| ²é¿´: 235 | »Ø¸´: 1 | |||
hylgxibÌú¸Ëľ³æ (Ö°Òµ×÷¼Ò)
|
[ÇóÖú]
΢̼Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
| CD3OD£º12.12,15.20,15.70,15.90,18.08,23.26,23.37,23.59,25.13,25.70,25.81,27.45,28.28,31.89,34.57,36.86,39.88,41.52,42.98,45.86,46.86,48.00,48.91,52.96,53.57,61.08,64.02,69.77,72.26,72.48,76.50,76.92,77.17,127.68,138.19,177.18,212.58 |
» ²ÂÄãϲ»¶
272·Ö²ÄÁÏ×ÓÇóµ÷¼Á
ÒѾÓÐ31È˻ظ´
297Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
²ÄÁϹ¤³ÌÈÕÓÉúÇóµ÷¼Á
ÒѾÓÐ5È˻ظ´
¹ã¶«Ê¡ 085601 329·ÖÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
¿¼Ñе÷¼Á
ÒѾÓÐ25È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ18È˻ظ´
µ÷¼Á »¯Ñ§ 307
ÒѾÓÐ17È˻ظ´
²ÄÁÏÀà284µ÷¼Á
ÒѾÓÐ45È˻ظ´
368Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
295·ÖÇóµ÷¼Á
ÒѾÓÐ5È˻ظ´
׿Խ_ÏÈ·æ
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
ºýÍ¿³æ
- Ó¦Öú: 990 (²©ºó)
- ¹ó±ö: 2.955
- ½ð±Ò: 6796.4
- É¢½ð: 12161
- ºì»¨: 82
- ɳ·¢: 17
- Ìû×Ó: 3017
- ÔÚÏß: 2457Сʱ
- ³æºÅ: 1713223
- ×¢²á: 2012-03-24
- ÐÔ±ð: GG
- רҵ: ÁÙ´²Ò©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hylgxib: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-24 14:01:24
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hylgxib: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-24 14:01:24
|
²éѯ½á¹û£º¹²²éµ½6284¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¦Â-D-Glucopyranosyl 3¦Â,19¦Á-dihydroxy-2-oxo-urs-12-en-28-oate C36H56O11 ÏàËÆ¶È:91.8% Natural Product Communications 2009 4 1631-1636 A New ¦Â-D-Glucopyranosyl 2-Oxo-urs-12-en-28-oate fromthe Cameroonian Plant Combretum bracteatum Germain Ntchatcho, Luisella Verotta, Paola Vita Finzi, Giuseppe Zanoni andGiovanni Vidari Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . niga-ichigoside F1 C36H58O11 ÏàËÆ¶È:89.1% Chinese Journal of Natural Medicines 2005 3 17-20 Isolation and Identification of Chemical Constituents from Rubus Parvifolius L. DU Shu-Hu; FENG Fang; LIU Wen-Ying; RAO Jin-Hua; BAI Juan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . kaji-ichigoside F1 ÏàËÆ¶È:86.4% Acta Pharmaceutica Sinica 1996 31 844-848 NEW ELLAGIC GLYCOSIDES AND KNOWN TRITERPENOIDS FROM DUCHESNEA INDICA FOCKE L Ye and JS Yang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 2¦Á,3¦Á,19¦Á-trihydroxy-ursa-12-en-28-oic acid-28-O-¦Â-D-glucopyranosyl ester ÏàËÆ¶È:86.4% China Journal of Chinese Materia Medica 2010 35 3297-3301 Chemical constituents from Callicarpa nudiflora and their hemostatic acitivity ZHANG Jie; LI Baoquan; FENG Feng; TANG Yuping; LIU Wenyuan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . kajiichigoside F ÏàËÆ¶È:86.4% Modern Chinese Medicine 2008 10(3) 10-12 Studies on the chemical constituents of Potentill anserine L. Chu Liang, Wang Libo, Zhang Zhe, Gao Huiyuan, Huang Jian, Sun Bohang, Wu Lijun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . kaji-ichigoside F1 ÏàËÆ¶È:86.4% Journal of China Pharmaceutical University 2002 33 184-187 Studies on