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PSA: ½ð±Ò+2, 3u 2013-06-14 13:41:57
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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£º¹²²éµ½160¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . esculetin C9H6O4 ÏàËÆ¶È:66.6% Chinese Traditional and Herbal Drugs 2009 40 1036-1039 ŵÀöÇà¹û»¯Ñ§³É·ÖÑо¿ ÌÀ½¨¹ú;Èθ£²Å;Áõ¼ª¿ª Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . esculetin C9H6O4 ÏàËÆ¶È:66.6% Natural Product Research and Development 2009 21 779-781 Chemical Constituents of Morinda cltrifolia TANG Jian-guo;REN Fu-cai; LIU Ji-kai Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ferulic acid ÏàËÆ¶È:66.6% Chinese Traditional and Herbal Drugs 2011 42 440-442 Chemical constituets of Sparganium stoloniferum KONG Li-juan, LIANG Qiao-li, WU Qi-nan, JIANG Ji-hong Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ferulic acid ÏàËÆ¶È:66.6% Chinese Pharmaceutical Journal 2012 47 1987-1989 Chemical Constituents of Scirpus yagara Ohwi CUI Xiao-dong; LIANG Qiao-li; KONG Li-juan; WU Qi-nan; GU Wei; DUAN Jin-ao Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . scopoletin C10H8O4 ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 2009 40 1036-1039 ŵÀöÇà¹û»¯Ñ§³É·ÖÑо¿ ÌÀ½¨¹ú;Èθ£²Å;Áõ¼ª¿ª Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 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Miranda, Lise-Lotte Gundersen Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . scopoletin ÏàËÆ¶È:60% Natural Product Research and Development 2008 20 765-769 Studies on the Chemical Constituents of the Fruit of Acanthopanax sessiliflorus(Rupr.et Maxim.) Seem. AN Qi; YANG Chun-juan; SONG Yang; YU Kai; XIONG Zhi-li; LI Fa-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . scopoletin C10H8O4 ÏàËÆ¶È:60% Chinese Journal of Natural Medicines 2011 9 115-119 Chemical Constituents of Toona ciliata var. pubescens LIU Yu-Bo, CHENG Xiang-Rong, QIN Jiang-Jiang, YAN Shi-Kai, JIN Hui-Zi *, ZHANG Wei-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 6-methoxy-7-hydroxycoumarin ÏàËÆ¶È:55.5% Journal of Chinese Pharmaceutical Sciences 2003 12 181-183 A Monoterpene G lycoside from Ehinacea purpurea LI Ji-ren , BAI Yan-jing , WANGBin , CHEN Gang , AI Tie-min , and ZHAO Yu-ying Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . aeculetin ÏàËÆ¶È:55.5% China Journal of Chinese Materia Medica 2007 32 1132-1134 Studies on Chemical Constituents of Lonicera syringantha Maxim QIAN Zhengming, LI Huijun, QI Fangfan, HE Qinghui, LI Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 6,7-dihydroxycoumarin ÏàËÆ¶È:55.5% China Journal of Chinese Materia Medica 2006 31 1694-1696 Studies on chemical constituents of Euphorbia sororia ZHANG Weiku, YANG Guoen, LI Qian, ZHANG Xiaoqi, YE Wencai Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . esculin ÏàËÆ¶È:55.5% China Journal of Chinese Materia Medica 2002 27 199-201 Chemical Constituents from Alyxia sinensis WANG Gangli, YAN Hua, HOU Qingyun, LU Yang, GONG Ningbo, LIN Ruichao Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . esculetin C9H6O4 ÏàËÆ¶È:55.5% Acta Pharmaceutica Sinica 2002 Vol 37 535-538 STUDIES ON THE PHENOLIC ACID CONSTITUENTS FROM CHINESE MEDICINE ¡°SHENG-MA¡±,RHIZOME OF CIMICIFUGA FOETIDA L. ZHAO Xiao-hong; CHEN Di-hua; SI Jian-yong; PAN Rui-le; SHEN Lian-gang Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . umbelliferone ÏàËÆ¶È:55.5% Natural Product Sciences 2005 11 79-84 Coumarins and Chromones from Angelica genuflexa An, Ren-Bo; Park, Bo-Young; Kim, Jung-Hee; Kwon, Ok-Kyoung; Lee, Joong-Ku; Min, Byung-Sun; Ahn, Kyung-Seop; Oh, Sei-Ryang; Lee, Hyeong-Kyu Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . scopoletin ÏàËÆ¶È:55.5% Korean Journal of Pharmacognosy 2004 35(1) 80-87 The Chemical Structures and Their Antioxidant Activity of the Components Isolated from the Heartwood of Hemiptelea davidii Chang, Bok-Sim; Kwon, Yong-Soo; Kim, Chang-Min Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . ÆßÒ¶ÄÚõ¥(esculetinon) C9H6O4 ÏàËÆ¶È:55.5% Chinese Journal of Marine Drugs 2006 25(3) 15-17 Study on the chemical constituents of Ipomoea Pescaprae( L.) Sweet(I) WANG Qing-Ji, WANG You-Shao, HE Lei, ZHANG Si Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 2',3'-dioxygenated flavone ÏàËÆ¶È:55.5% Phytochemistry 1989 28 681-694 Natural occurrence and synthesis of 2'-oxygenated flavones,flavonols,flavanones and chalcones Munekazu Iinuma,Mizuo Mizuno Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 6,7-difluoro-4-hydroxyquinolin-2(1H)-one C9H5F2NO2 ÏàËÆ¶È:55.5% Journal of Heterocyclic Chemistry 2003 40 617-623 Synthesis and biological properties of 4-substituted quinolin-2(1H)-one analogues Jae-Chul Jung,Seikwan Oh,Won-Ki Kim,Woo-Kyu Park,Jae Yang Kong and Oee-Sook Park Structure 13C NMR ̼Æ×Ä£Äâͼ |

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