| ²é¿´: 339 | »Ø¸´: 1 | ||
·çÉñzg121ľ³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
½á¹¹½âÎö ÏàËÆ¶Èǰ10 ÒÑÓÐ1È˲ÎÓë
|
|
CÆ×Êý¾Ý£º40.24,48.79,93.53,98.36,103.19,115.23,115.78,120.15,122.13,135.92,145.24,146.98,147.89,156.31,160.91,164.06,176.03 ÈܼÁ£ºDMSO |
» ²ÂÄãϲ»¶
²ÄÁÏרҵ344Çóµ÷¼Á
ÒѾÓÐ19È˻ظ´
085404 298·ÖÇóµ÷¼Á
ÒѾÓÐ11È˻ظ´
296Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
³õÊÔ261
ÒѾÓÐ6È˻ظ´
284Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
²ÄÁÏ085601µ÷¼Á
ÒѾÓÐ25È˻ظ´
272·Ö²ÄÁÏ×ÓÇóµ÷¼Á
ÒѾÓÐ23È˻ظ´
22408µ÷¼ÁÇóÖú
ÒѾÓÐ7È˻ظ´
µ÷¼Á
ÒѾÓÐ17È˻ظ´
²ÄÁÏÀà284µ÷¼Á
ÒѾÓÐ43È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
¸÷λ´óÉñ£¬°ïæ¿´Ò»ÏÂÕâ¸öÆ×
ÒѾÓÐ4È˻ظ´
GC-MS²â¶¨Ò»ÀàÎïÖÊ£¿
ÒѾÓÐ8È˻ظ´
ÇóÒ»¸ö»¯ºÏÎïµÄcÆ×Êý¾ÝÆ¥Åä
ÒѾÓÐ7È˻ظ´
ÈçºÎ·ÖÎö¸ß¾ÛÎïÖеijɷ֣¿
ÒѾÓÐ16È˻ظ´
µÚÒ»´ÎͶ¸å£¬Éó¸å½áÊø±à¼ËµÏàËÆ¶È¸ß£¬Çó´óÉñÖ¸µã
ÒѾÓÐ11È˻ظ´
΢Æ×ÇóÖú £¡£¡£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬ÌṩÏàËÆ¶È¿¿Ç°µÄ5ƪÎÄÏ×£¬Ð»Ð»
ÒѾÓÐ10È˻ظ´
GC-MS·ÖÎö£¬³ö·åʱ¼ä²»Í¬£¬m/zÏàͬ£¬´ú±íµÄÊDz»Í¬ÎïÖÊÂð£¿
ÒѾÓÐ21È˻ظ´
Á½¸öÆ×£¬¸÷ÐèÒªÏàËÆ¶Èǰ10µÄ£¬Ð»Ð»¡£
ÒѾÓÐ3È˻ظ´
GC-MS²â»Ó·¢ÐԳɷÖʱÏàËÆ¶ÈµÍµÄÔõô°ì£¿
ÒѾÓÐ5È˻ظ´
¾Û½¹ÉúÎï·ÂÖÆÒ©ÏµÁÐ
ÒѾÓÐ6È˻ظ´
ÇóÖúÖ»ÓÐ3¸ö̼µÄ»¯ºÏÎ
ÒѾÓÐ3È˻ظ´
ÇóÖúºìÍâ½âÎöÈí¼þ
ÒѾÓÐ11È˻ظ´
ºìÍâÄܹ»È·¶¨ÊÇ·ñÊÇZSM-5½á¹¹Â
ÒѾÓÐ11È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
[ÇóÖú¡¿ÊýÖµ·½·¨²»Í¬£¬µ«½á¹û·ÖÎö·½·¨ÀàËÆ£¬Ëã²»ËãÏàËÆ»ò³Ï®¡£
ÒѾÓÐ3È˻ظ´
ͬԴ콍£¬Ä£°åÈçºÎÑ¡Ôñ
ÒѾÓÐ3È˻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 ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
·çÉñzg121(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+10 2015-05-06 13:16:58
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
·çÉñzg121(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+10 2015-05-06 13:16:58
|
²éѯ½á¹û£º¹²²éµ½985¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . quercetin C15H10O7 ÏàËÆ¶È:88.2% Acta Botanica Yunnanica 2001 23(3) 352-356 The Chemical Constituents of Parakmeria yunnanensis CHENG Yong-Xian,ZHOU Jun, TAN Ning-Hua Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . quercetin ÏàËÆ¶È:88.2% Acta Botanica Yunnanica 2000 22(3) 343-350 Chemical Constituents of Crude Green Tea ,the Material of Pu - er Tea in Yunnan ZHOU Zhi-Hong,YANG Chong-Ren Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Quercetin C15H10O7 ÏàËÆ¶È:88.2% Acta Botanica Yunnanica 2000 22(1) 90-96 Saluenin , a New Flavonol Glycoside from Camellia saluenensis ZHOU Zhi-Hong,ZHANG Ying-Jun,YANG Chong-Ren Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . quercetin ÏàËÆ¶È:88.2% Chemical & Pharmaceutical Bulletin 1988 36 1180-1184 Chemical Studies on the COnstituents of Hyphear Tanakae HOSOKAWA from Different Host Trees TAKEHIKO FUKUNAGA,KOICHI NISHIYA,IKUKO KAJIKAWA,YOSHIKUNI WATANABE,NOBUO SUZUKI,KOICHI TAKEYA and HIDEJI ITOKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Quercetin ÏàËÆ¶È:88.2% Chemistry of Natural Compounds 2008 44 370-371 FLAVONOIDS FROM Gossypium hirsutum FLOWERS T. Wu, R. Abdulla,Y. Yang, and H. A. Aisa Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 1,3,6-cycloheptatrien-3,4,6-trihydroxy-5-oxo-1-carboxylic ÏàËÆ¶È:88.2% Chemistry of Natural Compounds 2006 42 148-151 PHENOLIC COMPOUNDS FROM Filipendula ulmaria E. A. Krasnov, V. A. Raldugin,I. V. Shilova and E. Yu. Avdeeva Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . quercetin ÏàËÆ¶È:88.2% Acta Botanica Sinica 1997 39 82-84 A New Diterpenoid from Alpinia zerumbet Wen Yuan-ying, Chen Yan-fang and Xie Xue-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3-Methoxyquercetin C15H10O7 ÏàËÆ¶È:88.2% Molecules 2007 12 2130-2139 Acetylcholinesterase Inhibition by Flavonoids from Agrimonia pilosa Mankil Jung and Moonso Park Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Quercetin C15H10O7 ÏàËÆ¶È:88.2% Molecules 2007 12 2130-2139 Acetylcholinesterase Inhibition by Flavonoids from Agrimonia pilosa Mankil Jung and Moonso Park Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Quercetin C15H10O7 ÏàËÆ¶È:88.2% Molecules 2008 13 1931-1941 Flavonoids and a New Polyacetylene from Bidens parviflora Willd Yu-Lan Li, Jun Li, Nai-Li Wang and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Quercetin C15H10O7 ÏàËÆ¶È:88.2% Molecules 2008 13 2796-2803 A New Phloroglucinol Diglycoside Derivative from Hypericum japonicum Thunb. Xiao W. Wang, Yu Mao, Nai-Li Wang and Xin S. Yao Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-04-30 13:36:36













»Ø¸´´ËÂ¥