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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½1225¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 7,3'-Dihydroxy-40-methoxyflavone-7-O-¦Â-glucopyranoside C22H22O10 ÏàËÆ¶È:68.1% Biochemical Systematics and Ecology 2007 35 274-280 Chemical constituents of the seeds of Ammopiptanthus (Leguminosae) and their systematic and ecological significance Huanhuan Wei, Ping Wu, Xuejun Ge, Meifang Liu, Xiaoyi Wei Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . linaroside ÏàËÆ¶È:66.6% Journal of Natural Products 2000 63 765-767 Nematicidal Constituents of the Aerial Parts of Lantana camara Sabira Begum,Aneela Wahab, Bina S. Siddiqui, and Fatima Qamar Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 7-O-glucoluteolin ÏàËÆ¶È:66.6% Acta Pharmaceutica Sinica 1998 Vol 33 591-596 STUDIES ON THE CHEMICAL CONSTITUENTS OF THE LEAVES FROM ARTABOTRYS HEXAPETALUS Li Tongmei(Li TM) and Yu Jingguang(Yu JG)ª¤ Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . luteolin 7-O-¦Â-glucopyranoside ÏàËÆ¶È:66.6% Natural Product Sciences 1998 4 153-157 Chemical Investigation of the Constitutive Phenolics of Ailanthus altissima; The Structure of a New Flavone Glycoside Gallate Barakat, Heba H. Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Pectolinarigenin-7-O-¦Â-D-glucopyranoside ÏàËÆ¶È:66.6% Archives of Pharmacal Research 1994 17 487-489 Determination of the structure for polysubstituted flavonoid and 6-C-glucosyl flavonoids using13C-1H long range couplings Min-Won Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Pectolinarigenin 7-O-¦Â-D-glucopyranoside ÏàËÆ¶È:66.6% Archives of Pharmacal Research 2003 26 128-131 A polyacetylene and flavonoids from cirsium rhinoceros Yim Soon-Ho, Kim Hyun Jung and Lee Ik-Soo Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . luteolin-7-¦Â-O-glucoside ÏàËÆ¶È:66.6% Zeitschrift f¨¹r Naturforschung C 2003 58 347-350 A New Highly Oxygenated Flavone from Vernonia saligna Y. Huang, Z.-H. Ding, and J.-K. Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . diosmetin-7-O-¦Â-D-glucoside ÏàËÆ¶È:66.6% Chemistry and Industry of Forest Products 2006 26 6-8 Flavonoids from the Aerial Parts of Lonicera syringantha Maxim. QIAN Zheng-ming, LI Hui-jun, QI Fang-fang, HE Qing-hui, LI Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ľϬ²ÝËØ7-O-¦Â-D-ÆÏÌÑÌÇÜÕ ÏàËÆ¶È:66.6% Journal of Chinese Medicinal Materials 2008 31 374-376 Study on Chemical Constituents Isolated from Juncus effuses SHAN Cheng-ying, YE Yong-hao, JIANG Hong-fang, ZHANG Jiu Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . diosmetin 7-O-¦Â-D-glucopyranoside ÏàËÆ¶È:63.6% China Journal of Chinese Materia Medica 2009 34 2761-2764 Chemical constituents of Galium verum ZHAO Chunchao, SHAO Jianhua, CAO Dandan, ZHANG Yuwei LIXian Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Ó¡¶È¾£½æÜÕ£¨nepitrin) ÏàËÆ¶È:63.6% Chinese Traditional and Herbal Drugs 2011 42(5) 859-862 Chemical constituents of Salvia plebaia LU Ru-mei, YANG Chang-shui, WEI Jian-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . nepitrin ÏàËÆ¶È:63.6% Chinese Journal of Natural Medicines 2007 5 421-424 Chemical Constituents of the Aerial Parts of Blumea riparia ZHENG Dan; ZHANG Xiao-Qi; WANG Ying; YE Wen-Cai Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . nepitrin ÏàËÆ¶È:63.6% Chinese Pharmaceutical Journal 2008 43 813-815 Study on Flavanoids from Salvia plebeia XIANG Lan, CHEN Hu-ning, XU Cheng-ming, ZHANG Shan-shan, WANG Hua-yan Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . diosmetin-7-O-¦Â-D-glucopyranoside ÏàËÆ¶È:63.6% Journal of Shenyang Pharmaceutical University 2010 27 34-36 Isolation and identification of flavonoidal constituents from the leaves of Lonicera japonica Thunb. MA Jun-li, LI Ning, LI Xian Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3'-O-methyl-3,4-methylenedioxyellagic acid 4'-O-¦Â-D-glucopyranoside ÏàËÆ¶È:63.6% Magnetic Resonance in Chemistry 1999 37 856-859 NMR assignments of ellagic acid derivatives Xing-Cong Li, Hala N. Elsohly, Charles D. Hufford and Alice M. Clark Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . diosmetin-7-O-¦Â-D-glucopyranoside ÏàËÆ¶È:63.6% Journal of Chinese Medicinal Materials 2009 32 1532-1534 Studies on Flavones from Flos Chrysanthemi Indici TANG Yi, GAO Mei-hua, YAO Mei-cun Structure 13C NMR ̼Æ×Ä£Äâͼ |

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