| ²é¿´: 635 | »Ø¸´: 1 | |||
shaoyan415гæ (СÓÐÃûÆø)
|
[ÇóÖú]
GS8---CÆ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
| 13C NMR (125 MHz, Pyr) ¦Ä 14.04,16.28,16.33,17.10,17.36,19.25,19.42,20.01,20.10,22.30,23.35,27.54,28.19,28.44,28.54,29.66,35.07,35.30,38.66,39.96,39.98,46.68,47.17,48.11,48.55,49.31,49.79,51.90,54.35,56.64,69.07,72.00,76.83,77.34,125.53,141.38,154.18,161.38,178.46,199.97,208.16 |
» ²ÂÄãϲ»¶
µ÷¼ÁÇóÊÕÁô
ÒѾÓÐ7È˻ظ´
272·Ö²ÄÁÏ×ÓÇóµ÷¼Á
ÒѾÓÐ36È˻ظ´
275Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
070300»¯Ñ§Ñ§Ë¶311·ÖÇóµ÷¼Á
ÒѾÓÐ19È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ13È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ33È˻ظ´
¸´ÊÔµ÷¼Á
ÒѾÓÐ7È˻ظ´
Ò»Ö¾Ô¸¹þ¹¤´ó 085600 277 12²Ä¿Æ»ùÇóµ÷¼Á
ÒѾÓÐ17È˻ظ´
»¹Óл¯¹¤¶þÂÖµ÷¼ÁµÄѧУÂð
ÒѾÓÐ47È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖúOrigin8´¦ÀíÒºÏàÉ«Æ×ͼ
ÒѾÓÐ17È˻ظ´
origin8.0¶ÔÀÂüÆ×·Ö·åÓöµ½Âé·³ÁË£¬ÇóÖú
ÒѾÓÐ6È˻ظ´
¼±¼±¼±£¡ºË´ÅCÆ×ÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú£ºÒºÏàÉ«Æ×Öù£¬Öù×ÓΪ waters Sunfire TM C18
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð» £¨TE1-1£©
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý YC-8
ÒѾÓÐ7È˻ظ´
΢Æ×ÇóÖú£¬ÔÚÏßµÈ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúoriginÈçºÎ»Èýάӫ¹â¹âÆ×ͼ
ÒѾÓÐ25È˻ظ´
ÇóÖú½âÎöÒ»»¯ºÏÎïµÄHÆ×CÆ×£¬¸½ÉÏͼÆ×
ÒѾÓÐ13È˻ظ´
ÇóÖú HÆ×ºÍCÆ×
ÒѾÓÐ15È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú½âÆ×CÆ×ºÍHÆ×
ÒѾÓÐ22È˻ظ´
¡¾ÇóÖú¡¿ÇóÈ˰ïæ·ÖÎöÒ»ÏÂxps C 1sÆ×ͼ
ÒѾÓÐ11È˻ظ´
¡¾ÇóÖú¡¿ÇëÎÊ C-O-O-CºìÍâ¹âÆ×µÄÎüÊÕ·åÔÚʲôλÖÃ
ÒѾÓÐ8È˻ظ´
yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
- ºì»¨: 21
- Ìû×Ó: 2773
- ÔÚÏß: 261.2Сʱ
- ³æºÅ: 942922
- ×¢²á: 2010-01-15
- ÐÔ±ð: MM
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
shaoyan415: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ллÄú 2015-04-15 08:48:28
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
shaoyan415: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ллÄú 2015-04-15 08:48:28
|
1 . 21¦Â, 22¦Á-O-diangeloyl camelliagenin D C40H60O8 ÏàËÆ¶È:63.4% Phytochemistry 2002 59 825-832 Triterpenoid saponins and acylated prosapogenins from Harpullia austro-caledonica Laurence Voutquenne, C¨¦cile Kokougan, Catherine Lavaud,Isabelle Pouny, Marc Litaudon Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . caraganoside B C40H64O10 ÏàËÆ¶È:63.4% Journal of Chinese Pharmaceutical Sciences 1998 7 1-6 Two NewTriter penoids from the Roots of Caragana intermedia K. Wen-HanLin, Hong-Zheng Fu and Li-He Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . acetylilexolic acid methyl ester ÏàËÆ¶È:61.3% Archives of Pharmacal Research 1987 