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719660960(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+10 2015-05-09 12:17:23
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719660960(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+10 2015-05-09 12:17:23
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1 . oroxin B ÏàËÆ¶È:74.0% China Journal of Chinese Materia Medica 2013 38 204-207 Chemical constitunents of seeds of Oroxylum indicum WEI Xiao-nan, LIN Bin-bin, XIE Guo-yong, LI Jian-wen, QIN Min-jian Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . baicalein-7-O-diglucoside ÏàËÆ¶È:74.0% Journal of Separation Science 2010 33 1058-1063 Preparative isolation of flavonoid compounds from Oroxylum indicum by high-speed counter-current chromatography by using ionic liquids as the modifier of two-phase solvent system Renmin Liu, Lili Xu, Aifeng Li and Ailing Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Oroxin B ÏàËÆ¶È:74.0% Natural Product Research and Development 2013 25 628-630 Study on Chemical Constituents from Oroxylum indicum (L.) Vent. ZHANG Chang-zhuang, JIN Yin-hua, TONG Ya-nan, WANG Zhe, JIN Yong-ri, LI Xu-wen, YANG Zong-hui Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . baicalein-7-O-diglucoside ÏàËÆ¶È:74.0% Chromatographia 2008 68 885-892 Separation of Flavonoids from the Leaves of Oroxylum indicum by HSCCC Yuan Yuan, Wenli Hou, Minhai Tang, Houding Luo, Li-Juan Chen, Y. Hugh Guan, Ian A. Sutherland Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Baicalein 7-O-¦Â-D-glucuronopyranosyl-(1¡ú3)[¦Â-D-glucopyranosyl-(1¡ú6)]-¦Â-D-glucopyranoside C33H38O21 ÏàËÆ¶È:70.9% Fitoterapia 2011 82 841-848 Antioxidant flavonoids from the seed of Oroxylum indicum Ren-yi Yan, Yang-yang Cao, Cheng-yu Chen, Hui-qing Dai, Sheng-xian Yu, Jie-lin Wei, Hua Li, Bin Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . »ÆÜËÜÕÔª-7-O-¦Â-Áúµ¨¶þÌÇÜÕ ÏàËÆ¶È:70.3% Chinese Traditional and Herbal Drugs 2007 38 186-187 ľºûµû»¯Ñ§³É·ÖµÄÑо¿ ³ÂÁÁÁÁ;ËÎÏþ¿;ºîÎıò;ÕÅÐÂöÎ Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . schachristanoside C26H28O13 ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 2011 Vol. 47, No. 4 547-549 A NEW FLAVONE GLYCOSIDE FROM THE AERIAL PART OF Scutellaria schachristanica Z. O. Tashmatov, K. A. Eshbakova,and Kh. M. Bobakulov Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Wogonin-7-O-glcUA Me ester ÏàËÆ¶È:66.6% Journal of Shenyang Pharmaceutical University 2003 20 101-103 Study on the chemical constituents of the fruits of Forsythia suspensa(Thunb.) Vahl LIU Yue, SONG Shao-jiang, XU Sui-xu, FU Xiao-hui Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . baicalein 6-methyl ether 7-O-¦Â-galactopyranouronide ÏàËÆ¶È:66.6% 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 10 . 7-O-¦Â-D-Glucopyranosyl-4'-methylapigenin C22H22O10 ÏàËÆ¶È:66.6% 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 11 . Chrysin 6-C-¦Â-D-glucopyranosyl-8-O-¦Â-D-glucuronopyranoside C27H28O15 ÏàËÆ¶È:66.6% Fitoterapia 2011 82 841-848 Antioxidant flavonoids from the seed of Oroxylum indicum Ren-yi Yan, Yang-yang Cao, Cheng-yu Chen, Hui-qing Dai, Sheng-xian Yu, Jie-lin Wei, Hua Li, Bin Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . baicalein 7-(6''-O-malonylglucoside) ÏàËÆ¶È:62.9% Phytochemistry 1993 34 167-170 Additional flavonoids from elicitor-treated cell cultures of Cephalocereus senilis Liu Qin, Richard A. Dixon, Tom J. Mabry Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Scutellarein 7-O-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside C27H31O16 ÏàËÆ¶È:62.9% Fitoterapia 2011 82 841-848 Antioxidant flavonoids from the seed of Oroxylum indicum Ren-yi Yan, Yang-yang Cao, Cheng-yu Chen, Hui-qing Dai, Sheng-xian Yu, Jie-lin Wei, Hua Li, Bin Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Artemisidin A C27H30O18 ÏàËÆ¶È:62.9% Bioorganic & Medicinal Chemistry 2001 9 77-83 New constituents and antiplatelet aggregation and anti-HIV principles of Artemisia capillaris Tian-Shung Wu, Zhih-Jing Tsang, Pei-Lin Wu, Fu-Wen Lin, Chia-Yin Li, Che-Ming Teng, Kuo-Hsiung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 6-hydroxyapigenin-7-O-¦Â-[2-O-¦Â-xyloglucoside] ÏàËÆ¶È:62.9% Phytochemistry 2001 56 453-461 Flavonoid characters contributing to the taxonomic revision of the Hebe parviflora complex Kevin A. Mitchell, Kenneth R. Markham, Michael J. Bayly Structure 13C NMR ̼Æ×Ä£Äâͼ |

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