| ²é¿´: 430 | »Ø¸´: 1 | ||
libinoookľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý 4-8 ÒÑÓÐ1È˲ÎÓë
|
| 13C NMR (126 MHz, cd3od) ¦Ä17.83,70.73,72.20,73.49,73.78,94.70,99.84,100.53,105.87,110.36,116.48,116.89,121.25,122.83,124.96,135.64,139.95,146.43,146.49,149.88,158.51,159.26,163.22,165.86,167.43,179.40 |
» ²ÂÄãϲ»¶
327Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
08¹¤¿ÆÇóµ÷¼Á290·Ö
ÒѾÓÐ11È˻ظ´
Ò»Ö¾Ô¸985³õÊÔ354·ÖÉúÎïµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸2110£¬»¯Ñ§Ñ§Ë¶310·Ö£¬±¾¿ÆÖصãË«·ÇÇóµ÷¼Á
ÒѾÓÐ13È˻ظ´
353Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
308Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
334Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
Ò»Ö¾Ô¸0807 ÊýÒ»Ó¢Ò» 313 ÓÐûÓжþÂÖµ÷¼Á
ÒѾÓÐ7È˻ظ´
¸´ÊÔµ÷¼Á£¬Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤289·Ö
ÒѾÓÐ14È˻ظ´
086000µ÷¼Á
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý4¸ö
ÒѾÓÐ6È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻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
libinoook: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-06-10 22:02:36
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
libinoook: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-06-10 22:02:36
|
quercetin 3-rhamnoside 2''-gallate ÏàËÆ¶È:92.3% Chinese Pharmaceutical Journal 2000 35 300-302 Studies on the chemical constituents of flavonoids from Polygonum capitatum Li Yongjun(Li YJ), Luo Hongfeng(Luo HF), Wang Yonglin(Wang YL), et al Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . quercetin-3-O-2''-galloyl-rhamnoside C28H24O15 ÏàËÆ¶È:92.3% Chinese Traditional and Herbal Drugs 2013 44 803-807 Chemical constituents from barks of Pterocarya stenoptera GAO Shuang, YE Kai-he, ZHANG Ying, ZHOU Guang-xiong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . compound 1 ÏàËÆ¶È:84.6% Bioscience, Biotechnology, and Biochemistry 2001 65 1302-1309 Isolation and Antioxidant Activity of Galloyl Flavonol Glycosides from the Seashore Plant, Pemphis acidula Toshiya MASUDA, Kumiko IRITANI, Shigetomo YONEMORI, Yasuo OYAMA, Yoshio TAKEDA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . éÎÆ¤ËØ-3-O-(2-O-ûʳ×Óõ£»ù)-¦Á-L-ßÁà«ÊóÀîÌÇ ÏàËÆ¶È:84.6% Journal of Chinese Medicinal Materials 1995 18 297-301 Studies on the Polyphenol Constituents of Ampelopsis japonica (part ¢ò) Yu Wensheng, Chen Xinmin, Yang Lei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . quercetin-3-O-¦Á-(2''-digalloyl)-arabinopyranoside C27H22O15 ÏàËÆ¶È:84.6% Chinese Traditional and Herbal Drugs 2012 43 1496-1498 Chemical constituents from Euphorbia stracheyi ZHANG Ben-yin; WANG Huan; LUO Xiao-dong; DU Zhi-zhi; SHEN Jian-wei; ZENG Ling-feng; ZHANG Xiao-feng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . quercetin 3-O-(2''-galloyl)-¦Â-D-galactopyranoside ÏàËÆ¶È:81.4% Journal of Natural Products 1998 61 145-148 A New Flavonol Glycoside Gallate Ester from Acer okamotoanum and Its Inhibitory Activity against Human Immunodeficiency Virus-1 (HIV-1) Integrase Hyoung Ja Kim, Eun-Rhan Woo, Cha-Gyun Shin, and Hokoon Park Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . myricetin 3-O-(2''-O-p-hydroxybenzoyl)-¦Á-rhamnopyranoside C28H23O14 ÏàËÆ¶È:80.7% Planta Medica 2000 66 382-383 Flavonoids and Phenolics from Limonium sinense Lie-Chwen Lin,Cheng-Jen Chou |
2Â¥2015-06-10 19:43:46













»Ø¸´´ËÂ¥