10 132-141 New triterpenoid saponins fromIlex pubescens Yong Nam Han, Seung Kyung Bail, Tae Hee Kim and Byung Hoon Han Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Olean-12-ene-3¦Â,15¦Á,16¦Á,28-tetrol-21-(2-methylbutanoic acid)-22-angelic acid C40H64O8 ÏàËÆ¶È:60.9% Phytochemical Analysis 1995 6 157-163 Prosapogenins from Dodonaea attenuata Andrew Y. T. Han, Leon Van Gorkom, Ian J. McFarlane and Kevin D. Barrow Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . Olean-12-ene-3¦Â,15¦Á,16¦Á,28-tetrol-21-(2-hydroxy-2-methyl-3-methoxybutanoic acid)-22-angelic acid C41H66O10 ÏàËÆ¶È:60.9% Phytochemical Analysis 1995 6 157-163 Prosapogenins from Dodonaea attenuata Andrew Y. T. Han, Leon Van Gorkom, Ian J. McFarlane and Kevin D. Barrow Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 3¦Â-hydroxy-22-oxo-12-oleanen-29-oic acid 3-O-¦Â-D-glucuronopyranosyl-6'-O-n-butyl ester C40H62O10 ÏàËÆ¶È:60.9% Journal of Natural Medicines 2012 66 Two new triterpenoid saponins from Caragana microphylla seeds Cheng-Jian Zheng • Gui-Lin Jin • Jing-Ping Zou •Yi-Ping Jiang • Pei-Xin Sun • Lu-Ping Qin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 3¦Â-hydroxy-22-oxo-12-oleanen-29-oic acid 3-O-¦Â-D-glucuronopyranosyl-6'-O-n-butyl ester C40H62O10 ÏàËÆ¶È:60.9% Journal of Natural Medicines 2013 67 190-195 Two new triterpenoid saponins from Caragana microphylla seeds Cheng-Jian Zheng, Gui-Lin Jin, Jing-Ping Zou, Yi-Ping Jiang¡ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . ilexpublesnin F C41H64O12 ÏàËÆ¶È:60.9% Planta Medica 2013 79 70-77 Ilexpublesnins C-M, Eleven New Triterpene Saponins from the Roots of Ilex pubescens Zhou, Yuan; Chai, Xing-Yun; Zeng, Ke-Wu; Zhang, Jia-Yu; Li, Ning; Jiang, Yong; Tu, Peng-Fei: Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 28-O-acetyl-3-O'-propargyloxycarbonylbetulin C36H54O5 ÏàËÆ¶È:60.9% Molecules 2013 18 4526-4543 Synthesis, Structure and Cytotoxic Activity of New Acetylenic Derivatives of Betulin Stanisław Boryczka, Ewa Bębenek, Joanna Wietrzyk, Katarzyna Kempi¨½ska, Maria Jastrzębska, Joachim Kusz and Maria Nowak Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 1¦Â-angeloyl-3¦Â,15¦Á,16¦Á,28-tetrahydroxy-22¦Á-(2-methylbutanoyloxy)-olean-12-en-23-al C40H62O9 ÏàËÆ¶È:60.9% Helvetica Chimica Acta 2013 96 1126-1133 Triterpenoids from the Roots of Camellia oleifera C.Abel and Their Cytotoxic Activities Shou-Li Wang, Zhong Chen, Xiao-Jing Tong, Yan-Li Liu, Xia Li, Qiong-Ming Xu, Xiao-Ran Li and Shi-Lin Yang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-04-14 10:51:31













»Ø¸´´ËÂ¥
10