| ²é¿´: 384 | »Ø¸´: 1 | |||
lizhaoyun½ð³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×15¸ö½ð±Ò£¬
|
|
1 13C NMR (100 MHz, MeOD) ¦Ä 31.70,45.73,62.54,71.17,74.87,78.17,78.29,102.55,104.07,111.02,121.66,126.93,129.43,129.53,133.43, 142.97,160.31,164.39,202.61. 2 13C NMR (101 MHz, MeOD) ¦Ä38.77,39.20,62.47,71.34,74.87,77.99,78.06,102.20,102.65,109.14,110.66,126.86,129.28,129.54, 145.39,159.27,160.12. |
» ²ÂÄãϲ»¶
²ÄÁϹ¤³Ì085601£¬270Çóµ÷¼Á
ÒѾÓÐ24È˻ظ´
085404 293Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
µ÷¼Á
ÒѾÓÐ21È˻ظ´
¸´ÊÔµ÷¼Á£¬Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤289·Ö
ÒѾÓÐ15È˻ظ´
08¹¤¿ÆÇóµ÷¼Á290·Ö
ÒѾÓÐ12È˻ظ´
286Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
²ÄÁÏÀà284µ÷¼Á
ÒѾÓÐ24È˻ظ´
¿¼Ñе÷¼Á-²ÄÁÏÀà-284
ÒѾÓÐ14È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
Ò»Ö¾Ô¸985³õÊÔ354·ÖÉúÎïµ÷¼Á
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
½¨ÒéȺÖ÷¿ªÒ»¸ö΢Æ×ÇóÖúרÀ¸°É
ÒѾÓÐ14È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
10½ð±ÒÇóÖú΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
ÇóÖú3¸öÓÃ΢Æ×½âÎöµÄ½á¹¹
ÒѾÓÐ8È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú½âÆ× ¸öÈ˾õµÃÊÇ»ÆÍª
ÒѾÓÐ16È˻ظ´
ÇóÖú£¬É¢¾¡½ð±Ò¡ª¡ª½âÆ×
ÒѾÓÐ3È˻ظ´
¡¾ÇóÖú¡¿¼Û´øÆ× 5½ð±Ò
ÒѾÓÐ6È˻ظ´

wm0629
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 341 (´óѧÉú)
- ½ð±Ò: 6381.8
- ºì»¨: 3
- Ìû×Ó: 1962
- ÔÚÏß: 77.9Сʱ
- ³æºÅ: 2217415
- ×¢²á: 2013-01-01
- ÐÔ±ð: GG
- רҵ: ÖÐÒ©ÅÚÖÆ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
lizhaoyun: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2013-04-21 18:27:56
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
lizhaoyun: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2013-04-21 18:27:56
|
»¯ºÏÎï1£º 1 . cynanoneside B ÏàËÆ¶È:68.4% Archives of Pharmacal Research 2011 34 2021-2027 Chemical constituents of Cynanchum wilfordii and the chemotaxonomy of two species of the family Asclepiadacease, C. wilfordii and C. auriculatum YanFu Jiang, Hyun Gyu Choi, Ying Li, Yu Mi Park and Jong Hwa Lee, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . gnetifolin E ÏàËÆ¶È:63.1% Helvetica Chimica Acta 2008 Vol. 91 159 Stilbene Derivatives from Gnetum montanum Markgr. f. megalocarpum Markgr. Li-Qin Wang, You-Xing Zhao, Jiang Miao Hu, Ai-Qun Jia, and Jun Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (3R)-O-¦Â-D-glucopyranosyloxy-5-phenylvaleric acid C17H24O8 ÏàËÆ¶È:63.1% Journal of Natural Products 1999 62 1101-1105 Phenylvaleric Acid and Flavonoid Glycosides from Polygonum salicifolium Ihsan Calis, Ayse Kuru¨¹ z¨¹m, L. Öm¨¹ r Demirezer, Otto Sticher, Walter Ganci, and Peter R¨¹ edi Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 2,4-Dihydroxy-3,5-dimethyl-6-O-glucosyl-benzophenone C21H24O9 ÏàËÆ¶È:63.1% Chemistry of Natural Compounds 2011 Vol. 47, No. 4 632-635 PHENOLIC COMPOUNDS FROM THE LEAVES OF Psidium guajava.I. HYDROLYSABLE TANNINS AND BENZOPHENONE GLYCOSIDES Byoung-Jae Park, Tomohiko Matsuta, Tsutomu Kanazawa,Kwang-Jin Chang, Cheol-Ho Park, and Michio Onjo Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-phenyl-1-(2',6'-dihydroxy-phenyl-4'-O-¦Â-D-glucopyranosyl)-1-propanone ÏàËÆ¶È:63.1% Acta Botanica Yunnanica 2010 32 455-462 A New Lignan from Elaeagnus lanceolata (Elaeagnaceae) SONG We i-Wu, LIBo, LIU Ji-Kai Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . plataplatanoside C20H22O10 ÏàËÆ¶È:60% Journal of Natural Products 2000 63 1417-1419 Phenolic Glycosides from the Leaves of Alangium platanifolium var.platanifolium Akie Tamaki, Toshinori Ide, and Hideaki Otsuka Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 2,3'-dihydroxy-4-methoxy-benzophenone-6-O-¦Â-glucopyranoside C20H22O10 ÏàËÆ¶È:60% Phytochemistry Letters 2011 4 459-461 New benzophenone glucosides from the aerial parts of Gentiana verna L. subsp. pontica (Soltok.) Hayek Duygu Kaya, Funda Nuray Yalçın, Erdal Bedir, İhsan Çalış, Lisa Steinhauser, Klaus Albert, Tayfun Ersöz Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . juglanoside