| ²é¿´: 277 | »Ø¸´: 2 | ||
Ñî´óËÉÖÁ×ðľ³æ (ÎÄ̳¾«Ó¢)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
|
|
̼Æ×Êý¾ÝÈçÏ£¬ÈܼÁÂȷ£º 18.9,72.5,80.2,81.8,104.8,109.9,111.1,112.0,130.7,143.5,143.7,151.8 ÐÁ¿à¸÷λÁË£¬Ð»Ð» |
» ²ÂÄãϲ»¶
293µ÷¼Á
ÒѾÓÐ7È˻ظ´
288Çóµ÷¼Á£¬Ò»Ö¾Ô¸»ªÄÏÀí¹¤´óѧ071005
ÒѾÓÐ5È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
307Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
283·ÖÇóµ÷¼Á
ÒѾÓÐ14È˻ظ´
Ò»Ö¾Ô¸211£¬0703»¯Ñ§305·ÖÇóµ÷¼Á
ÒѾÓÐ16È˻ظ´
»·¾³×¨Ë¶µ÷¼Á
ÒѾÓÐ13È˻ظ´
338Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Çó²ÄÁϵ÷¼Á£¬Ò»Ö¾Ô¸Ö£ÖÝ´óѧ289·Ö
ÒѾÓÐ17È˻ظ´
Ò»Ö¾Ô¸»ªÄÏʦ·¶´óѧ0702ÎïÀíѧ305µ÷¼Á
ÒѾÓÐ5È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´

