| ²é¿´: 266 | »Ø¸´: 1 | |||
fly5½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú 2g-6-3 ¼×´¼ ÒÑÓÐ1È˲ÎÓë
|
|
49.1,61.0,69.9,73.4,76.7,77.5,79.1,95.9,96.9,100.0,103.7,115.6,115.6,128.9,128.9,129.1,158.3,163.2,163.4,165.7,197.7 [ ·¢×ÔÊÖ»ú°æ http://muchong.com/3g ] |
» ²ÂÄãϲ»¶
327Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
08¹¤¿ÆÇóµ÷¼Á290·Ö
ÒѾÓÐ11È˻ظ´
Ò»Ö¾Ô¸985³õÊÔ354·ÖÉúÎïµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸2110£¬»¯Ñ§Ñ§Ë¶310·Ö£¬±¾¿ÆÖصãË«·ÇÇóµ÷¼Á
ÒѾÓÐ13È˻ظ´
353Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
308Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
334Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
Ò»Ö¾Ô¸0807 ÊýÒ»Ó¢Ò» 313 ÓÐûÓжþÂÖµ÷¼Á
ÒѾÓÐ7È˻ظ´
¸´ÊÔµ÷¼Á£¬Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤289·Ö
ÒѾÓÐ14È˻ظ´
086000µ÷¼Á
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×Êý¾ÝÇóÖú£¬Çë´ó¼Ò°ï棡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬¼±Çó£¬ds-3
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖúLF-106
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
80-6΢Æ×ÇóÖú2014.12.11
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¡¸Ð¼¤£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»~~
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ3È˻ظ´
¸÷λÐÂÄêºÃ ÇóÖú΢Æ× Éͽð80 ÒѾ°´ÕÕ΢Æ×¸ñʽÕûÀíºÃ ллÁË
ÒѾÓÐ7È˻ظ´
΢Æ×ÇóÖú3¸ö»¯ºÏÎï
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬ÔÚÏßµÈ
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖúÒ»»¯ºÏÎ£¡
ÒѾÓÐ5È˻ظ´
΢Æ×Êý¾Ý¡£Ç󻯺ÏÎï½âÎö
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´

cjpballack
Ìú¸Ëľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 328 (´óѧÉú)
- ½ð±Ò: 6551.4
- ºì»¨: 8
- Ìû×Ó: 663
- ÔÚÏß: 88.5Сʱ
- ³æºÅ: 2433043
- ×¢²á: 2013-04-23
- ÐÔ±ð: GG
- רҵ: ÖÐҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
fly5: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-06-19 13:58:34
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
fly5: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-06-19 13:58:34
|
²éѯ½á¹û£º¹²²éµ½275¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . Prunin ÏàËÆ¶È:95.2% Chemistry of Natural Compounds 1993 29 303-305 ACYLATED FLAVANONE GLYCOSIDES FROM Ricinus communis M. P. Yuldashev, E. Kh. Batirov, V. M. Malikov,and P. Kh. Yuldashev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . nalingenin 7-O-¦Â-D-glucopyranoside ÏàËÆ¶È:95.2% Korean Journal of Pharmacognosy 2002 33(4) 404-410 Phenolic Compounds from Barks of Ulmus macrocarpa and Its Antioxidative Activities Kwon, Young-Min; Lee, Jae-Hee; Lee, Min-Won Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . naringenin 7-O-¦Â-D-glucopyranoside ÏàËÆ¶È:95.2% Chemical & Pharmaceutical Bulletin 2006 54 435-441 Studies on the Constituents of Scutellaria Species (XXII). Constituents of the Roots of Scutellaria amabilis HARA Yukinori Miyaichi, Eiji Hanamitsu, Haruhisa Kizu and Tsuyoshi Tomimori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . pruning ÏàËÆ¶È:95.2% Chinese Journal of Natural Medicines 2004 2 59-61 Study on Flavonoids from Lysimachia clethroides ZOU Hai Yan; TU Peng Fei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (2S)-Naringenin-7-O-¦Â-D-glucopyranoside ÏàËÆ¶È:95.2% Chinese Journal of Natural Medicines 2009 7 357-360 Flavonones from Helichrysi flos syn. WANG Li-Bo; GAO Hui-Yuan; TOSHI Morikawa; SUN Bo-Hang; HUANG Jiang; MASAYUKI Yoshikawa; WU Li-Jun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . naringenin-7-O-glucoside ÏàËÆ¶È:95.2% Archives of Pharmacal Research 1990 13 374-378 Phytochemical study on Prunus davidiana Jae Sue Choi, Won Sick Woo, Han Suk Young and Jong Hee Park Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . naringenin-7-O-¦Â-D-glucopyranoside ÏàËÆ¶È:95.2% Journal of Shenyang Pharmaceutical University 2014 31 681-691 Isolation and identification of chemical constituents in roots and rhizomes of Asarum heterotropoides Fr.Schmidt var. mandshuricum(Maxim. )Kitag. QI Wen, WANG Li-li, WEN Hao, WANG Wei-ning, ZHANG Lin, YUAN Dan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . naringenin 7-O-glucoside ÏàËÆ¶È:90.4% Phytochemistry 2010 71 201-205 Biotransformation of naringin and naringenin by cultured Eucalyptus perriniana cells Kei Shimoda, Naoji Kubota, Koji Taniuchi, Daisuke Sato, Nobuyoshi Nakajima, Hatsuyuki Hamada, Hiroki Hamada Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . naringenin 4'-O-¦Â-D-glucopyranoside ÏàËÆ¶È:90.4% Phytochemistry 2010 71 201-205 Biotransformation of naringin and naringenin by cultured Eucalyptus perriniana cells Kei Shimoda, Naoji Kubota, Koji Taniuchi, Daisuke Sato, Nobuyoshi Nakajima, Hatsuyuki Hamada, Hiroki Hamada Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . èÖÆ¤ËØ-7-O-¦Â-D-ÆÏÌÑÌÇÜÕ ÏàËÆ¶È:90.4% China Journal of Chinese Materia Medica 2012 37 1402-1407 Chemical constituents of Phymatopteris hastate and their antioxidant activity DUAN Shilian; TANG Sheng¡äan; QIN Nan; DUAN Hongquan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-06-19 13:26:28













»Ø¸´´ËÂ¥