A C16H20O7 ÏàËÆ¶È:57.8% Chemical & Pharmaceutical Bulletin 2004 52(5) 566-569 New ¦Á-Tetralonyl Glucosides from the Fruit of Juglans mandshurica Lijuan LIU,Wei LI,Kazuo KOIKE, Shujie ZHANG,and Tamotsu NIKAIDO Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . cis-resveratrol-3,4'-O-¦Â-diglucoside C20H32O13 ÏàËÆ¶È:57.8% Phytochemistry 2002 60 795-798 Galloylated catechins and stilbene diglucosides in Vitis vinifera cell suspension cultures Alain Decendit, Pierre Waffo-Teguo, Tristan Richard, St¨¦phanie Krisa, Joseph Vercauteren, Jean-Pierre Monti, G¨¦rard Deffieux, Jean-Michel M¨¦rillon Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . benzyl 2-O-¦Â-D-glucopyranosyl-2,6-dihydroxybenzoate C20H22O9 ÏàËÆ¶È:57.8% Phytochemistry 2001 58 1073-1081 Potential allelochemicals from Sambucus nigra Brigida D¡¯Abrosca, Marina DellaGreca, Antonio Fiorentino, Pietro Monaco,Lucio Previtera, Ana M. Simonet, Armando Zarrelli Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (Z)-resveratrol (3,5,4'-trihydroxystilbene) 3-O-¦Â-glucoside ÏàËÆ¶È:57.8% 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 12 . isocochinolide-7¦Á-¦Â-glucopyranoside C21H24O9 ÏàËÆ¶È:57.8% Natural Product Research 2007 21 1191-1198 Three new 3-benzylbenzofuran-2-one derivatives from Homalium brachybotrys (Flacourtiaceae/Salicaceae s. l.) Ashik Mosaddik; Paul I. Forster; Peter G. Waterman Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 3-(4 ¦Â-D-glucopyranosyloxy-3-methoxy)-phenyl-2E-propenol ÏàËÆ¶È:57.8% Phytochemistry 1998 49 1299-1304 Antialgal compounds from zantedeschia aethiopica Marina Della Grec¦Á, Maria Ferrar¦Á, Antonio Fiorentino, Pietro Monaco, Lucio Previtera Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . nepetanudoside D C16H22O8 ÏàËÆ¶È:57.8% Phytochemistry 1996 42 1085-1088 Nepetanudosides and iridoid glucosides having novel stereochemistry from Nepeta nuda ssp. Albiflora Yoshio Takeda, Tetsuo Yagi, Takashi Matsumoto, Gisho Honda, Mamoru Tabata, Tetsuro Fujita, Tetsuro Shingu, Hideaki Otsuka, Ekrem Sezik, Erdem Yesilada Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . piceid C20H22O8 ÏàËÆ¶È:57.8% 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 16 . 3,5-dihydroxy-stilbene-3-O-¦Â-D-glucoside ÏàËÆ¶È:57.8% 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 17 . polydotin peceid ÏàËÆ¶È:57.8% 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 18 . Z-piceatannol 3'-O-¦Â-glucopyranoside ÏàËÆ¶È:57.8% Phytochemistry 1989 28 2071-2078 Structures and accumulation patterns of soluble and insoluble phenolics from norway spruce needles Dieter Strack,J¨¹rgen Heilemann,Victor Wray,Herbert Dirks Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . ÐÂÒì¸Ê²ÝÜÕ C21H22O9 ÏàËÆ¶È:57.8% Chinese Traditional and Herbal Drugs 2008 39 825-828 µá»Æ¾«µÄ»¯Ñ§³É·ÖÑо¿(¢ò) ÀîÏþ;À´¹ú·À;ÍõÒ×·Ò;Õű£¹ú;ÂÞÊ¿µÂ Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . liquiritin ÏàËÆ¶È:57.8% Archives of Pharmacal Research 2005 28 1239-1243 Norditerpenoid alkaloids and other components from the processed tubers of aconitum carmichaeli Sang Hee Shim, So Young Lee, Ju Sun Kim, Kun Ho Son and Sam Sik Kang Structure 13C NMR ̼Æ×Ä£Äâͼ »¯ºÏÎï2£º 1 . 3,5,4'-trihydroxy-bibenzyl-3-O-¦Â-D-glucoside ÏàËÆ¶È:83.3% 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 2 . grevilloside A C17H24O8 ÏàËÆ¶È:76.4% Phytochemistry 2008 69 2749-2752 Grevillosides A¨CF: Glucosides of 5-alkylresorcinol derivatives from leaves of Grevillea robusta Yukiko Yamashita, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . batatsin III-3-O-glucoside C21H26O8 ÏàËÆ¶È:71.4% Phytochemistry 1997 44 1565-1567 Two bibenzyl glucosides from Pleione bulbocodioides Li Bai, Noriko Masukawa, Masae Yamaki, Shuzo Takagi Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . grevilloside B C17H26O8 ÏàËÆ¶È:70.5% Phytochemistry 2008 69 2749-2752 Grevillosides A¨CF: Glucosides of 5-alkylresorcinol derivatives from