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kaola0916
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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 61.8,70.7,74.2,77.3,77.5,101.6,103.3,106.3,107.6,115.8,125.9,128.2,129.3,129.6,140.7,157.7,158.8,159.8 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½765¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . piceid C20H22O8 ÏàËÆ¶È:100% Phytochemistry 1996 42 1591-1593 Trans-resveratrol-3-O-¦Â-glucoside (piceid) in cell suspension cultures of vitis vinifera Pierre Waffo Teguo, Alain Decendit, Joseph Vercauteren, G¨¦rard Deffieux, Jean-Michel M¨¦rillon Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . polydotin peceid ÏàËÆ¶È:100% Acta Pharmaceutica Sinica 2005 Vol 40 1131-1134 A new stilbene glycoside from Dryopteris sublaeta FENG Wei-sheng CAO Xin-wei KUANG Hai-xue ZHENG Xiao-ke Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Piceid ÏàËÆ¶È:100% Archives of Pharmacal Research 2008 31 598-605 Lipoxygenase inhibitory constituents from rhubarb Tran Minh Ngoc, Pham Thi Hong Minh, Tran Manh Hung, Phuong Thien Thuong and IkSoo Lee, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . piceid C20H22O8 ÏàËÆ¶È:94.4% Chinese Traditional and Herbal Drugs 2009 40 1700-1703 ÝÃÝÖÖлÆÍªºÍ¶þ±½ÒÒÏ©Àà³É·ÖµÄÑо¿ ÉÛ²¨;¹ùºé×£;¹ûµÂ°² Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . piceid ÏàËÆ¶È:90% China Journal of Chinese Materia Medica 2009 34 1672-1675 Chemical constituents from roots of Incarvillea mairei HUANG Zhengsheng, ZHANG Weidong, LIN Sheng, LIU Chunmei, HUANG Dasen, SONG Taifa, LU Longhai, PEI Yuehu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (E)-Resveratrol-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:90% Archives of Pharmacal Research 2007 30 1471-1475 Two new phenolic constituents ofHumulus japonicus and their cytotoxicity testIn Vitro Byung Chul Yu, Min Cheol Yang, Kyu Ha Lee, Ki Hyun Kim and Sang Un Choi, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Piceid ÏàËÆ¶È:90% Archives of Pharmacal Research 2010 33 1331-1338 Inhibition of melanogenesis by piceid isolated from Polygonum cuspidatum Eui Taek Jeong, Mu Hyun Jin, Mi-Sun Kim, Yun Hee Chang and Sun Gyoo Park Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . resveratrol-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:90% Natural Product Research and Development 2008 20 257-261 Chemical Constituents of Keteleeria evelyniana FU Zhao-hui;ZHANG Yu-mei; TAN Ning-hua; CHU Hong-biao; JI Chang-jiu; Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 5-O-methyl-(E)-resveratrol 3-O-¦Â-D-glucopyranoside C21H24O8 ÏàËÆ¶È:89.4% Journal of Natural Products 2005 68 101-103 Two New Hepatoprotective Stilbene Glycosides from Acer mono Leaves Hyekyung Yang, Sang Hyun Sung, and Young Choong Kim Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (E)-resveratrol-3-O-¦Â-D-xylopyranoside ÏàËÆ¶È:88.8% Phytochemistry 1997 46 175-176 A stilbene xyloside from Holodiscus discolor bark Ruben F. Gonzalez-Laredo, Judith Chaidez-Gonzalez, Ahmed A. Ahmed, Joseph J. Karchesy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . Desoxyrhapontincin ÏàËÆ¶È:84.2% Archives of Pharmacal Research 2008 31 598-605 Lipoxygenase inhibitory constituents from rhubarb Tran Minh Ngoc, Pham Thi Hong Minh, Tran Manh Hung, Phuong Thien Thuong and IkSoo Lee, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . resveratrol 3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:83.3% Journal of Natural Products 1997 60 1082-1087 Isolation, Synthesis, and Antiplatelet Aggregation Activity of Resveratrol 3-O-¦Â-D-Glucopyranoside and Related Compounds Fulvia Orsini, Francesca Pelizzoni, Luisella Verotta, and Talal Aburjai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . (E)-resveratrol 3,5-O-¦Â-diglucoside C26H32O13 ÏàËÆ¶È:83.3% Planta Medica 2005 71 888-890 New Stilbenoid Glucosides Isolated from Vitis vinifera Cell Suspension Cultures (cv. Cabernet Sauvignon) Fabienne Larronde , Tristan Richard , Jean-Claude Delaunay ,Alain Decendit , Jean-Pierre Monti , St¨¦phanie Krisa, Jean-Michel M¨¦rillon Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 3-hydroxy-trans-stilbene-5-O-¦Â-D-glucoside ÏàËÆ¶È:83.3% Natural Product Research and Development 2005 17 434-436 Studies on the Chemical Constituents from Aerial Part of Dryopteris sublaeta ZHENG Xiao-ke; DONG San-li; FENG Wei-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . trans-resveratrol-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:80% Chinese Traditional and Herbal Drugs 2009 40 11-14 Chemical constituents from Smilax davidiana ZHANG Hong-sheng; KANG Li-ping; ZOU Peng; HAN Li-feng; XIONG Cheng-qi; ZHAO Yang; TAN Da-wei; MA Bai-ping; WEN De-jian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . piceid ÏàËÆ¶È:80% Natural Product Research and Development 2001 13(6) 16-18 STUDIES ON THE CHEMICAL CONSTITUENTS OF HYPOESTES TRIFLORA JIANG Bei; ZHAO Qin-shi; LIN Zhong-wen; LU Yang; ZHENG Qi-tai; SUN Han-dong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . (E)-piceatannol (3,5,3',4'-tetrahydroxystilbene) 3-O-¦Â-glucoside C20H22O9 ÏàËÆ¶È:78.9% Journal of Natural Products 1996 59 1189-1191 The Accumulation of Stilbene Glycosides in Vitis vinifera Cell Suspension Cultures Pierre Waffo Teguo, Alain Decendit, St¨¦phanie Krisa, G¨¦rard Deffieux, Joseph Vercauteren, and Jean-Michel M¨¦rillon Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . resveratrol-12-C-¦Â-glucopyranoside C20H22O8 ÏàËÆ¶È:77.7% Chemical & Pharmaceutical Bulletin 2000 48(7) 1001-1005 Stilbenoids Isolated from Stem Bark of Shorea hemsleyana Tetsuro ITO,Toshiyuki TANAKA, Yoshimi IDO,Ken-ichi NAKAYA, Munekazu IINUMA and Soedarsono RISWAN Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (Z)-resveratrol (3,5,4'-trihydroxystilbene) 3-O-¦Â-glucoside ÏàËÆ¶È:77.7% Journal of Natural Products 1996 59 1189-1191 The Accumulation of Stilbene Glycosides in Vitis vinifera Cell Suspension Cultures Pierre Waffo Teguo, Alain Decendit, St¨¦phanie Krisa, G¨¦rard Deffieux, Joseph Vercauteren, and Jean-Michel M¨¦rillon Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . (E)-Resveratrol 3-O-¦Á-D-glucopyranoside C20H23O8 ÏàËÆ¶È:77.7% Bulletin of the Korean Chemical Society 2009 30 703-706 A New Acylated Stilbene Glycoside from Acanthopanax brachypus Hao bin Hu, Jun Fan* Structure 13C NMR ̼Æ×Ä£Äâͼ |
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5Â¥2012-05-20 19:31:56













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