| ²é¿´: 232 | »Ø¸´: 1 | ||
µØ¹ÏµØ¹Ï½ð³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
| 23.762,25.252,25,683,25.940,27.301,27.835,28.068,28.208,32.498,32.674,34.635,37.697,37.974,38.066,38.153,39.524,39.845,40.919,41.078,41.335,41.691,43.887,53.749,65.761,72.246,78.714,81.177,123.320,127.862,138.791 |
» ²ÂÄãϲ»¶
319Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
081700»¯Ñ§¹¤³ÌÓë¼¼Êõ Ò»Ö¾Ô¸Öк£Ñó 323 Çóµ÷¼ÁѧУ
ÒѾÓÐ15È˻ظ´
085600£¬320·ÖÇóµ÷¼Á
ÒѾÓÐ14È˻ظ´
085600µ÷¼Á
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á£º085600²ÄÁÏÓ뻯¹¤£¬¿¼²Ä¿Æ»ù£¬×Ü·Ö319
ÒѾÓÐ26È˻ظ´
0703»¯Ñ§
ÒѾÓÐ5È˻ظ´
085600£¬×¨Òµ¿Î»¯¹¤ÔÀí£¬320·ÖÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸ÄÏÅ©090401£¬268£¬Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁÏ334Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
323Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48394.9
- ºì»¨: 52
- Ìû×Ó: 6742
- 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 ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
µØ¹ÏµØ¹Ï: ½ð±Ò+10, ¡ïÓаïÖú 2014-12-11 12:30:25
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
µØ¹ÏµØ¹Ï: ½ð±Ò+10, ¡ïÓаïÖú 2014-12-11 12:30:25
|
1 . 2¦Á,3¦Á,19¦Á,23-Tetrahydroxyurs-12-en-28-oic Acid ÏàËÆ¶È:67.7% Journal of Asian Natural Products Research 2003 5 49-56 BIOACTIVE TRITERPENOIDS FROM SYMPLOCOS CHINENSIS XI-HAO LI, DIAN-DIAN SHEN, NAN LI and SHI-SHAN YU Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . euscaphic acid ÏàËÆ¶È:67.7% Natural Product Research 2008 22 1310-1316 Two new 11¦Á,12¦Á-epoxy-ursan-28,13¦Â-olides and other triterpenes from Cecropia catharinensis E. C. Machado; R. A. Yunes; A. Malheiros; E. C. Gomez; F. Delle Monache Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . euscaphic acid ÏàËÆ¶È:67.7% Pharmazie 2008 63 765-767 Euscaphic acid, a new hypoglycemic natural product from Folium Eriobotryae Jian Chen, Wei-Lin Li, Ju-Lan Wu, Bing-Ru Ren and Han-Qing Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . euscaphic acid ÏàËÆ¶È:67.7% 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 ̼Æ×Ä£Äâͼ 5 . euscaphic acid ÏàËÆ¶È:67.7% Journal of Peking University (Health Sciences) 2004 36 21-23 Studies on the chemical constituents from Potentilla multifida L. XUE Pei feng; QIAO Liang; LIANG Hong; ZHAO Yu ying Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . euscaphic acid ÏàËÆ¶È:67.7% 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 ̼Æ×Ä£Äâͼ 7 . ilexpernoside J C48H78O20 ÏàËÆ¶È:64.5% Helvetica Chimica Acta 2008 Vol. 91 1630 Triterpene Saponins from the Leaves of Ilex pernyi Guang-Bo Xie, Jiao Zheng, Peng-Fei Tu, and Guo-Qing Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 9 ÏàËÆ¶È:64.5% Journal of Natural Products 1996 59 304-307 Triterpenoids from Adina rubella Shi-yue Fang, Zhi-sheng He, and Gao-jun Fan, Hou-ming Wu and Jing-fei Xu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 5 C31H50O4 ÏàËÆ¶È:64.5% Planta Medica 1998 64 189-191 Kalaic Acid, A New Ursane-Type Saponin from Musanga cecroploides D. Lontsi, B. L. Sondengam, B. Bodo, and M. 1. Martin Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . pomolic acid methylate ÏàËÆ¶È:64.5% Chemical & Pharmaceutical Bulletin 1978 26 2689-2693 Studies on the Constituents of the Medicinal Plants. XXI. Constituents of the leaves of Clethra barbinervis SIEB. et ZUCC. (2) and the 13C-Nuclear Magnetic Resonance Spectra of 19¦Á-Hydroxyurs-12-en-28-oic Acid Type of Triterpenoids KOTARO TAKAHASHI and MASAKO TAKANI Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 3a ÏàËÆ¶È:64.5% Chemical & Pharmaceutical Bulletin 1987 35 524-529 New Triterpene Saponins from Ilex pubescens KAZUYUKI HIDAKA,MIYOKO ITO,YOKO MATSUDA,HIROSHI KOHDA,KAZUO YAMASAKI,JOHJI YAMAHARA,TAKESHI CHISAKA,YOSHIYUKI KAWAKAMI,TADASHI SATO and KENGO KAGEI Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . methyl pomolate ÏàËÆ¶È:64.5% Chemical & Pharmaceutical Bulletin 1987 35 841-845 Two New Triterpenoid Glycosides from Leaves of Ilex chinensis SIMS AKIRA INADA,MARI KOBAYASHI,HIROKO MURATA and TSUTOMU NAKANISHI Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 21¦Á-Hydroxyoleanolic acid ÏàËÆ¶È:64.5% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 3¦Â,19-dihydroxyolean-12-en-28-oic acid C30H48O4 ÏàËÆ¶È:64.5% Acta Botanica Boreali-Occidentalia Sinica 2007 27 1141-1146 The Triterpenes in Salvia umbratica LIU Qing, LIU Zhen-ling, TIAN Xuan Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . glyyunnansapogenin B2 ÏàËÆ¶È:64.5% Acta Pharmaceutica Sinica 1995 30 27-33 NEW TRTEKPENOIDAL SAPOGENINS FROM THE ROOTS OF GLYCYRRHIZA YUNNANENSIS JF Hu; ZL Ye and FJ Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . pomolic acid ÏàËÆ¶È:64.5% China Journal of Chinese Materia Medica 2005 30 1833-1836 Triterpenes from root of Rhaponticum uniflorum ZHANG Yonghong, ZHANG Jiangang, XIE Jieming, CHEN Gelin, CHENG Dongliang Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . pomolic acid ÏàËÆ¶È:64.5% 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 Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . euscaphic acid methyl ester C31H50O4 ÏàËÆ¶È:64.5% Phytochemistry 1997 46 549-554 Triterpenes from Paliurus hemsleyanus Shoei-Sheng Lee, Shew-Neu Shy, Karin C. S. Liu Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-12-11 11:54:57














»Ø¸´´ËÂ¥