| ²é¿´: 221 | »Ø¸´: 1 | ||
ÊÇÌØÒ»×åľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú
|
|
10.7,17.1,17.2,17.2,17.3,17.9,18.7,19.3,22.6,28.1,28.6,35.5,37.7,37.7,39.5,40.0,41.7,43.8,44.8,50.2,56.4,63.5,69.7,71.6,72.2,74.0,75.4,75.9,76.2,78.9,79.0,79.5,89.1,103.2,107.4,120.7,123.4,135.5,149.8,180.1 ÈܼÁ£ºC5D5N£¨¼ÇµÃÑ¡ÔñÈܼÁ£© |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ23È˻ظ´
301Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
304Çóµ÷¼Á£¨085602£¬¹ýËļ¶£¬Ò»Ö¾Ô¸985£©
ÒѾÓÐ17È˻ظ´
302·ÖÇóµ÷¼Á Ò»Ö¾Ô¸°²»Õ´óѧ085601
ÒѾÓÐ12È˻ظ´
288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò
ÒѾÓÐ23È˻ظ´
»·¾³×¨Ë¶µ÷¼Á
ÒѾÓÐ6È˻ظ´
22408 µ÷¼Á²ÄÁÏ
ÒѾÓÐ6È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600²ÄÁÏÓ뻯¹¤301·ÖÇóµ÷¼ÁԺУ
ÒѾÓÐ19È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÊÇÌØÒ»×å: ½ð±Ò+5, ¡ï¡ï¡ïºÜÓаïÖú 2013-12-09 23:02:41
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÊÇÌØÒ»×å: ½ð±Ò+5, ¡ï¡ï¡ïºÜÓаïÖú 2013-12-09 23:02:41
|
²éѯ½á¹û£º¹²²éµ½2762¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . dunnianaolactone B C41H66O14 ÏàËÆ¶È:73.1% Helvetica Chimica Acta 2011 94 2207-2214 Three New E-Secoursane Triterpenoid Saponins from the Leaves of Ilex dunniana (pages 2207¨C2214) Yue Zhang, Lu-Jun Li, Peng Zhang, Hui-Fang Pi, Han-Li Ruan and Ji-Zhou Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . mabioside A ÏàËÆ¶È:71.4% Natural Product Research 1993 2 203-207 Mabioside B, A Novel Saponin from Colubrina Elliptica Ali Oulad-ali; Dominique Guillaume; Yulin Jiang; Bernard Weniger; Robert Anton Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . mabioside B C42H66O15 ÏàËÆ¶È:70.7% Natural Product Research 1993 2 203-207 Mabioside B, A Novel Saponin from Colubrina Elliptica Ali Oulad-ali; Dominique Guillaume; Yulin Jiang; Bernard Weniger; Robert Anton Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . gypenbioside A C41H66O13 ÏàËÆ¶È:70.7% Journal of Asian Natural Products Research 2012 14 856-861 Two new triterpene saponins from Gynostemma pentaphyllum Lin Shi, Fei Lu, Hong Zhao & Yu-Qing Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . hoduloside VI C41H68O14 ÏàËÆ¶È:68.2% Chemical & Pharmaceutical Bulletin 1993 41 1722-1725 Antisweet Natural Products. VIII. Structures of Hodulosides VI-X from Hovenia dulcis THUNB. var. tomentella MAKINO Kazuko YOSHIKAWA,Yasuhiro NAGAI,Masaya YOSHIDA and Shigenobu ARIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . cornutaosid B C41H68O15 ÏàËÆ¶È:68.2% Food Chemistry 2008 111 78-82 Two unusual minor 18,19-seco-ursane glycosides from leaves of Ilex cornuta Tao Wu, Yan Li, Qing-jiu Tang, Zheng-tao Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . eclalbasaponin VII C36H62O8 ÏàËÆ¶È:67.5% Phytochemistry 1997 44 131-135 Taraxastane glycosides from Eclipta alba Shoji Yahara, Ning Ding, Toshihiro Nohara, Kazuo Masuda, Hiroyuki Ageta Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . peniciside C38H62O10 ÏàËÆ¶È:67.5% Archives of Pharmacal Research 2012 35 311-314 Peniciside, a new triterpenoid glycoside, from the fungus Penicillium sp. 169 Xiao-Hong Yuan, Guo-Bo Xu, Wei-Lin Wu, Tao Yang and Guo-You Li Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3¦Â-[(¦Á-L-arabinopyranosyl)oxy]-urs-11,13(18)-dien-28-oic acid ¦Â-D-glucopyranosyl ester C41H64O12 ÏàËÆ¶È:65.8% Phytochemistry 2005 66 1671-1679 Triterpenoids from Sanguisorba officinalis Xin Liu, Yanxing Cui, Qiang Yu, Biao Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Dexyloprimulanin C41H66O13 ÏàËÆ¶È:65.8% Phytochemistry 2011 72 2075-2080 Alkyl phenols and saponins from the roots of Labisia pumila (Kacip Fatimah) Zulfiqar Ali, Ikhlas A. Khan Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (3¦Â,20S,23S)-3,20,23-trihydroxydammar-24-en-21-oic acid-21,23-lactone 3-O-¦Â-D-xylopyranosyl-(1¡ú3)-¦Â-D-glucopyranoside C41H66O13 ÏàËÆ¶È:65.8% Journal of Natural Products 2012 75 1373-1382 Dammarane Glycosides from the Root of Machilus yaoshansis Maoluo Gan, Mingtao Liu, Lishe Gan, Sheng Lin, Bo Liu, Yanling Zhang, Jiachen Zi, Weixia Song, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . gypenbioside B C41H66O13 ÏàËÆ¶È:65.8% Journal of Asian Natural Products Research 2012 