| ²é¿´: 387 | »Ø¸´: 1 | |||
¼¾·çÔÂ½ð³æ (ÕýʽдÊÖ)
¿ÆÑвËÄñ
|
[ÇóÖú]
΢Æ×ÇóÖú£¬¸Ðл£¡ ÒÑÓÐ1È˲ÎÓë
|
|
CÆ×ÈçÏ£º 11.20,15.24,17.24,17.90,20.58,23.43,28.06,28.48,29.68,39.79,39.80,74.18,75.69,76.01,76.21,76.33,80.68,94.95,98.99,119.39,131.83,144.60,144.63,168.73,193.72 ÈܼÁÊÇë®´úÂȷ£¬ÁíÍâÔÚ-1.02´¦ÓзåÊÇÔõô»ØÊ£¿Çó½â£¡Ð»Ð»... |
» ²ÂÄãϲ»¶
Çóµ÷¼Á ²ÄÁÏÓ빤³Ì 324·Ö ר˶
ÒѾÓÐ3È˻ظ´
»¯Ñ§¹¤³ÌÓë¼¼Êõ324µ÷¼Á
ÒѾÓÐ15È˻ظ´
Ò»Ö¾Ô¸¿ó´ó£¬²ÄÁϹ¤³Ìר˶314·Ö£¬0856¿Éµ÷¶¼¿ÉÒÔ
ÒѾÓÐ12È˻ظ´
»·Ñõ¹à·â½º ¿¹³Á¼Á
ÒѾÓÐ4È˻ظ´
268·Ö085602»¯Ñ§¹¤³Ìµ÷¼Á
ÒѾÓÐ22È˻ظ´
¿¼Ñе÷¼Á
ÒѾÓÐ18È˻ظ´
»¹Óл¯¹¤¶þÂÖµ÷¼ÁµÄѧУÂð
ÒѾÓÐ39È˻ظ´
277 ÊýÒ»104£¬Ñ§Ë¶£¬Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
0854µ÷¼Á
ÒѾÓÐ5È˻ظ´
²ÄÁϹ¤³Ì302·ÖÇóµ÷¼Á
ÒѾÓÐ15È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
·Ç³£¸Ðл£¡Î¢Æ×ÇóÖú
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»~~
ÒѾÓÐ3È˻ظ´
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
Çó΢Æ×°ïæ,лл
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý3¸ö
ÒѾÓÐ6È˻ظ´
΢Æ× Ç󻯺ÏÎï
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
Çó΢Æ×¼ìË÷»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´

seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48426.9
- ºì»¨: 52
- Ìû×Ó: 6748
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¼¾·çÔÂ: ½ð±Ò+5, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-25 22:23:52
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¼¾·çÔÂ: ½ð±Ò+5, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-25 22:23:52
|
. euphohelioscopin A ÏàËÆ¶È:58.6% Journal of Chinese Medicinal Materials 2013 36 1092-1096 Study on Chemical Constituents of Euphorbia helioscopia and Their Antitumor Activities MU Shu-zhen, SHANG Shang, YAN Chen, YANG Fu-mei, HAO Xiao-jiang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 7-desacetoxy-9,10,13-tridesacetyl-9,10-O-isopropylidene baccatine VI C32H42O9 ÏàËÆ¶È:53.5% Tetrahedron 1997 53 12575-12594 Taxoïdes: 7-D¨¦shydroxy-10-ac¨¦tyldoc¨¦taxel et nouveaux analogues pr¨¦par¨¦s ¨¤ partir des alcaloïdes de l'If H¨¦l¨¨ne Poujol, Ali Al Mourabit, Alain Ahond, Christiane Poupat, Pierre Potier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . cynatratoside B (revised as cynatraoside B) C28H42O10 ÏàËÆ¶È:53.5% Journal of Chemical Research 2013 37 727-729 Two new pregnane glycosides from the roots of Cynanchum atratum Authors: Wang, Shilei; Shan, Weiguang; Ma, Liefeng; Zheng, Zhenzhen; Ying, Youmin; Zhan, Zhajun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . Garcihombronane F C30H46O4 ÏàËÆ¶È:50% Journal of Natural Products 2005 68 1222-1225 Friedolanostanes and Lanostanes from the Leaves of Garcinia hombroniana Vatcharin Rukachaisirikul, Somsak Saelim, Pueksa Karnsomchoke, and Souwalak Phongpaichit Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . Microtropioside A C26H44O9 ÏàËÆ¶È:50% Phytochemistry 2010 71 675-681 Microtropiosides A¨CF: ent-Labdane diterpenoid glucosides from the leaves of Microtropis japonica (Celastraceae) Yuka Koyama, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (24S)-1¦Â,3¦Â,24,25-tetrahydroxy-7,9(11)-euphadiene C30H48O3 ÏàËÆ¶È:50% Phytochemistry 2010 71 669-674 Euphane triterpenoids of Cassipourea lanceolata from the Madagascar rainforest Yanpeng Hou, Shugeng Cao, Peggy J. Brodie, James S. Miller, Chris Birkinshaw, Mamisoa N. Andrianjafy, Rabodo Andriantsiferana, Vincent E. Rasamison, Karen TenDyke, Yongchun Shen, Edward M. Suh, David G.I. Kingston Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . Cyclopside 2 C26H40O9 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry Letters 2014 24 3777-3781 Two new unusual monoterpene acid glycosides from Acacia cyclops with potential cytotoxic activity Amira Jelassi, Afifa Zardi-Bergaoui, Aymen Ben Nejma, Meriam Belaiba, Jalloul Bouajila, Hichem Ben Jannet Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-05-22 20:47:39













»Ø¸´´ËÂ¥