| ²é¿´: 273 | »Ø¸´: 1 | |||
zeng2010½ð³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
Çóһ΢Æ×Êý¾Ý лл
|
| 51.5,55.9,110.5,113.0,115.8,115.9,121.7,128.0,129.9,45.8,148.5,167.7 |
» ²ÂÄãϲ»¶
¸´ÊÔµ÷¼Á
ÒѾÓÐ11È˻ظ´
311Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
22408µ÷¼ÁÇóÖú
ÒѾÓÐ9È˻ظ´
085410 273Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁÏ¿¼Ñе÷¼Á
ÒѾÓÐ9È˻ظ´
085600²ÄÁÏÓ뻯¹¤329·ÖÇóµ÷¼Á
ÒѾÓÐ12È˻ظ´
0854µ÷¼Á
ÒѾÓÐ4È˻ظ´
µ÷¼ÁÇóÊÕÁô
ÒѾÓÐ14È˻ظ´
0831ÉúÒ½¹¤µÚÒ»ÂÖµ÷¼Áʧ°ÜÇóÖú
ÒѾÓÐ10È˻ظ´
Ò»Ö¾Ô¸¶«±±´óѧ¿ØÖƹ¤³Ì085406Êý¶þÓ¢¶þ385£¬Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
¸÷λ´óÏÀ°ï°ïæ~¹ØÓÚ΢ÉúÎïµÄ£¬Ð»Ð»£¡
ÒѾÓÐ10È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú£¬°ïæ·ÒëÒ»¶ÎÕªÒª£¨Î¢ÉúÎ£¬ººÒëÓ¢£¬·Ç³£¸Ðл£¬ÕæµÄ£¡
ÒѾÓÐ4È˻ظ´
ÎÒÓÃÏÔ΢¾µ×ö¸ïÀ¼ÊÏȾɫ¹Û²ì£¬¹ØÓÚÓ;µµÄÎÊÌ⡣ϣÍû´ó¼Ò¸øÎÒÖ¸Õý°ïæһÏÂллÁË
ÒѾÓÐ21È˻ظ´
ÇëÎÊ£¬Äܲ»ÄܰÑÁ½ÕÅDGGEͼÆ×Æ´ÔÚÒ»Æð·ÖÎö£¿Ð»Ð»£¡
ÒѾÓÐ13È˻ظ´
ÖØ½ðÇóÖú¹ØÓÚÀë×Ó½»»»Ê÷Ö¬²ãÎöÖù·ÖÀëÖÐÐÔ¶àÌǵIJÙ×÷£¬ÏÈÐÐлл¸÷λ
ÒѾÓÐ15È˻ظ´
ÇóÖú£¡Å©¸Ë¾úÇÖȾù¾úæß×ÓµÄÎÊÌ⡣лл´ó¼ÒÀ²
ÒѾÓÐ5È˻ظ´
ÇóÖúÒ»ÖÖ΢ÉúÎï¿ØÖÆ¼Á£¨É±¾ú¼Á£©µÄÖÐÎÄÃû³Æ£¬Ð»Ð»£¡
ÒѾÓÐ7È˻ظ´
°ïСŮ·Òëһϰɣ¡Ö÷ÒªÊÇÓе㿴²»Ã÷°×µ½µ×Ôõô×ö£¡Ð»Ð»£¨Î¢ÉúÎïÀࣩ
ÒѾÓÐ6È˻ظ´
΢ÄÉÃײÄÁÏÀà·½Ïò£¬Çë½Ì¸ßÊÖ·ÒëÒ»¶Î»°£¬ÂÛÎÄÖм±Ð裬лл£¡
ÒѾÓÐ1È˻ظ´
¡¾ÇóÖú¡¿ÔÚexcelÀï´¦ÀíÒ»ÏÂÊý¾ÝÇó΢·Ö£¬Çë¸ßÊÖÖ¸½ÌÒ»ÏÂ~ллÀ²~
ÒѾÓÐ15È˻ظ´
¡¾ÇóÖú/½»Á÷¡¿Çë½ÌÒ»¸ö¼òµ¥ÎÊÌ⣺ÐÂÂòµÄÔØ²£Æ¬ÐèÒªÇåϴô£¿¸Ç²£Æ¬ÄØ£¿Ð»Ð»£¡
ÒѾÓÐ18È˻ظ´
¶þÂȼ×Íé
½ð³æ (ÕýʽдÊÖ)
- Ó¦Öú: 105 (¸ßÖÐÉú)
- ½ð±Ò: 2190.7
- É¢½ð: 1870
- ºì»¨: 15
- Ìû×Ó: 538
- ÔÚÏß: 120.8Сʱ
- ³æºÅ: 1337209
- ×¢²á: 2011-07-04
- ÐÔ±ð: GG
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
leecius: ½ð±Ò+1, ллÌṩ£¡ 2012-07-04 09:11:13
zeng2010: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2012-07-04 17:03:59
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
leecius: ½ð±Ò+1, ллÌṩ£¡ 2012-07-04 09:11:13
zeng2010: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2012-07-04 17:03:59
|
1 . Methyl ferulate ÏàËÆ¶È:66.6% 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 2 . compound 6 C14H14N2O2 ÏàËÆ¶È:66.6% Heterocycles 2002 57 1501-1506 Synthesis of 1,4-Benzodiazepine-2,5-dione Derivatives Tong-Ing Ho,* Wen-Shiong Chen, Chi-Wei Hsu, Yeun-Min Tsai, and Jim-Min Fang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (Z)-¦Á-(2'-Bromo-4',5'-dimethoxyphenyl)-N-benzylnitrone C16H16BrNO3 ÏàËÆ¶È:61.5% Bioorganic & Medicinal Chemistry 2011 19 951-960 Synthesis, structure, theoretical and experimental in vitro antioxidant/pharmacological properties of ¦Á-aryl, N-alkyl nitrones,as potential agents for the treatment of cerebral ischemia Abdelouahid Samadi, Elena Soriano, Julia Revuelta, Carolina Valderas, Mourad Chioua,Ignacio Garrido, Bego?a Bartolom¨¦, Isabelle Tomassolli, Lhassane Ismaili, Laura Gonz¨¢lez-Lafuente,Mercedes Villarroya, Antonio G. Garc¨ªa, Mar¨ªa J. Oset-Gasque, Jos¨¦ Marco- Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound ÏàËÆ¶È:61.5% Canadian Journal of Chemistry 2007 85 66-76 Towards the development of a covalently tethered MALDI system - A study of allyl-modified MALDI matrixes Sanela Martic, John D. Brennan, Michael A. Brook, Suzanne Ackloo, and Noemi