| ²é¿´: 514 | »Ø¸´: 1 | |||
ËÉÂÜ·çľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú F832 13C-NMR(DMSO-d6)·Ç³£¸Ðл£¡ ÒÑÓÐ1È˲ÎÓë
|
|
F832 13C-NMR(DMSO-d6) 59.9,94.4,104.2,104.6,126.3,129.1,130.8,131.6,131.9,152.6,152.7,158.0,163.1,182.2 |
» ²ÂÄãϲ»¶
335Çóµ÷¼Á
ÒѾÓÐ23È˻ظ´
279Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
322Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
271Çóµ÷¼Á
ÒѾÓÐ39È˻ظ´
Ò»Ö¾Ô¸Öпƴó²ÄÁÏÓ뻯¹¤£¬353·Ö»¹Óе÷¼ÁѧУÂð
ÒѾÓÐ10È˻ظ´
294Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
ÊÕµ½¸´ÊÔµ÷¼Áµ«ÊÇÈ¥²»ÁË
ÒѾÓÐ6È˻ظ´
ÓÐûÓнÓÊձȽϿìµÄsciÆÚ¿¯Ñ½£¬×îºÃÔÚÒ»¸öÔÂÖ®Äڵģ¬ÑÐÈýº¢×ÓÇó±ÏÒµ
ÒѾÓÐ5È˻ظ´
¿ÒÇëÓÐѧУÊÕÁô
ÒѾÓÐ8È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¡¸Ð¼¤£¡
ÒѾÓÐ3È˻ظ´
·Ç³£¸Ðл£¡Î¢Æ×ÇóÖú
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Íò·Ö¸Ðл~
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ3È˻ظ´
¸÷λÐÂÄêºÃ ÇóÖú΢Æ× Éͽð80 ÒѾ°´ÕÕ΢Æ×¸ñʽÕûÀíºÃ ллÁË
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
¼±Çó΢Æ×¿â²éѯ£¡·Ç³£¸Ðл£¡
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48453.9
- ºì»¨: 52
- Ìû×Ó: 6753
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ËÉÂÜ·ç: ½ð±Ò+8 2015-05-19 12:21:33
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ËÉÂÜ·ç: ½ð±Ò+8 2015-05-19 12:21:33
|
1 . Oroxylin A ÏàËÆ¶È:100% Fitoterapia 2010 81 552-556 Flavonoids with prolyl oligopeptidase inhibitory activity isolated from Scutellaria racemosa Pers Micaela R. Marques, Caroline St¨¹ker, Nessim Kichik, Teresa Tarrag¨®, Ernest Giralt, Ademir F. Morel, Ionara I. Dalcol Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . oroxylin-A ÏàËÆ¶È:100% Chinese Journal of Medicinal Chemistry 2009 19 59-62 Chemical constituents from Scutellaria baicalensis Georgi LIU Ying-xue, LIU Zhong-gang, SU Lan, YANG Rui-ping, HAO Dong-fang, PEI Yue-hu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . oroxylin A ÏàËÆ¶È:100% Natural Product Research and Development 2010 22 949-951 Cytotoxic Constituents from the Root of Ardisia crispa HUANG Wei; TAN Gui-shan;XU Kang-ping; LI Fu-shuang; LI Zhong-kui; LIU Yan-ping Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . negletein CI6H12O5 ÏàËÆ¶È:87.5% Journal of Natural Products 1985 Vol 48 819-822 Flavonoids from Centaurea clementei I. Gonzalez Collado, F. A. Macias, G. M. Massanet, F. Rodriguez Luis Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . oroxylin A ÏàËÆ¶È:87.5% Journal of Shenyang Pharmaceutical University 2003 20 181-183 Isolation and identif ication of the chemical constituents of roots of Scutellaria amoena C. H. Wright XIAO Li-he, WANG Hong-yan, SONG Shao-jiang, ZHANG Guang-ping, SONG Hai-xiu, XU Sui-xu Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . oroxylin A ÏàËÆ¶È:87.5% Journal of Shenyang Pharmaceutical University 2003 20 339-348 Studies on chemical constituents of the roots of Scutellaria viscidula Bge. WANG Hong-yan, XIAO Li-he, LIU Li, XU Sui-xu Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . baicalein-6-methyl ether ÏàËÆ¶È:87.5% Chemistry & Biodiversity 2012 9 2096-2158 Flavonoids in Subtribe Centaureinae (Cass.) Dumort. (Tribe Cardueae, Asteraceae): Distribution and 13C-NMR Spectral Data Carmen Formisano, Daniela Rigano, Felice Senatore, Svetlana Bancheva, Antonella Maggio, Sergio Rosselli and Maurizio Bruno Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . wogonin C16H12O5 ÏàËÆ¶È:87.5% Phytochemistry Letters 2014 8 213-219 Bioactivity-guided isolation of antiproliferative compounds from Centaurea carduiformis DC Ayse Sahin Yaglioglu, Ibrahim Demirtas, Nezhun Goren Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-05-19 11:53:32













»Ø¸´´ËÂ¥