14 856-861 Two new triterpene saponins from Gynostemma pentaphyllum Lin Shi, Fei Lu, Hong Zhao & Yu-Qing Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . borassoside D C39H62O12 ÏàËÆ¶È:65% Chemical & Pharmaceutical Bulletin 2007 55(2) 308-316 Medicinal Flowers. XII.1) New Spirostane-Type Steroid Saponins with Antidiabetogenic Activity from Borassus flabellifer Masayuki YOSHIKAWA,Fengming XU,Toshio MORIKAWA,Yutana PONGPIRIYADACHA,Seikou NAKAMURA,Yasunobu ASAO,a Akira KUMAHARA,and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (25R)-26-O-¦Â-D-glucopyranosyl-furost-1¦Â,3¦Â,5¦Â,22¦Á,26-pentaol-3-O-¦Â-D-glucoside C39H66O16 ÏàËÆ¶È:65% Magnetic Resonance in Chemistry 2009 47 613-616 Structural elucidation and NMR spectral assignment of three new furostanol saponins from the roots of Tupistra chinensis (pages 613¨C616) Zhiyong Guo, Kun Zou, Junzhi Wang, Chuang Liu, Zichun Tang and Chunyan Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 28-O-¦Â-D-Glucopyranosylbetulin 3¦Â-O-¦Â-D-glucopyranoside C42H70O12 ÏàËÆ¶È:64.2% Journal of Natural Products 2009 72 72-81 Synthesis and Cytotoxicity of Bidesmosidic Betulin and Betulinic Acid Saponins Charles Gauthier,Jean Legault,Serge Lavoie, Simon Rondeau, Samuel Tremblay, and Andr¨¦ Pichette Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . sapinmusaponin O C42H72O12 ÏàËÆ¶È:64.2% Phytochemistry 2008 69 1609-1616 Triterpenoid saponins from the fruits and galls of Sapindus mukorossi Hui-Chi Huang,Ming-Der Wub,Wei-Jern Tsai,Sin-Chung Liao,Chia-Ching Liaw,Li-Chuan Hsu,Yang-Chang Wua,Yao-Haur Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . sapinmusaponin P C42H72O12 ÏàËÆ¶È:64.2% Phytochemistry 2008 69 1609-1616 Triterpenoid saponins from the fruits and galls of Sapindus mukorossi Hui-Chi Huang,Ming-Der Wub,Wei-Jern Tsai,Sin-Chung Liao,Chia-Ching Liaw,Li-Chuan Hsu,Yang-Chang Wua,Yao-Haur Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . prosaikogenin C-2 C42H38O12 ÏàËÆ¶È:64.2% Chemical & Pharmaceutical Bulletin 1989 37 1293-1296 New Derivatives of Saikosaponin c Mitsuhiko NOSE,Sakae AMAGAYA,Tadahiro TAKEDA and Yukio OGIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 20(S)-dammar-24-ene-3¦Â,20,26-triol 3-O-¦Â-D-glucopyranoside C36H62O8 ÏàËÆ¶È:64.2% Chemical & Pharmaceutical Bulletin 1985 33 1400-1406 Studies on the Constituents of Hedera rhombea BEAN. II. On the Dammarane Triterpene Glycosides. (1) HARUHISA KIZU,MICHIYO KOSHIJIMA,MASATOMI HAYASHI and TSUYOSHI TOMIMORI Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Mabioside D C42H70O14 ÏàËÆ¶È:64.2% Phytochemistry 1994 36 445-448 Mabiosides C-E: triterpenoid saponins from the bark of Colubrina elliptica Ali Oulad-Ali, Dominique Guillaume, Bernard Weniger, Yulin Jiang, Robert Anton Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ilekudinoside L C41H64O14 ÏàËÆ¶È:63.4% Journal of Natural Products 2005 68 1169-1174 Triterpene Saponins from the Leaves of Ilex kudingcha Li Tang, Yong Jiang, Hai-Tao Chang, Ming-Bo Zhao, Peng-Fei Tu, Jing-Rong Cui, and Rui-Qing Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . compound 1 C42H68O15 ÏàËÆ¶È:63.4% Journal of Natural Products 2002 65 1560-1567 Acylated Triterpenoid Saponins from the Stem Bark of Foetidia africana Marie-Laure Crublet,Isabelle Pouny, Cl¨¦ment Delaude, and Catherine Lavaud Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 3-O-¦Â-D-glucopyranosyl-(1¡ú3)-¦Â-Dglucuronopyranosyl-29-hydroxyoleanolic acid-28-O-¦Â-D-glucopyranoside C48H76O20 ÏàËÆ¶È:63.4% Journal of Natural Products 2000 63 1261-1264 Triterpene Saponins, Quaternary Ammonium Compounds, Phosphatidyl Cholines, and Amino Acids in the Pronotal and Elytral Secretions of Platyphora opima and Desmogramma subtropica V. Plasman, J. C. Braekman,D. Daloze, D. Windsor, and J. M. Pasteels Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . cincholic acid 3¦Â-O-¦Â-6-deoxy-D-glucopyranoside-28-O-¦Â-D-glucopyranoside C42H66O14 ÏàËÆ¶È:63.4% Phytochemistry 1990 29 209-213 Two triterpene glycosides from Isertia haenkeana F.Javier Arriaga,Angel Rumbero,Purificacion Vazquez Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-12-09 10:34:07














»Ø¸´´ËÂ¥
10