Nagy Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 2-((2-Carboxy-5-chlorophenyl)amino)-3-methoxybenzoic acid ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2011 19 2190-2198 Radiosynthesis and in vivo evaluation of 1-[18F]fluoroelacridar as a positron emission tomography tracer for P-glycoprotein and breast cancer resistance protein Bernd D?rner,Claudia Kuntner,Jens P. Bankstahl ,Thomas Wanek ,Marion Bankstahl ,Johann Stanek , Julia M¨¹llauer , Florian Bauer , Severin Mairinger,Wolfgang L?scher ,Donald W. Miller , Peter Chiba , Markus M¨¹ller, Thomas Erker , Oliver Langer Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . N-trans-p-hydroxyphenethylferolamine ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 2006 37 178-181 Chemical constituents from aerial parts of Argyreia seguinii CHANG Xiao-long; LI Jun; WU Li-jun; TU Pengfei Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . naamine F C20H24N3O3 ÏàËÆ¶È:58.3% Journal of Natural Products 2004 67 817-822 New Imidazole Alkaloids from the Indonesian Sponge Leucetta chagosensis Wafaa Hassan, RuAngelie Edrada, Rainer Ebel, Victor Wray, Albrecht Berg, Rob van Soest, Sumali Wiryowidagdo, and Peter Proksch Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . coniferyl alcohol ÏàËÆ¶È:58.3% Planta Medica 1982 46 145-148 Phenolic Glycosides of Paulownia tomentosa Bark O. Sticher and M. F. Lahioub Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ferulic acid ÏàËÆ¶È:58.3% Chemical & Pharmaceutical Bulletin 1983 31 156-161 Studies on the Constituents of the Stems of Tinospora tuberculata BEUMEE. I. N-trans- and N-cis-Feruloyl Tyramine, and a New Phenolic Glucoside, Tinotuberide NAOMICHI FUKUDA,MICHIKO YONEMITSU and TAKEATSU KIMURA Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 11 C13H16O6 ÏàËÆ¶È:58.3% Chemistry of Natural Compounds 1999 35 404-408 SYNTHESIS OF a-MONOGLYCERIDES OF AROMATIC ACIDS A. F. Artamonov, F. S. Nigmatullina,M. T. Aldabergenova, and B. Zh. Dzhiembaev Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Methyl caffeate ÏàËÆ¶È:58.3% Molecules 2000 5 153-161 Synthesis of 4-O-Methylcedrusin. Selective Protection of Catechols with Diphenyl Carbonate Stefaan M. O. Van Dyck, Guy L. F. Lemi¨¨re, Tim H. M. Jonckers and Roger Dommisse Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ferulicacid ÏàËÆ¶È:58.3% Journal of Chinese Pharmaceutical Sciences 2004 13 1-3 Chemical Constituents of Angelica sinensis LU Xin-hua; ZHANG Jin-juan; LIANG Hong; and ZHAO Yu-ying Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Ferulic acid ÏàËÆ¶È:58.3% Journal of Chinese Pharmaceutical Sciences 2006 15 251-254 Chemical Constituents from Roots of Semiaquilegia adoxoides NIU Feng, XIE Guang-bo, CUI Zheng, CHEN Fa-kui, and TU Peng-fei Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . trans-Caffeic acid methylate ÏàËÆ¶È:58.3% Journal of Chinese Pharmaceutical Sciences 2007 16 20-23 Chemical constituents of the unripe fruits of Evodia rutaecarpa Xiu-Wei Yang and Jie Teng Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ferulic