| ²é¿´: 210 | »Ø¸´: 1 | ||
·çÖ®»êÁézdľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖúάÆÕÊý¾Ý
|
|
10.85,16.33,17.52,17.92,18.65,29.33,29.42,29.79,30.31,30.45,30.92,31.55,31.72,31.95,33.39,36.15,36.65,37.15,39.35,40.35,44.38,49.78,54.89,56.08,77.35,146.72,193.45,195.02 CDCl3 |
» ²ÂÄãϲ»¶
307·Ö²ÄÁÏרҵÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
336Çóµ÷¼Á£¬Ò»Ö¾Ô¸Öпƴó
ÒѾÓÐ9È˻ظ´
Çóµ÷¼Á Ò»Ö¾Ô¸Î÷ÄϽ»Í¨´óѧ085701»·¾³¹¤³Ì 282·Ö
ÒѾÓÐ15È˻ظ´
»¯Ñ§¹¤³Ìµ÷¼Á289
ÒѾÓÐ24È˻ظ´
284Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
275 Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
²ÄÁϹ¤³Ì322
ÒѾÓÐ16È˻ظ´
»¯¹¤Ñ§Ë¶ 285Çóµ÷¼Á
ÒѾÓÐ24È˻ظ´
293µ÷¼Á
ÒѾÓÐ18È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÌìȻҩÎﻯѧ°æ¿ì³ÉΪ¡°Î¬ÆÕ¡±ÇóÖú°æÁË£¬¿ª±Ù¸ö¡°Î¬ÆÕ¡±Êý¾ÝÇóÖú×Ó°æÈçºÎ£¿
ÒѾÓÐ19È˻ظ´
ÇóÖúάÆÕÊý¾Ý¿âÎÄÏ×һƪ
ÒѾÓÐ1È˻ظ´
ÒÒõ£±ûͪµÄÉú²ú¹¤ÒÕÉè¼Æ
ÒѾÓÐ7È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïάÆÕÊý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïάÆÕÊý¾Ý
ÒѾÓÐ6È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄάÆÕCÆ×Êý¾Ý~~~~ллÁË~~~~~
ÒѾÓÐ3È˻ظ´
ÇóÖú ²éѯάÆÕÊý¾Ý¡£¡£¡£¡£¡£¼±¼±¼± ÔÚÏߵȡ£¡£¡£¡£¡£×·¼Ó½ð±Ò¡£¡£¡£
ÒѾÓÐ10È˻ظ´
ÇóÖú£º±¾ÈËÐèÒªÍê³ÉÒ»·ÝËÎÛȾ¿ØÖƹ¤³ÌµÄÂÛÎÄ£¬²»ÖªµÀдʲô£¬Çó¸÷λָµã¡£
ÒѾÓÐ16È˻ظ´
ÈçºÎ´ò¿ª¿ÆÑÐ˼·
ÒѾÓÐ4È˻ظ´
²ËÄñÇóÖú£¬¼ª°²ºóºÓµ÷²éÉêÇëÊéÖÐÁ¢ÏîÒÀ¾ÝºÍ¿ÉÐÐÐÔ·ÖÎöÈçºÎд£¿
ÒѾÓÐ19È˻ظ´
ÇóÖúάÆÕÕ˺ÅÃÜÂë
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿ÇëÎÊÒ»°ãÔÚÄĸöÊý¾Ý¿â²éרÀûÈ«ÎÄ
ÒѾÓÐ11È˻ظ´
½Ì½ÌÎÒÈçºÎʹÓÃάÆÕ
ÒѾÓÐ8È˻ظ´
¡¾Ëزġ¿¿ÆÑбر¸ÖªÊ¶ÓëÈí¼þ
ÒѾÓÐ19È˻ظ´
¡¾ÌÖÂÛ¡¿ÇóÖú£º£ºNOTEEXPRESS Ö±½ÓÁ¬ÏßάÆÕÊý¾Ý¿âÏÂÔØÈ«ÎÄ
ÒѾÓÐ3È˻ظ´
¡¾ÇóÖú¡¿¹ØÓÚÓÃάÆÕÊý¾Ý¿âµÄ²é×ÊÁϵÄÎÊÌâ
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿ÂÈ»¯ÑÇí¿
ÒѾÓÐ14È˻ظ´

liuchao555
ľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 50 (СѧÉú)
- ½ð±Ò: 9559.9
- É¢½ð: 379
- ºì»¨: 2
- Ìû×Ó: 1605
- ÔÚÏß: 192.6Сʱ
- ³æºÅ: 872647
- ×¢²á: 2009-10-14
- ÐÔ±ð: GG
- רҵ: ÔªËØ»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
PSA: ½ð±Ò+1, лл 2013-04-25 17:18:02
·çÖ®»êÁézd: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-04-25 18:53:46
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
PSA: ½ð±Ò+1, лл 2013-04-25 17:18:02
·çÖ®»êÁézd: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-04-25 18:53:46
|
D: A-friedoolean-24-al-3-en-3-ol-2-one-29-oic acid ÏàËÆ¶È:86.6% Phytochemistry 1997 45 969-974 Triterpenoid inhibitors of interleukin-1 secretion and tumour-promotion from Tripterygium wilfordii var. regelii Yoshihisa Takaishi, Noriko Wariishi, Hideo Tateishi, Kazuyoshi Kawazoe, Kimiko Nakano, Yukihisa Ono, Haruyuki Tokuda, Hoyoku Nishino, Akio Iwashima Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . cangoronine C30H44O5 ÏàËÆ¶È:86.6% Acta Pharmaceutica Sinica 1999 Vol 34 210-213 THE TRITERPENOIDS OF TRIPTERYGIUM WILFORDII Guo Fujiang (Guo FJ); Fang Peifen (Fang Pf) and Li Yuanchao (Li YC) Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . cangoronine ÏàËÆ¶È:86.6% Phytochemistry 1995 39 1153-1157 Triterpenes from Tripterigium wilfordii Takashi Morota, Chun-Xin Yang, Hiroshi Sasaki, Wan-Zhang Qin, Kô Sugama, Kang-Li Miao, Takaaki Yoshino, Li-Hong Xu, Masao Maruno, Bing-Hui Yang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . cangoronine C30H40O5 ÏàËÆ¶È:86.6% Phytochemistry 1991 30 3713-3716 Triterpenes fromMaytenus ilicifolia Hideji Itokawa, Osamu Shirota, Hiroshi Ikuta, Hiroshi