the Constituents of Rosa multiflora Thunb LI Yan Fang*; HU Li Hong; LOU Feng Chang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 3¦Â,19¦Á-dihydroxyurs-12-en-28-oic acid 28-¦Â-D-glucopyranoside C36H58O9 ÏàËÆ¶È:86.4% Molecules 2012 17 7629-7636 Terpene Glycosides from the Roots of Sanguisorba officinalis L. and Their Hemostatic Activities Wei Sun, Zi-Long Zhang, Xin Liu, Shuang Zhang, Lu He, Zhe Wang and Guang-Shu Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . kaji-ichigoside F1 C36H58O10 ÏàËÆ¶È:86.4% The Chinese Pharmaceutical Journal 2003 55 179-184 Investigation of the Chemical Constituents of the Roots of Potentilla anserina L. in Tibe Qingwei Li, Jing Hui, Dejing Shang, Lijun Wu and Xiaochi Ma Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . nigaichigoside F1 ÏàËÆ¶È:86.4% Molecules 2013 18 11624-11638 Bioactivity-Guided Fractionation of Physical Fatigue-Attenuating Components from Rubus parvifolius L. Jianhong Chen, Xianfeng Wang, Yongqing Cai, Ming Tang, Qing Dai, Xiaogang Hu, Mingchun Huang, Fengjun Sun, Yao Liu and Peiyuan Xia Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . ¾ßÆÜ¶¬ÇàÜÕ ÏàËÆ¶È:86.4% Chinese Traditional and Herbal Drugs 2011 42 1945-1947 Triterpenoids from barks of Ilex rotunda (I) LUO, Hua-feng, LIN, Chao-zhan, ZHAO, Zhong-xiang, XIONG, Tian-qin, ZHU, Chen-chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . potentillanoside B ÏàËÆ¶È:86.4% Chinese Traditional and Herbal Drugs 2014 45 2742-2747 Chemical constituents from roots of Potentilla anserine LIU Yi, CHENG Liang, HE Quan-quan, YEON Jae-ho, KONG De-yun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . kajiichigoside F1 ÏàËÆ¶È:86.4% Chinese Traditional and Herbal Drugs 2014 45 2742-2747 Chemical constituents from roots of Potentilla anserine LIU Yi, CHENG Liang, HE Quan-quan, YEON Jae-ho, KONG De-yun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . nigaichigoside F1 ÏàËÆ¶È:86.4% Pharmaceutical and Clinical Research 2014 22 231-233 Chemical Components from the Roots of Rubus reflexus Ker. var. lanceolobus Metc HU Jin-ling, HU Zhong-li, LU Zhang-wei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . oblonganoside J C38H60O11 ÏàËÆ¶È:84.2% Journal of Agricultural and Food Chemistry 2007 55 1712-1717 Anti-Tobacco Mosaic Virus (TMV) Triterpenoid Saponins from the Leaves of Ilex oblonga Zu-Jian Wu, Ming-An Ouyang, Cong-Zhou Wang, Zheng-Kun Zhang, and Jian-Guo Shen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . callianthaside A C36H58O11 ÏàËÆ¶È:83.7% Helvetica Chimica Acta 2007 Vol. 90 2421 Phenolic and Triterpenoid Glycosides from Pyrola calliantha Yi-Lei Chen, Chang-Heng Tan, Jun-Jie Tan, Shi-Jin Qu, Heng-Bin Wang, Qiang Zhang, Shan-Hao Jiang, and Da-Yuan Zhu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (20S)-niga-ichigoside F1 C36H58O11 ÏàËÆ¶È:83.7% Journal of Natural Products 2005 68 1531-1535 |

2Â¥2015-04-24 12:34:31













»Ø¸´´ËÂ¥