| ²é¿´: 268 | »Ø¸´: 1 | |||
xianyunxiaгæ (³õÈëÎÄ̳)
|
[ÇóÖú]
άÆÕÇóÖú ÒÑÓÐ1È˲ÎÓë
|
|
39.39,39.60,39.81,40.02,40.22,40.43,40.64,42.56,49.07,78.86,95.61,96.39,102.39,114.60,114.80,115.24,115.85,118.37,122.68,126.87,129.66,130.00,137.62,145.46,145.67,146.18,156.83,159.25,162.97,163.33,163.98,172.49 DMSO лл£¡ |
» ²ÂÄãϲ»¶
288Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
¸´ÊÔµ÷¼Á
ÒѾÓÐ12È˻ظ´
¼ÆËã»ú11408£¬286·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁÏר˶322·Ö
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸ÉϺ£º£Ñó´óѧ083200ʳƷѧ˶£¬Çóµ÷¼Á£¬½ÓÊÜÆäËûרҵ083200
ÒѾÓÐ5È˻ظ´
081200-11408-276ѧ˶Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ10È˻ظ´
313Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
304Çóµ÷¼Á£¨085602£¬¹ýËļ¶£¬Ò»Ö¾Ô¸985£©
ÒѾÓÐ14È˻ظ´
²ÄÁϹ¤³Ì302·ÖÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
lb1527
½ð³æ (СÓÐÃûÆø)
- Ó¦Öú: 139 (¸ßÖÐÉú)
- ½ð±Ò: 851.4
- ºì»¨: 3
- Ìû×Ó: 211
- ÔÚÏß: 52.4Сʱ
- ³æºÅ: 2347914
- ×¢²á: 2013-03-15
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
1 . (S)-eriodictyol 7-O-(6''-O-trans-p-coumaroyl)-¦Â-D-glucopyranoside C30H28O13 ÏàËÆ¶È:53.1% Chemical & Pharmaceutical Bulletin 2002 50(6) 841-843 Two New Acylated Flavanone Glycosides from the Leaves and Branches of Phyllanthus emblica Ying-Jun ZHANG,Tomomi ABE,Takashi TANAKA,Chong-Ren YANG,and Isao KOUNO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . speranskoside ÏàËÆ¶È:50% Journal of Chinese Pharmaceutical Sciences 1997 6 07 Flavonoids from Speranskia Tuberculata Yan-Mei Li, Yu-Yin gZhao, Yun-Bai Fan, Xuan Wang and Li-Ning Cai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (2S)-2,3-dihydrorobustaflavone-4'-methyl ether C31H22O10 ÏàËÆ¶È:50% Journal of Asian Natural Products Research 2008 10 945-952 Four new biflavonoids from Selaginella uncinata and their anti-anoxic effect Jun-Xi Zheng, Nai-Li Wang, Hong-Wei Liu, Hai-Feng Chen, Ming-Ming Li, Li-Ying Wu,Ming Fan and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 2'',3''-dihydrophilonotisflavone ÏàËÆ¶È:50% Phytochemistry 1999 52 297-302 Biflavonoids and 4,20-epoxy-3-phenylcoumarins from the moss Mnium hornum Elke Brinkmeier, Hans Geiger, Hans Dietmar Zinsmeister Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 2,3-dihydrodicranolomin ÏàËÆ¶È:50% Phytochemistry 1995 40 573-576 The first biaurone, a triflavone and biflavonoids from two Aulacomnium species Hannelore Hahn, Tassilo Seeger, Hans Geiger, Hans Dietmar Zinsmeister, Kenneth R. Markham, Herbert Wong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . N-(1-(3-Bromophenylamino)-4-cyanoisoquinolin-7-yl)-1H-indol-2-carboxamide C25H16BrN5O ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 429-439 Synthesis and biological evaluation of 7-substituted-1-(3-bromophenylamino)isoquinoline-4-carbonitriles as inhibitors of myosin light chain kinase and epidermal growth factor receptor Haridas B. Rode, Martin L. Sos, Christian Gr¨¹tter, Stefanie Heynck, Jeffrey R. Simard, Daniel Rauh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . GB-2 ÏàËÆ¶È:50% Chinese Traditional and Herbal Drugs 2007 38 993-994 ÔÆÄÏɽÖñ×ÓÖ¦ÌõµÄ»¯Ñ§³É·ÖÑо¿ Éò½Ü;Ñî¾þɽ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . compound 2a ÏàËÆ¶È:50% Molecules 2012 17 6114-6125 Preussianone, a New Flavanone-Chromone Biflavonoid from Garcinia preussii Engl. Bernadette Biloa Messi, Karine Ndjoko-Ioset, Barbara Hertlein-Amslinger, Alain Meli Lannang, Augustin E. Nkengfack, Jean-Luc Wolfender, Kurt Hostettmann and Gerhard Bringmann Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-10-27 20:55:09














»Ø¸´´ËÂ¥