Morita, Koichi Takeya, Yoichi Iitaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . cangoronine C30H44O5 ÏàËÆ¶È:86.6% Chinese Pharmaceutical Journal 2000 35 50-51 Studies on triterpenoids in total glucosides of Tripterygium wilfordii Yang Guangzhong (Yang GZ), Guo Fujiang (Guo FJ), Li Yuanchao (Li YC Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . salacenonal ÏàËÆ¶È:79.3% Phytochemistry 1996 42 1377-1385 Biogenetically important quinonemethides and other triterpenoid constituents of Salacia reticulata Bhavani Dhanabalasingham, Veranja Karunaratne, Yasuhiro Tezuka, Tohru Kikuchi, A. A. Leslie Gunatilaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 3-hydroxy-D:A-friedoolean-3-en-2-on-29-oic acid ÏàËÆ¶È:73.3% Phytochemistry 1995 39 1153-1157 Triterpenes from Tripterigium wilfordii Takashi Morota, Chun-Xin Yang, Hiroshi Sasaki, Wan-Zhang Qin, Kô Sugama, Kang-Li Miao, Takaaki Yoshino, Li-Hong Xu, Masao Maruno, Bing-Hui Yang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 3-hydroxy-2-oxo-3-fridelen-20¦Á-carboxylic acid C30H46O4 ÏàËÆ¶È:73.3% Chinese Journal of Natural Medicines 2004 2 208-210 Studies on the Chemical Constituent of Tripterygium wilfordill Hook .F PENG Xiao-Yun; YANG Pei-Ming Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 3-hydroxy-2-oxo-3-fridelen-20¦Á-carboxylic acid C30H46O4 ÏàËÆ¶È:73.3% Natural Product Research and Development 2000 12(4) 1-7 STUDIES ON TRITERPENOIDS CONSTITUENTS OF TRIPTERYGIUM WILFORDII HOOK.F. Miao Kangli; Zhang Xiaokang; Dong Yin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 3-Hydroxy-2-oxo-D: AIfriedoolean-3-en-29-oic acid C30H46O4 ÏàËÆ¶È:70% Phytochemistry 1994 36 477-479 1-hydroxy-2, 5, 8-trimethyl-9-fluorenone from Tripterygium wilfordii Xiao Y. Wu, Guo W. Qin, Da J. Fan, Ren S. Xu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . D:A-friedo-3-nor-2,3- secooleanane-2,29-dioic acid C29H46O5 ÏàËÆ¶È:68.9% Helvetica Chimica Acta 2000 Vol. 83 3344 Chemical Constituents of Tripterygium wilfordii Guangzhong Yang, Xueqiang Yin, and Yuanchao Li Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . compound 2a ÏàËÆ¶È:67.8% Australian Journal of Chemistry 1977 30 917-921 Carbon-13 nuclear magnetic resonance spectroscopy of naturally occurring substances. LI. Solanum glycoalkaloids RJ Weston, HE Gottlieb, EW Hagaman and E Wenkert Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 3¦Á-hydroxy-2-oxofriedelane-20¦Á-carboxylic acid C30H48 O4 ÏàËÆ¶È:66.6% Phytochemistry 2001 58 475-480 Dihydroagarofuran alkaloid and triterpenes from Maytenus heterophylla and Maytenus arbutifolia Khaled Y. Orabi, Saleh I. Al-Qasoumi, Mahmoud M. El-Olemy,Jaber S. Mossa, Ilias Muhammad Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 2-hydroxy-3-oxo-friedelan-29-oic acid ÏàËÆ¶È:66.6% Molecules 2009 14 2650-2655 A New Friedelane Type Triterpene from Euonymus hederaceus Cui-Rong Sun, He-Jiao Hu, Run-Sheng Xu, Jie-Hong Yang and Hai-Tong Wan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . wilforic acid F C30H48O4 ÏàËÆ¶È:66.6% Phytochemistry 2000 53 805-810 Triterpenoids from Tripterygium wilfordii Hongquan Duan, Yoshihisa Takaishi, Hiroshi Momota, Yasukazu Ohmoto, Takao Taki, Yongfeng Jia , Duan Li Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-04-25 17:11:49














»Ø¸´´ËÂ¥