| ²é¿´: 214 | »Ø¸´: 1 | ||
zhangli1987Ìú³æ (СÓÐÃûÆø)
С½ð³æ
|
[ÇóÖú]
ÇóÖú΢Æ×²éѯ»¯ºÏÎï½á¹¹
|
| 19.28,19.51,19.75,20.49,23.58,25.26,30.88,32.04£¬41.84,43.10,43.94,44.37,49.15£¬50.06,50.45,50.95,63.31,65.07,65.31,116.15,149.19,165.86,214.98 |
» ²ÂÄãϲ»¶
»úе¹¤³Ì264ѧ˶Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
264Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
22408 266Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ43È˻ظ´
307Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
338Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
326·Ö£¬Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
[ÇóÖú] ÇóÖú΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Ò»Ö¬ÈÜÐÔ»¯ºÏÎïµÄ½á¹¹
ÒѾÓÐ9È˻ظ´
ÇóÖúÒ»»¯ºÏÎï΢Æ×½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
΢Æ×ÇóÖúÒ»»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»»¯ºÏÎï΢Æ×Êý¾Ý½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
ÇóÖú¡¡Î¢Æ×Êý¾Ý¿â £Ã£Î£Í£ÒÊý¾Ý²éδ֪»¯ºÏÎï½á¹¹
ÒѾÓÐ6È˻ظ´
ÇóÖúÈçϵÄÁ½¸ö»¯ºÏÎïÈçºÎͨ¹ýÆ×ͼÐÅÏ¢À´È·Ö¤¾ßÌåÊÇÄĸö½á¹¹£¿ лл
ÒѾÓÐ27È˻ظ´
¡¾ÇóÖú¡¿»¯ºÏÎï½á¹¹ÎÊÌâ
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿°ïæ½âÏ»¯ºÏÎïµÄ½á¹¹
ÒѾÓÐ16È˻ظ´

wangwang1989
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- Ó¦Öú: 525 (²©Ê¿)
- ½ð±Ò: 11769.2
- É¢½ð: 1451
- ºì»¨: 21
- ɳ·¢: 18
- Ìû×Ó: 4912
- ÔÚÏß: 315.2Сʱ
- ³æºÅ: 1467486
- ×¢²á: 2011-10-30
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhangli1987: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-06-17 21:10:10
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhangli1987: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-06-17 21:10:10
|
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£º¹²²éµ½41¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . longistylumphylline A C23H29NO3 ÏàËÆ¶È:65.2% Helvetica Chimica Acta 2005 Vol. 88 854 Longistylumphyllines A-C, Three New Alkaloids from Daphniphyllum longistylum Xin Chen, Zha-Jun Zhan, Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . paxiphylline E C23H29NO5 ÏàËÆ¶È:60.8% Helvetica Chimica Acta 2008 Vol. 91 2153 Three New Alkaloids, Paxiphyllines C¨C E, from Daphniphyllum paxianum Yu Zhang, Ying-Tong Di, Hai-Yang Liu, Chun-Shun Li, Cheng-Jian Tan, Qiang Zhang, Xin Fang, Shun-Lin Li, and Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . daphnilongeranin C C22H29NO3 ÏàËÆ¶È:56.5% Journal of Natural Products 2006 69(1) 79-82 Alkaloids from Daphniphyllum longeracemosum Sheng-Ping Yang, Hua Zhang, Chuan-Rui Zhang, Hua-Dong Cheng, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Daphlongamine F C23H29NO4 ÏàËÆ¶È:56.5% Helvetica Chimica Acta 2009 92 653-659 Alkaloids from the Leaves of Daphniphyllum longeracemosum Rosenth Chun-Shun Li, Ying-Tong Di, Qiang Zhang, Yu Zhang, Chen-Jian Tan, Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Prehelminthosporol C15H24O2 ÏàËÆ¶È:56.5% Journal of Natural Products 1988 Vol 51 821 Toxins from Weed Pathogens, I. Phytotoxins from a Bipolaris Pathogen of Johnson Grass L. M. Pena-Rodriguez, N. A. Armingeon, W. S. Chilton Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 3¦Â-Hydroxy-14-oxo-14,15-seco-5¦Â-card-20( 22)-enolide-15-nitrile C23H31NO4 ÏàËÆ¶È:56.5% Steroids 1996 61 572-582 Digitalis-like compounds: Synthesis and biological evaluation of seco-D and D-homo derivatives Mauro Gobbini, Alessandra Benicchio, Giuseppe Marazzi, Gloria Padoani, Marco T |

2Â¥2013-06-17 18:43:01














»Ø¸´´ËÂ¥