 2013 79 163-168 Cytotoxic Limonoids from Melia azedarach Yuan, Chun-Mao; Zhang, Yu; Tang, Gui-Hua; Li, Yan; He, Hong-Ping; Li, Shi-Fei; Hou, Li; Li, Xing-Yao; Di, Ying-Tong; Li, Shun-Lin; Hua, Hui-Ming; Hao, Xiao-Jiang: Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 1,3-epi-29-[(2-methylbutanoyl)oxy]-2¦Á-hydroxyamoorastatone C33H44O11 ÏàËÆ¶È:72.7% Helvetica Chimica Acta 2009 92 1191-1197 Three New Limonoids from Melia toosendan Chun-Yan Zhou, Hai-Ying Tang, Xiang Li, Yi-Shu Sang Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 1,3-epi-29-[(2-methylpropanoyl)oxy]-2¦Á-hydroxyamoorastatone C32H42O11 ÏàËÆ¶È:71.8% Helvetica Chimica Acta 2009 92 1191-1197 Three New Limonoids from Melia toosendan Chun-Yan Zhou, Hai-Ying Tang, Xiang Li, Yi-Shu Sang Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . Mesendanin C C32H44O9 ÏàËÆ¶È:71.8% Journal of Natural Products 2010 73 1344-1349 Mesendanins A−J, Limonoids from the Leaves and Twigs of Melia toosendan Shi-Hui Dong, Chuan-Rui Zhang, Xiu-Feng He, Hong-Bing Liu, Yan Wu and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (3¦Â,5¦Á)-20-hydroxy-6-oxocevan-3-yl acetate C29H45NO4 ÏàËÆ¶È:70.9% Chemistry & Biodiversity 2008 Vol. 5 259 Cytotoxic Alkaloids from the Bulbs of Fritillaria hupehensis Yong-Hui Zhang, Xi-Liang Yang, Peng Zhang, Xue-Feng Zhou, Han-Li Ruan, Hui-Fang Pi, Ji-Zhou Wu, and Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 11¦Â-hydroxycneorin G C30H38O11 ÏàËÆ¶È:70.9% Phytochemistry 2004 65 3075-3081 Limonoids from Cedrela sinensis Kumiko Mitsui, Masato Maejima, Haruhiko Fukaya,Yukio Hitotsuyanagi, Koichi Takeya Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 20-epi-20-O-deacetyl-20-methoxyteupyreinidin C27H36O10 ÏàËÆ¶È:70.9% Journal of Natural Products 2002 65 142-146 Neoclerodane Diterpenoids from Teucrium montbretii Subsp. libanoticum and Their Absolute Configuration Maurizio Bruno, Maria Luisa Bond¨ª, Sergio Rosselli, Antonella Maggio, Franco Piozzi, and Nelly A. Arnold Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 13-acetyl-9-deoxyglanduline C29H39NO8 ÏàËÆ¶È:70.9% Chemistry of Natural Compounds 2000 36 419-477 HETISANE-TYPE DITERPENOID ALKALOIDS I. A. Bessonova and Sh. A. Saidkhodzhaeva Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 11,13-diacetyl-9-deoxyglanduline C31H41NO9 ÏàËÆ¶È:70.9% Chemistry of Natural Compounds 2000 36 419-477 HETISANE-TYPE DITERPENOID ALKALOIDS I. A. Bessonova and Sh. A. Saidkhodzhaeva Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-09-18 13:29:58














»Ø¸´´ËÂ¥