jasminelw
Ìú¸Ëľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 269 (´óѧÉú)
- ½ð±Ò: 8813.7
- É¢½ð: 80
- ºì»¨: 6
- Ìû×Ó: 972
- ÔÚÏß: 604.2Сʱ
- ³æºÅ: 1858727
- ×¢²á: 2012-06-13
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ñî´óËÉ: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-04-23 10:36:43
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ñî´óËÉ: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-04-23 10:36:43
|
1 . (1Z)-atractylodin C13H10O ÏàËÆ¶È:92.3% Planta Medica 2001 67 437-442 Further Phenols and Polyacetylenes from the Rhizomes of Atractylodes lancea and their Anti-Inflammatory Activity M. Resch, J. Heilmann, A. Steigel, R. Bauer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . bis(5-((1E,7E)-nona-1,7-dien-3,5-diyn-1-yl)furan-2-yl)methane ÏàËÆ¶È:78.5% Fitoterapia 2012 83 199-203 A new 9-nor-atractylodin from Atractylodes lancea and the antibacterial activity of the atractylodin derivatives Yanjun Chen, Yuxue Wu, Hexiang Wang, Kun Gao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 9-Nor-atractylodin ÏàËÆ¶È:76.9% Fitoterapia 2012 83 199-203 A new 9-nor-atractylodin from Atractylodes lancea and the antibacterial activity of the atractylodin derivatives Yanjun Chen, Yuxue Wu, Hexiang Wang, Kun Gao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 1-(2-furyl)-(1E,7Z)-nonadiene-3,5-diyne-9-ol ÏàËÆ¶È:76.9% Fitoterapia 2012 83 199-203 A new 9-nor-atractylodin from Atractylodes lancea and the antibacterial activity of the atractylodin derivatives Yanjun Chen, Yuxue Wu, Hexiang Wang, Kun Gao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . trand-1,3,5,11-tridecatetraen-7,9-diyne C13H12 ÏàËÆ¶È:69.2% Phytochemistry 1997 45 695-699 Phototoxic polyacetylenes from Viguiera annua and adaptations of a chrysomelid beetle, Zygogramma continua, feeding on this plant Gabriel Guillet, Denise Chauret, John T. Arnason Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . acetylatractylodinol C15H12O3 ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2005 30 675-677 Studies on chemical constituents in roots of Peucedanum praeruptorum ZHANG Cun, XIAO Yongqing, TANIGUCH Massahiko, BABA Kimiye Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . angelidiol A C14H14O5 ÏàËÆ¶È:64.2% Chinese Chemical Letters 1993 4 885-886 TWO NEW COUMARINS FROM ANGELCIA PUBESCENS F.BISERRTA JIANG HUA LIU,YING JIE GUO,SUI XU XU,XIN SHENG YAO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . andangelidiol C14H14O5 ÏàËÆ¶È:64.2% Journal of Chinese Pharmaceutical Sciences 1997 6 122-422 Further Isolation of Coumarin from Angelica pubescence Maxim f.biserrata Shanet Yuan Jiang-Hua Liu, Sui-Xu Xu, Zhi-Yun Meng, Xin-Sheng Yao and Yu-Qiang Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . heramandiol C14H14O5 ÏàËÆ¶È:64.2% Acta Pharmaceutica Sinica 1996 31 63-67 FURTHER STUDIES ON CHEMICAL CONSTITUENTS OF ANGELICA PUBESCENS F BISERRATA JH Liu; SX Xu; XS Yao and YQ Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . bis(5-((1E,7E)-nona-1,7-dien-3,5-diyn-1-yl)furan-2-yl)isopropane ÏàËÆ¶È:62.5% Fitoterapia 2012 83 199-203 A new 9-nor-atractylodin from Atractylodes lancea and the antibacterial activity of the atractylodin derivatives Yanjun Chen, Yuxue Wu, Hexiang Wang, Kun Gao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 1,cis-3,trans-5,trans-11-tridecatetraen-7,9-diyne C13H12 ÏàËÆ¶È:61.5% Phytochemistry 1997 45 695-699 Phototoxic polyacetylenes from Viguiera annua and adaptations of a chrysomelid beetle, Zygogramma continua, feeding on this plant Gabriel Guillet, Denise Chauret, John T. Arnason Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 3,8,9,10-tetrahydroxy-6H-dibenzo[b,d]pyran-6-one C13H8O6 ÏàËÆ¶È:61.5% Journal of Agricultural and Food Chemistry 2008 56 393-400 Identification of Urinary and Intestinal Bacterial Metabolites of Ellagitannin Geraniin in Rats Hideyuki Ito, Ayumu Iguchi and Tsutomu Hatano Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 3-deoxy-3-iodo-1,2-O-isopropylidene-6-O-tosyl-¦Á-D-allofuranose ÏàËÆ¶È:61.5% Journal of Agricultural and Food Chemistry 2000 48 5283-5287 Synthesis and Antifungal Activity of Novel Bisdithiocarbamate Derivatives of Carbohydrates against Fusarium oxysporum f. sp. lini Catherine Rafin, Etienne Veignie, and Michel SancholleDenis Postel, Christophe Len, Pierre Villa, and Gino Ronco Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 5-(2,2-dimethyl-(4R)-1,3-dioxolan-4-yl)-6-(2-furyl)-2,2-diemthyl-(3aR,5R,6R,6aR)-perhydrofuro-[2,3-d][1,3]-dioxol-6-ol C15H18O7 ÏàËÆ¶È:60% Tetrahedron 2002 58 3801-3812 Synthesis of spiro carbon linked disaccharides from d-glucose, d- and l-arabinose G.V.M Sharma, V.Goverdhan Reddy, Palakodety Radha Krishna, A.Ravi Sankar, A.C Kunwar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 1-(1,3-Dihydro-4-hydroxy-1-isobenzofuranyl)butan-2,3-diol ÏàËÆ¶È:58.3% Journal of Natural Products 2002 65 876-882 Biologically Active Polyketide Metabolites from an Undetermined Fungicolous Hyphomycete Resembling Cladosporium Ulrich Höller,James B. Gloer, and Donald T. Wicklow Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 1-(1,3-Dihydro-4-hydroxy-1-isobenzofuranyl)butan-2,3-diol ÏàËÆ¶È:58.3% Journal of Natural Products 2002 65 876-882 Biologically Active Polyketide Metabolites from an Undetermined Fungicolous Hyphomycete Resembling Cladosporium Ulrich Höller,James B. Gloer, and Donald T. Wicklow Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . Esculetin C9H6O4 ÏàËÆ¶È:58.3% Acta Botanica Yunnanica 2007 29(2) 263-264 Chemical Constituents from Ceratophyllum demersum (Ceratophyllaceae) LU Xiao-Li,QIAO Ying, ZHANG Xian-Min, MA Bo-Lin, QIU Ming-Hua Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . Scopoletin C10H8O4 ÏàËÆ¶È:58.3% Chemistry of Natural Compounds 2009 45 896-897 CHEMICAL CONSTITUENTS FROM THE AERIALPARTS OF Sophora mollis Dong-Qing Fei, Mohammad Arfan,Jamal Rafiq, and Kun Gao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . scosoletin C10H8O4 ÏàËÆ¶È:58.3% Acta Botanica Sinica 2003 45 1003-1007 Two New Triterpenes from Neonauclea sessilifolia KANG Wen-Yi, LI Guo-Hong, HAO Xiao-Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 4H-1-benzopyran-4-one,5,7-dihydroxy-2-methyl C10H8O4 ÏàËÆ¶È:58.3% Acta Botanica Sinica 2003 45 1003-1007 Two New Triterpenes from Neonauclea sessilifolia KANG Wen-Yi, LI Guo-Hong, HAO Xiao-Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . esculetin C9H6O4 ÏàËÆ¶È:58.3% Journal of Chinese Pharmaceutical Sciences 1994 3 91-96 active constituents of Viola prionantha Bge. Bo Qin, Qing-Ping Chen and Zhi-Cen Lou Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-04-23 10:25:49
Ñî´óËÉ
ÖÁ×ðľ³æ (ÎÄ̳¾«Ó¢)
- Ó¦Öú: 243 (´óѧÉú)
- ½ð±Ò: 23878.3
- É¢½ð: 3
- ºì»¨: 46
- Ìû×Ó: 10466
- ÔÚÏß: 831.8Сʱ
- ³æºÅ: 1190374
- ×¢²á: 2011-01-15
- רҵ: »¯Ñ§ÉúÎïѧÓëÉúÎïÓлú»¯Ñ§

3Â¥2013-04-23 10:36:55














»Ø¸´´ËÂ¥