| ²é¿´: 473 | »Ø¸´: 1 | ||
fengfajinгæ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖú΢Æ×£¬Ð»Ð»~~~лл~~~ ÒÑÓÐ1È˲ÎÓë
|
|
»¯ºÏÎïfr8 13 NMR(DMSO-d6, 100MHz) 29.02,44.96,63.23,69.73,73.16,74.05,76.49,94.64,96.95,100.76,105.30,113.94,114.84,114.96,115.78,125.07,129.10,130.19,131.50,132.66,144.81,155.26,159.80,160.58,164.34,165.21,166.44,204.65 |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ4È˻ظ´
±¾9Ò»Ö¾Ô¸2 0854µÍ·Öר˶286Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
298Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
²ÄÁÏרҵ344Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
282£¬µçÆø¹¤³Ìרҵ£¬Çóµ÷¼Á£¬²»Ìôרҵ
ÒѾÓÐ6È˻ظ´
301Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ28È˻ظ´
²ÄÁÏ085601µ÷¼Á
ÒѾÓÐ17È˻ظ´
Ò»Ö¾Ô¸0703»¯Ñ§ÕÐ61×îÖÕÅÅÃû62»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ23È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
ÇóÖú¡¢¡¢¡¢Ð»Ð»´óÉñ
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬ÀàËÆéÎÆ¤ËصĶà¶à¸ø
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬¿É·ñÓÐÈËÖ¸µã»òÔõÑù²éµ½´øÓÐÒÑÖªµ¥ÌåµÄºË´ÅÆ×Êý¾ÝÎÄÏ×
ÒѾÓÐ4È˻ظ´
ÇóÖúÒ»»¯ºÏÎï΢Æ×Êý¾Ý½á¹¹
ÒѾÓÐ10È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»df12
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú(±½»·ÑÜÉúÎïÀà)
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
- ºì»¨: 21
- Ìû×Ó: 2773
- ÔÚÏß: 261.2Сʱ
- ³æºÅ: 942922
- ×¢²á: 2010-01-15
- ÐÔ±ð: MM
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
fengfajin: ½ð±Ò+10, ¡ïÓаïÖú, OK 2015-05-12 13:50:34
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
fengfajin: ½ð±Ò+10, ¡ïÓаïÖú, OK 2015-05-12 13:50:34
|
1 . kaempferol 3-O-(6''-O-E-p-coumaroyl)-¦Â-D-glucopyranoside ÏàËÆ¶È:71.4% Journal of China Pharmaceutical University 2007 38 315-319 Chemical constituents of the aerial parts of Euphorbia sororia ZHANG Wei-ku; ZHANG Xiao-qi; YE Wen-cai; Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . kaempferol 3-O-¦Â-D-(6''-O-E-4-coumaroyl) glucopyranoside C30H26O13 ÏàËÆ¶È:70% Natural Product Research 2001 15 1-8 Flavonol Glycosides from Elaeagnus bockii (Elaeagnaceae) Shu-Geng Cao; Toshiyuki Tanaka; Mizuo Mizuno; Kenichiro Inoue Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . ɽèÍ·Ó-3-O-¦Â-D-6-D-(¶ÔôÇ»ù¹ðƤõ£»ù)-ßÁà«ÆÏÌÑÌÇÜÕ C30H26O13 ÏàËÆ¶È:70% Chinese Traditional and Herbal Drugs 2008 39 671-672 ºúÍÇ×ÓÒ¶»¯Ñ§³É·ÖÑо¿ ¸¶Òå³É;ÍõÏþ¾²;¼ÖÏ×»Û;Àî¿¡æ¼ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . kaempferol-3-O-¦Â-D-6-O-(p-hydroxycinnamoyl)-glucopyranoside C30H26O13 ÏàËÆ¶È:70% Journal of Chinese Medicinal Materials 2009 32 1848-1850 Primary Studies on Chemical Constituents from Butanol Extraction of the Thorny Elaeagnus Leaf and Their Cytotoxicity FU Yi-cheng, WANG Xiao-jing, JIA Xian-hui, ZHOU Ling Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . tiliroside ÏàËÆ¶È:70% Journal of Shenyang Pharmaceutical University 2011 28 520-525 Isolation and identification of chemical constituents from the flowers of Abelmoschus manihot(L.) Medic (III) LI, Chun-mei, AN, Ya-ting, WANG, Tao, SHANG, Hai-hua, GAO, Xiu-mei, ZHANG, Yi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . kaempferol 3-O-[2'',6''-di-O-(trans-p-coumaroyl)]-¦Â-D-glucopyranosdie C39H32O15 ÏàËÆ¶È:68.9% Indian Journal of Chemistry Section B 2001 40B 394-398 Flavonoids from the leaves of Quercus dentata Ying-Jun Zhou, Sui-Xu Xu, Qing-Ming Che, Qi-shi Sun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . hispidulin 7-(6-E-p-coumaroyl-¦Â-D-glucopyranoside) C31H28O13 ÏàËÆ¶È:67.8% Phytochemistry 2002 61 405-408 Flavonoids from the aquatic plant Eriocaulon buergerianum Jiau-Ching Ho, Chiu-Ming Chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . apigenin-4'-O-(2", 6"-di-O-trans-p-coumaroyl)-D-glucoside C39H42O14 ÏàËÆ¶È:67.8% Planta Medica 1979 36 196-199 A New Acylated Apigenin 4'-O-¦Â-D-glucoside from the Leaves of Lycopodium clavatum L. Faizur Rahman Ansari, Wajid Husain Ansari, Wasiur Rahrnan,O. Seligmann, V. M. Chari, H. Wagner and B. G. asterdahl Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . tiliroside ÏàËÆ¶È:67.8% China Journal of Chinese Materia Medica 2005 30 516-518 Study on flavonoids from leaf of Ipomoea batatas LUO Jianguang, KONG Lingyi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 3-O-¦Â-D-ßÁà«ÆÏÌÑÌÇ-(6-O-¶ÔôÇ»ù·´Ê½Ïã¶¹õ£»ù)-ɽÝÁËØÜÕ ÏàËÆ¶È:67.8% China Journal of Chinese Materia Medica 2001 26 549-551 Chemical Constituents from the Fruit of Rosa bella Rehd. et Wils CHEN Fengzheng, PENG Shulin, DING Lisheng, HE Yonghua, WANG Mingkui |
2Â¥2015-05-08 08:18:34













»Ø¸´´ËÂ¥