| ²é¿´: 332 | »Ø¸´: 1 | ||||
Ë®ÐǤÎÎÀ½ð³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
΢Æ×ÇóÖú
|
|
CÆ×Êý¾Ý£º16.0,18.2,19.0,19.1,19.7,20.5,24.4,26.0,30.7,30.8,31.4,31.8,35.4,37.4,38.0,39.6,39.7,46.3,49.2,55.5,57.8,58.5,61.0,68.0,68.2,68.2,69.3,69.8,71.8,72.1,75.1,76.3,77.6,77.9,78.7,82.7,83.4,83.7,86.3,99.4,100.1,101.7,102.7,109.4,114.1,122.2,140.7 ²âÊÔÈܼÁ£ºC5D5N |
» ²ÂÄãϲ»¶
331Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
081200-11408-276ѧ˶Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
336²ÄÁÏÓ뻯¹¤085600Çóµ÷¼Á
ÒѾÓÐ19È˻ظ´
274Çóµ÷¼ÁÇóµ÷¼Á
ÒѾÓÐ9È˻ظ´
277¡¢Ñ§Ë¶£¬Çóµ÷¼Á ÊýÒ»104£¬
ÒѾÓÐ9È˻ظ´
Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤085600£¬Çóµ÷¼Á
ÒѾÓÐ33È˻ظ´
0854µç×ÓÐÅÏ¢319Çóµ÷¼Á£¨½ÓÊÜ¿çרҵµ÷¼Á£©
ÒѾÓÐ5È˻ظ´
388µ÷¼Á
ÒѾÓÐ3È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
388Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ë®ÐǤÎÎÀ: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ·Ç³£¸Ðл£¡ 2013-09-12 09:35:16
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ë®ÐǤÎÎÀ: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ·Ç³£¸Ðл£¡ 2013-09-12 09:35:16
|
²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½2927¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . stauntoside A C48H72O19 ÏàËÆ¶È:79.1% Phytochemistry 1999 52 1351-1355 Two C21-steroidal glycosides isolated from Cynanchum stauntoi Nanqun Zhu, Mingfu Wang, Hiroe Kikuzaki, Nobuji Nakatani, Chi-Tang Ho Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Argeloside I C48H76O17 ÏàËÆ¶È:77.0% Tetrahedron 2005 61 7470-7480 New antiproliferative 14, 15-secopregnane glycosides from Solenostemma argel Alberto Plaza, Angela Perrone, Ciro Balestrieri, Maria Luisa Balestrieri, Giuseppe Bifulco, Virginia Carbone, Arafa Hamed, Cosimo Pizza, Sonia Piacente Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Argeloside C C49H78O17 ÏàËÆ¶È:75.5% Tetrahedron 2005 61 7470-7480 New antiproliferative 14, 15-secopregnane glycosides from Solenostemma argel Alberto Plaza, Angela Perrone, Ciro Balestrieri, Maria Luisa Balestrieri, Giuseppe Bifulco, Virginia Carbone, Arafa Hamed, Cosimo Pizza, Sonia Piacente Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3-O-[bis-¦Á-L-rhamnopyranosyl-(1¡ú2 and 1¡ú4)-¦Â-D-glucopyranosyl]-25R-furost-5-ene-3b,22¦Á,26-triol C45H74O17 ÏàËÆ¶È:72.3% Planta Medica 2004 70 637-641 Microbial Metabolism of Pseudoprotodioscin Mei Dong,Xizhi Feng,Ben-Xiang Wang, Takashi Ikejima,Li-Jun Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (25R)-spirost-5-en-2¦Á,3¦Â-diol 3-O-¦Á‑L-rhamnopyranosyl-(1¡ú2)-[¦Á‑L-rhamnopyranosyl-(1¡ú4)]-¦Â‑D-glucopyranoside C45H72O17 ÏàËÆ¶È:72.3% Planta Medica 2012 78 276¨C285 Spirostanol Saponins Derivated from the Seeds of Trigonella foenum-graecum by ¦Â-Glucosidase Hydrolysis and Their Inhibitory Effects on Rat Platelet Aggregation Xu Pang, Yue Cong, He-Shui Yu, Li-Ping Kang, Bing Feng, Bing-Xing Han, Yang Zhao, Cheng-Qi Xiong,Da-Wei Tan,Wei Song, Bin Liu, Yu-Wen Cong, Bai-Ping Ma Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (22R,25R)-16¦Â-H-22¦Á-N-spirosol-3¦Â-ol-5-ene 3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-[¦Á-L-rhamnopyranosyl-(1¡ú4)]-¦Â-D-glucopyranoside C45H73NO15 ÏàËÆ¶È:72.3% Phytochemistry 2011 72 668-673 Steroidal alkaloid saponins and steroidal saponins from Solanum surattense Yuanyuan Lu, Jianguang Luo, Lingyi Kong Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . sublanceoside J2 C48H74O18 ÏàËÆ¶È:70.8% Chemical & Pharmaceutical Bulletin 2006 54(11) 1551-1560 Glycosides of 14,15-Seco and 13,14:14,15-Disecopregnanes from the Roots of Cynanchum sublanceolatum Tsutomu WARASHINA and Tadataka NORO Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . solaverine I ÏàËÆ¶È:70.2% Chemical & Pharmaceutical Bulletin 1990 38 827-829 STRUCTURES OF THREE NEW STEROIDAL ALKALOID GLYCOSIDES, SOLAVERINES I, II AND III FROM SOLANUM TOXICARIUM AND S. VERBASCIFOLIUM Tomoyuki YAMASHITA,Nobuyo FUJIMURA,Shoji YAHARA,Toshihiro NOHARA,Syuji KAWANOBU and Kunimitsu FUJIEDA Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (25R) spirost-5-ene-3¦Â,14¦Á-diol-3-¦Â-O-¦Â-L-rhamnopyranosyl(l¡ú 2)-[¦Â-D-xylopyranosyl(l ¡ú 4)]-¦Â-D-glucopyranoside C44H70O17 ÏàËÆ¶È:70.2% Chinese Chemical Letters 2008 19 825-828 Two new steroidal glucosides from Ophiopogon japonicus (L.f.) Ker-Gawl Ya Jiuan Xu, Tun Hai Xu, Ling Zhu Hao, Hong Feng Zhao, Sheng Xu Xie, Yun Shan Si, Dong Han, Dong Ming Xu Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 19 C49H78O18 ÏàËÆ¶È:70.2% Phytochemistry 2000 53 485-498 Steroidal glycosides from the aerial part of Asclepias incarnata Tsutomu Warashina, Tadataka Noro Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . leptinine II C45H73NO16 ÏàËÆ¶È:70.2% Phytochemistry 1998 49 893-897 Steroidal alkaloid glycosides from Solanum orbignianum Rosemary Matias Coelho, Maria Conceição De Souz¦Á, Maria Helena Sarragiotto Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Solamargine ÏàËÆ¶È:70.2% Phytochemistry 1995 39 1475-1477 Steroid alkaloid glycosides from Solanum robustum Helmut Ripperger Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-09-11 21:40:58














»Ø¸´´ËÂ¥