acid C10H10O4 ÏàËÆ¶È:58.3% Acta Pharmaceutica Sinica 1995 30 526-530 STUDIES ON THE CHEMICAL CONSTITUENTS OF CONISELINUM V AGINATUM THELL RY Chen and DQ Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ferulic acid ÏàËÆ¶È:58.3% China Journal of Chinese Materia Medica 2007 32 409-413 Studies on chemical constituents of Salsola collina XIANG Yu, LI Youbin, ZHANG Jian, LI Ping, YAO Yuanzhang Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . ferulic acid ÏàËÆ¶È:58.3% China Journal of Chinese Materia Medica 2002 27 926-928 Studies on the Chemical Constituenst from Herba of Corallodiscus flabellata ZHENG Xiaoke, LI Jun, FENG Weisheng, BI Yuefeng, JI Chunru Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . isoferulic acid C10H10O4 ÏàËÆ¶È:58.3% Acta Pharmaceutica Sinica 2008 Vol 43 1208-1210 A novel compound isolated from the peels of Citrus changshan-huyou Y.B.Chang ZHAO Xue-mei; YE Xing-qian; ZHU Da-yuan Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . ferulic acid ÏàËÆ¶È:58.3% Acta Pharmaceutica Sinica 2004 Vol 39 41-45 Isolation and structural identification of chemical constituents from Selaginella tamariscina (Beauv.)Spring BI Yue feng; ZHENG Xiao ke; FENG Wei sheng; SHI She po Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 1-methyl caffeic acid ÏàËÆ¶È:58.3% Natural Product Sciences 2005 11 75-78 A New Acetophenone of Aerial Parts from Rumex aquatica Yoon, Hwan-Min; Park, Ji-Yeun; Oh, Mi-Hyun; Kim, Kyung-Hee; Han, Jung-Hoon; Whang, Wan-Kyunn Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . curculactone A C12H14O4 ÏàËÆ¶È:58.3% Bioorganic & Medicinal Chemistry Letters 2011 21 1512-1514 Enhancement of pancreatic lipase inhibitory activity of curcumin by radiolytic transformation Tae Hoon Kim, Jae Kyung Kim, Hideyuki Ito , Cheorun Jo Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . Methyl 4-hydroxy-3-methoxybenzoate ÏàËÆ¶È:58.3% Canadian Journal of Chemistry 2007 85 66-76 Towards the development of a covalently tethered MALDI system - A study of allyl-modified MALDI matrixes Sanela Martic, John D. Brennan, Michael A. Brook, Suzanne Ackloo, and Noemi Nagy Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . Coniferyl alcohol ÏàËÆ¶È:58.3% Planta Medica 1982 46 145-148 Phenolic Glycosides of Paulownia tomentosa Bark 0. Sticher and M. F. Lahioub Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 5,6-Dibromo-L-hypaphorine C14H17N2O2Br2 ÏàËÆ¶È:58.3% Marine drugs 2011 9 879-888 Bioactive Indole Derivatives from the South Pacific Marine Sponges Rhopaloeides odorabile and Hyrtios sp. Arlette Longeon,Brent R. Copp,Elodie Qu¨¦vrain,M¨¦lanie Rou¨¦,Betty Kientz,Thierry Cresteil,Sylvain Petek,C¨¦cile Debitus and Marie-Lise Bourguet-Kondracki Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 3-(3',4'-dimethoxyphenyl)-(R)-lactic acid methyl ester ÏàËÆ¶È:58.3% Phytochemistry 1990 29 2645-2649 Two caffeic acid tetramers having enantiomeric phenyldihydronaphthalene moieties from Macrotomia euchroma Makoto Nishizawa,Masashi Tsuda,Koji Hayashi Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 