| ²é¿´: 272 | »Ø¸´: 1 | ||
hylgxibÌú¸Ëľ³æ (Ö°Òµ×÷¼Ò)
|
[ÇóÖú]
΢̼Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
| CD3OD£º11.59,15.18,16.52,18.06,21.00,23.41,25.17,25.69,25.84,26.91,27.69,28.34,32.79,36.92,37.54,40.62,41.21,41.51,42.97,47.86,48.08,53.45,61.16,69.81,70.46,72.28.72.50,76.93,77.17,79.30,79.97,94.39,129.54,137.06,177.18 |
» ²ÂÄãϲ»¶
296Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
295Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
297Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
303Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
314Çóµ÷¼Á
ÒѾÓÐ18È˻ظ´
¹ã¶«Ê¡ 085601 329·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
272·Ö²ÄÁÏ×ÓÇóµ÷¼Á
ÒѾÓÐ24È˻ظ´
ÖÐҩѧµ÷¼Á ³õÊÔ324
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸¾©Çø985£¬085401£¬Óë±¾¿Æ×¨ÒµÒ»Ö£¬µç×ÓÐÅÏ¢¹¤³Ì£¬
ÒѾÓÐ4È˻ظ´
284Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48426.9
- ºì»¨: 52
- Ìû×Ó: 6748
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hylgxib: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-23 07:24:12
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hylgxib: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-23 07:24:12
|
1 . kaji-ichigoside F1 ÏàËÆ¶È:80.5% 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 2 . 1¦Â,2¦Á,3¦Á-trihydroxyurs-12-en-28-oic acid (1¦Â-hydroxyeuscaphic acid) C30H48O6 ÏàËÆ¶È:77.1% Natural Product Sciences 2009 15 76-82 NMR Assignment and Antimicrobial/Antioxidant Activities of 1¦Â-Hydroxyeuscaphic acid from the Seeds of Butyrospermum parkii Nyaa, Laurentine Bouquet Tankeu; Tapondjou, Leon Azefack; Barboni, Luciano; Tamokou, Jean De Dieu; Kuiate, Jules Roger; Tane, Pierre; Park, Hee-Juhn Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . emarginellic acid C30H18O5 ÏàËÆ¶È:75% Phytochemistry 2006 67 956-964 Crotalic and emarginellic acids: Two triterpenes from Crotalaria emarginella and anti-inflammatory and anti-hepatotoxic activity of crotalic acid Bahar Ahmed , Tawfeq A. Al-Howiriny, Jaber S. Mossa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . kaji-ichigoside F1 C36H60O10 ÏàËÆ¶È:75% Chinese Journal of Natural Medicines 2010 8 12-15 Triterpenoids from the Roots of Rose odorata var.gigantean LIU Dai-Lin; ZHU Shan; MA Rong; ZHANG Jing-Ze; LI He-Yu; CHEN Hong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . potentillanoside A C36H56O10 ÏàËÆ¶È:75% Phytochemistry 2014 102 169-181 Hepatoprotective triterpenes from traditional Tibetan medicine Potentilla anserina Toshio Morikawa, Kiyofumi Ninomiya, Katsuya Imura, Takahiro Yamaguchi, Yoshinori Akagi, Masayuki Yoshikawa, Takao Hayakawa, Osamu Muraoka Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . ilexsaponin B C36H56O11 ÏàËÆ¶È:75% Asian Journal of Chemistry 2013 25 9457-9459 Qtriterpenoides from the Leaves of Ilex pubescens and their Potential Xanthine Oxidase Inhibitory Activity ZHONG-LIU ZHOU, *, ZONG-CAI FENG and JING-MIN XIA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . methyl-1¦Á,2¦Á,3¦Â,19¦Á-tetrahydroxyurs-12-en-28-oate C31H50O6 ÏàËÆ¶È:74.2% Phytochemistry 1998 49 2477-2481 Pentacyclic triterpenoids from Rubus xanthocarpus Bao-Zhi Li, Bin-Gui Wang, Zhong-Jian Jia Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . derivative of methyl tormentate C35H54O7 ÏàËÆ¶È:74.2% Phytochemistry 1998 48 171-174 Cecropioic acid, a pentacyclic triterpene from Musanga cecropioides D. Lontsi, B. L. Sondengam, M. T. Martin, B. Bodo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . niga-ichigosideF1 ÏàËÆ¶È:74.2% Natural Product Research and Development 2014 26 215-217 Chemical Constituents from the Water-soluble Fraction of Rabdosia excisa TANG Jian, MA Rui-li, LIU Hong-chuan, OUYANG Zhen, CHEN Hai-sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . rubuside J C36H56O11 ÏàËÆ¶È:72.2% Journal of Natural Products 2009 72 1755-1760 Triterpenoid Saponins from Rubus ellipticus var. obcordatus Wei Li, Hongwei Fu, Hong Bai, Tatsunori Sasaki, Hiroyoshi Kato, and Kazuo Koike Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . ilexoside XXX C36H56O11 ÏàËÆ¶È:72.2% Chemical & Pharmaceutical Bulletin 1992 40 3138-3141 Triterpenoid Saponins of Aquifoliaceous Plants. VIII. Ilexosides XXIX-XXXII from the Leaves of Ilex rotunda THUNB. Kayoko AMIMOTO,Kazuko YOSHIKAWA and Shigenobu ARIHARA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 2 ÏàËÆ¶È:72.2% Phytochemistry 1996 42 505-508 Unsaturated E-ring triterpenes from rubus pinfaensis David G. Durham, Iain X. Liu, R. Michael E. Richards Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-04-22 18:03:58













»Ø¸´´ËÂ¥