| ²é¿´: 261 | »Ø¸´: 1 | |||
libinoookľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ýwm-d-4-2-8 ÒÑÓÐ1È˲ÎÓë
|
| 13C NMR (126 MHz, pyridine) ¦Ä55.66,56.36,56.48,92.24,97.70,104.55,105.59,112.00,117.61,142.20,147.60,153.80,156.88,163.90,166.44,181.31 |
» ²ÂÄãϲ»¶
²ÄÁϹ¤³Ì085601£¬270Çóµ÷¼Á
ÒѾÓÐ24È˻ظ´
085404 293Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
µ÷¼Á
ÒѾÓÐ21È˻ظ´
¸´ÊÔµ÷¼Á£¬Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤289·Ö
ÒѾÓÐ15È˻ظ´
08¹¤¿ÆÇóµ÷¼Á290·Ö
ÒѾÓÐ12È˻ظ´
286Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
²ÄÁÏÀà284µ÷¼Á
ÒѾÓÐ24È˻ظ´
¿¼Ñе÷¼Á-²ÄÁÏÀà-284
ÒѾÓÐ14È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
Ò»Ö¾Ô¸985³õÊÔ354·ÖÉúÎïµ÷¼Á
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
podÊý¾Ý´¦ÀíÇóÖú
ÒѾÓÐ12È˻ظ´
Ò»¸ö¼òµ¥»¯ºÏÎïµÄ΢Æ×£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾ÝÒ»¸ö!
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý4¸ö
ÒѾÓÐ6È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý YC-8
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý1¸ö
ÒѾÓÐ6È˻ظ´
Çó΢Æ×£¬²»Ê¤¸Ð¼¤ÌéÁã
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúάÆ×Êý¾Ý¿â
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿°ïæ²éһϽ£Çž§Ì壨CCD£©Êý¾Ý¿â
ÒѾÓÐ7È˻ظ´
Ц¶à»á»³ÔÐ
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1216 (½²Ê¦)
- ½ð±Ò: 9788.1
- É¢½ð: 610
- ºì»¨: 40
- ɳ·¢: 3
- Ìû×Ó: 2723
- ÔÚÏß: 1284.6Сʱ
- ³æºÅ: 2010893
- ×¢²á: 2012-09-18
- ÐÔ±ð: GG
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
libinoook: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-06-07 10:24:16
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
libinoook: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-06-07 10:24:16
|
²éѯ½á¹û£º¹²²éµ½66¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 1-hydroxyl-3,5,8-trimethoxyxanthone ÏàËÆ¶È:93.7% Chinese Journal of Natural Medicines 2010 8 425-428 Chemical Constituents of Gentianella azurea SHI Ke-Li; WANG Ye-Qing; JIANG Qian; LIAO Zhi-Xin Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 1-hydroxy-3,5,8-trimethoxyxanthone ÏàËÆ¶È:93.7% Indian Journal of Chemistry Section B 1994 33B 405-408 (-)-Syringaresinol,a heptatoprotective agent and other constituents from Swertia chirata Ajit Kumar Chakravarty, Sibarata Moitra & Binayak Das Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 1-hydroxyl-3,5,8-trimethoxyxanthone ÏàËÆ¶È:87.5% Chinese Traditional and Herbal Drugs 2013 44 942-949 Chemical constituents from Swertia mussotii LUO Cui-ting, MAO Shuang-shuang, CHEN He-ru, LI Yu-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 1,6-dihydroxy-3,7-dimethoxyxanthone ÏàËÆ¶È:75% Chemical & Pharmaceutical Bulletin 1994 42 2305-2308 Xanthone C-Glycoside and Acylated Sugar from Polygala tenuifolia Yukinobu IKEYA,Ko SUGAMA and Masao MARUNO Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 1,6-dihydroxy-3,7-dimethoxyxanthone C15H12O6 ÏàËÆ¶È:75% Phytochemistry 1991 30 2061-2065 Two xanthones from Polygala tenuifolia Yukinobu Ikeya, Kô Sugama, Minoru Okada, Hiroshi Mitsuhashi Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . luteolin-7,4'-dimethyl ÏàËÆ¶È:70.5% Chemistry and Industry of Forest Products 2008 28 1-5 Antitumor Constituents from the Leaves of Aquilaria sinensis (Lour.) Gilg WANG Hong-gang, ZHOU Min-hua, LU Jing-jing, YU Bo-yang Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 1,3-dihydroxy-5,8-dimethoxyxanthone C15H12O6 ÏàËÆ¶È:68.7% Journal of Natural Products 1990 Vol 53 1463 Synthesis of Minor Xanthones from Garcinia mangostana Graham. J. Bennett, Hiok-Huang Lee, Liak-Phong Lee Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-06-07 09:59:26













»Ø¸´´ËÂ¥