leaves of Grevillea robusta Yukiko Yamashita, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . grevilloside C C17H24O9 ÏàËÆ¶È:70.5% Phytochemistry 2008 69 2749-2752 Grevillosides A¨CF: Glucosides of 5-alkylresorcinol derivatives from leaves of Grevillea robusta Yukiko Yamashita, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . grevilloside D C16H24O8 ÏàËÆ¶È:70.5% Phytochemistry 2008 69 2749-2752 Grevillosides A¨CF: Glucosides of 5-alkylresorcinol derivatives from leaves of Grevillea robusta Yukiko Yamashita, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . grevilloside E C16H22O9 ÏàËÆ¶È:70.5% Phytochemistry 2008 69 2749-2752 Grevillosides A¨CF: Glucosides of 5-alkylresorcinol derivatives from leaves of Grevillea robusta Yukiko Yamashita, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Á,¦Â-dihydrorhaponticin C21H26O9 ÏàËÆ¶È:66.6% Phytochemistry 2006 67 2182-2188 Stilbenoids from Tragopogon orientalis Christian Zidorn, Sandra Grass, Ernst P. Ellmerer,Karl-Hans Ongania, Hermann Stuppner Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (Z)-resveratrol (3,5,4'-trihydroxystilbene) 3-O-¦Â-glucoside ÏàËÆ¶È:66.6% 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 10 . piceid C20H22O8 ÏàËÆ¶È:66.6% 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 11 . 3,5-dihydroxy-stilbene-3-O-¦Â-D-glucoside ÏàËÆ¶È:66.6% 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 12 . polydotin peceid ÏàËÆ¶È:66.6% 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 13 . Piceid ÏàËÆ¶È:66.6% 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 14 . 3-hydroxy-trans-stilbene-5-O-¦Â-D-glucoside ÏàËÆ¶È:66.6% 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 . compound 18 C20H8O22 ÏàËÆ¶È:66.6% Food Chemistry 2012 135 2086-2094 Chemical and antifungal investigations of six Lippia species (Verbenaceae)from Brazil Cristiano Soleo Funari , Fernanda Patr¨ªcia Gullo , Assunta Napolitano , Renato Lajarim Carneiro ,Maria Jos¨¦ Soares Mendes-Giannini , Ana Marisa Fusco-Almeida , Sonia Piacente , Cosimo Pizza ,Dulce Helena Siqueira Silva Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . trans-resveratrol glucoside ÏàËÆ¶È:66.6% Journal of Agricultural and Food Chemistry 2004 52 5396-5403 Determination of Piceid and Resveratrol in Spanish Wines Deriving from Monastrell (Vitis vinifera L.) Grape Variety Juan F. Moreno-Labanda, Ricardo Mallavia, Laura P¨¦rez-Fons, Victoria Lizama, Domingo Saura, and Vicente Micol Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Resveratrol-3-O-¦Â-D-glucoside C20H22O8 ÏàËÆ¶È:66.6% Natural Product Research and Development 2012 24 757-760 Chemical Constituents from Stems of Rhododendron delavayi Franch. XU Jin-jin; WANG Yue-hu; WANG Hong-sheng; WANG Huan; HUANG Qiao-qin; LONG Chun-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 1-(3',5'-dihydroxy)phenyl-2-(4''-O-¦Â-D-glucopyranosyl) phenylethane C20H24O8 ÏàËÆ¶È:65% Fitoterapia 2011 82 481-484 New bibenzyl glycosides from leaves of Camellia oleifera Abel. with cytotoxic activities Yuelong Chen, Ling Tang, Baomin Feng, Liying Shi, Huiguo Wang, Yongqi Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . grevilloside F C15H18O9 ÏàËÆ¶È:64.7% Phytochemistry 2008 69 2749-2752 Grevillosides A¨CF: Glucosides of 5-alkylresorcinol derivatives from leaves of Grevillea robusta Yukiko Yamashita, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . orcinol glucoside C13H18O7 ÏàËÆ¶È:64.7% Acta Botanica Yunnanica 2003 25(6) 711-715 A New Lignan Glycoside from Curculigo capitulata LI Ning,TAN Ning-Hua,ZHOU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . Grevilloside G C14H20O8 ÏàËÆ¶È:64.7% Journal of Natural Medicines 2010 64 474-477 5-Alkylresorcinol glucosides from the leaves of Grevillea robusta Allan Cunningham Yukiko Yamashita, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato and Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-04-21 17:46:03













»Ø¸´´ËÂ¥