| ²é¿´: 185 | »Ø¸´: 1 | |||
hejiangboľ³æ (ÖøÃûдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý²éѯ
|
|
ÏàËÆ¶È£º50% ÈܼÁ£ºÂÈ·Â ºË´ÅÊý¾Ý£º16.0,18.0,19.5,20.6,25.3,28.8,29.1,29.7,36.9,38.9,54.0,57.3,71.9,73,3,80.9,127.4,139.5,141.8,144.4,168.4 |
» ²ÂÄãϲ»¶
µ÷¼ÁÇóÊÕÁô
ÒѾÓÐ6È˻ظ´
272·Ö²ÄÁÏ×ÓÇóµ÷¼Á
ÒѾÓÐ36È˻ظ´
275Çóµ÷¼Á
ÒѾÓÐ8È˻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´

ľ·ç·ãpan
ľ³æ (СÓÐÃûÆø)
- Ó¦Öú: 134 (¸ßÖÐÉú)
- ½ð±Ò: 1907.2
- ºì»¨: 4
- Ìû×Ó: 255
- ÔÚÏß: 73.5Сʱ
- ³æºÅ: 2011576
- ×¢²á: 2012-09-18
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hejiangbo: ½ð±Ò+15, XIEXIE 2012-11-17 13:49:27
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hejiangbo: ½ð±Ò+15, XIEXIE 2012-11-17 13:49:27
|
1 . 3¦Â-angeloyloxy-4¦Á,11-dihydroxy-6,7-dehydroeudesman-8-one ÏàËÆ¶È:90.4% Phytochemistry 1996 43 417-421 Eudesmane derivatives from Pluchea quitoc Giselle M. S. P. Guilhon, Adolfo H. M¨¹ller Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . compound2 ÏàËÆ¶È:76.1% Phytochemistry 1996 43 417-421 Eudesmane derivatives from Pluchea quitoc Giselle M. S. P. Guilhon, Adolfo H. M¨¹ller Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 4¦Â-acetoxy-3¦Â-angeloyloxy-11-hydroxy-6,7-dehydroeudesman-8-one ÏàËÆ¶È:63.6% Phytochemistry 1996 43 417-421 Eudesmane derivatives from Pluchea quitoc Giselle M. S. P. Guilhon, Adolfo H. M¨¹ller Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . arguticinin C22H32O7 ÏàËÆ¶È:63.6% Phytochemistry 1988 27 1861-1862 Arguticinin,a sesquiterpene from Pluchea arguta Viqar Uddin Ahmad,Kaniz Fizza Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 3¦Â-hydroxy-5¦Á-angeloyloxysilphinene C20H28O2 ÏàËÆ¶È:61.9% Journal of Natural Products 2002 65 448-453 C-5-Substituted Antifeedant Silphinene Sesquiterpenes from Senecio palmensis Mat¨ªas Reina, Matthias Nold, Omar Santana,Juan Carlos Orihuela, and Azucena Gonz¨¢lez-Coloma Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 3¦Â-angeloyloxy-4¦Â-hydroxy-7¦Á-H-eudesman-8-one ÏàËÆ¶È:61.9% Phytochemistry 1998 47 227-229 Eudesmane sesquiterpenoids from Pluchea quitoc Giselle M. S. P. Guilhon, Adolfo H. M¨¹ller Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . pluchecin C20H30O6 ÏàËÆ¶È:61.9% Phytochemistry 1991 30 689-691 Sesquiterpenes from Pluchea arguta Viqar Uddin Ahmad, Kaniz Fizza, Mohammad Aslam Khan, Tanveer Ahmed Farooqui Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . sclerotiotide G C23H36N4O6 ÏàËÆ¶È:60.8% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . sclerotiotide H C23H38N4O6 ÏàËÆ¶È:60.8% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . sclerotiotide J C23H38N4O6 ÏàËÆ¶È:60.8% Journal of Natural Products 2010 73 1133-1137 Cyclic Tripeptides from the Halotolerant Fungus Aspergillus sclerotiorum PT06-1 Jinkai Zheng, Zhihong Xu, Yi Wang, Kui Hong, Peipei Liu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2012-11-17 13:37:00













»Ø¸´´ËÂ¥