2-[(3,4-dimethoxyphenyl)methyl]-2-methyl-1,3-dioxolane C13H18O4 ÏàËÆ¶È:58.3% Journal of Heterocyclic Chemistry 2006 43 1539-1547 Synthesis of 8,9-dialkoxybenzodiazepines and 7,8-dialkoxyisoquinolines L¨¦szl¨® Pong¨®,J¨®zef Reiter,Gyula Simig,B¨¦la ¨¢gai and Ferenc Faigl Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . compound 7c C14H14O5 ÏàËÆ¶È:58.3% Journal of Heterocyclic Chemistry 2000 37 751-755 The birch reduction of heterocyclic compounds V Birch reduction of 2- and 5-acylfuran-3-carboxylic acids and reductive elimination of 2-(arylmethoxymethyl)furan-3-carboxylic acids Yasuo Ohta, Matsumi Doe, Yoshiki Morimoto and Takamasa Kinoshita Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . methylcaffeate ÏàËÆ¶È:58.3% China Journal of Chinese Materia Medica 2010 35 1142-1144 Flavonoids and phenolic acid derivatives from Flos Farfarae WU Di; ZHANG Mian; ZHANG Chaofeng; WANG Zhengtao Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . ferulic acid ÏàËÆ¶È:58.3% Chinese Traditional and Herbal Drugs 2009 40 844-846 Chemical constituents from root of Polygala fallax ZHONG Ji-qiang; DI Bin; FENG Feng Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . Ëɰش¼ C10H12O3 ÏàËÆ¶È:58.3% Chinese Traditional and Herbal Drugs 2009 40 1873-1876 ÌúƤʯõú»¯Ñ§³É·ÖµÄÑо¿ ¹Ü»Ý¾ê;ÕÅÑ©;ÍÀ·ï¾ê;Ò¦ÐÂÉú Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . caffeic acid methyl ester ÏàËÆ¶È:58.3% Chinese Traditional and Herbal Drugs 2007 38 342-344 Chemical constituents in Ficus tikoua of Miao nationality GUAN Yong-xia; YANG Xiao-sheng; TONG Li-hua; YANG Bo; HAO Xiao-jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . 3-ôÇ»ù-4-¼×Ñõ»ùÈâ¹ðËá ÏàËÆ¶È:58.3% Chinese Traditional and Herbal Drugs 2002 33 405-406 ¹óÖݷ佺ÖеÄÓлúËá³É·ÖÑо¿ ºØá¿áÉ,ÅËÎÀ¶«,¬ÓñÕñ,Õų¤¸ý,Ô¬ÄÁ Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . ferulic acid ÏàËÆ¶È:58.3% Chinese Traditional and Herbal Drugs 1997 28 259-262 Studies on the Chemical Constituents of Glandularstalk St. Paulswort (Siegesbeckia pubescens)(¢ñ) Fu Hongzheng; Lou Zhicen; Yang Xiuwei; et al(National Laboratory of Natural arid Biomimetic Drugs; Beijing Medical University; Beijing); Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . trans-ferulic acid ÏàËÆ¶È:58.3% Archives of Pharmacal Research 1992 15 322-327 Phytochemical study on Catalpa ovata Han Suk Young, Min Sun Kim, Hee Juhn Park, Hae Young Chung and Jae Sue Choi Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . Methyl caffeate ÏàËÆ¶È:58.3% Archives of Pharmacal Research 2002 25 325-328 Anti-platelet effect of the constituents isolated from the barks and fruits of Magnolia obovata Mi Kyung Pyo, YongYook Lee and Hye Sook Yun-Choi Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . Ferulic acid ÏàËÆ¶È:58.3% Archives of Pharmacal Research 2010 33 515-521 A new phenylpropane glycoside from the rhizome of Sparganium stoloniferum Seung Young Lee, Sang Un Choi, Jei Hyun Lee, Dong Ung Lee and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2012-07-04 08:11:25













»Ø¸´´ËÂ¥
100