| ²é¿´: 776 | »Ø¸´: 3 | ||
ÐþìÇ½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×Êý¾ÝÇóÖú....!
|
|
MeOD 169.20,156.92,149.84,149.31,142.02,131.34,131.21,130.73,130.68,128.32,123.22,118.79,116.49,116.28,111.61,56.42,42.53,35.80. ÏÈлÁË~ |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸ÄϾ©º½¿Õº½Ìì´óѧ ²ÄÁÏÓ뻯¹¤329·ÖÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Ò»Ö¾Ô¸C9µÄ»¯Ñ§¹¤³Ì£¨085602£© 340·Ö£¬¸Ð¾õУÄÚµ÷¼ÁÎÞÍû£¬Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
312Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
²ÄÁÏר˶322
ÒѾÓÐ9È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
085600²ÄÁÏÓ뻯¹¤301·ÖÇóµ÷¼ÁԺУ
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸ ½ÄÏ´óѧ 085602 »¯¹¤×¨Ë¶ 338·ÖÇóµ÷¼Á
ÒѾÓÐ14È˻ظ´
070300»¯Ñ§Ñ§Ë¶311·ÖÇóµ÷¼Á
ÒѾÓÐ13È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ9È˻ظ´
Ò»Ö¾Ô¸ºÓ±±¹¤Òµ´óѧ²ÄÁϹ¤³Ì£¬³õÊÔ344Çóר˶µ÷¼Á
ÒѾÓÐ4È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÕæµÄͦ²»´íµÄ£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý12
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾ÝÇóÖú¡ª¡ªÈý¸ö»¯ºÏÎï лл£¡
ÒѾÓÐ8È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
Çó΢Æ×Êý¾Ý лл
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
Çó´óϺ²é΢Æ×£¬Íò·Ö¸Ðл°¡£¡£¡£¡
ÒѾÓÐ3È˻ظ´
΢Æ×²é½á¹¹£¬ÓÐÆ×ͼ
ÒѾÓÐ3È˻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´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
2Â¥2013-11-16 15:18:55
ÐþìÇ
½ð³æ (СÓÐÃûÆø)
- Ó¦Öú: 3 (Ó×¶ùÔ°)
- ½ð±Ò: 1201.2
- É¢½ð: 32
- Ìû×Ó: 214
- ÔÚÏß: 167.2Сʱ
- ³æºÅ: 1069436
- ×¢²á: 2010-08-04
- רҵ: ÌìȻҩÎﻯѧ
3Â¥2013-11-16 15:32:15
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï
ÐþìÇ: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-02-25 22:20:08
ÐþìÇ: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-02-25 22:20:08
|
²éѯ½á¹û£º¹²²éµ½875¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . feruloyltyramine C18H19NO4 ÏàËÆ¶È:94.4% Chemistry of Natural Compounds 1996 32 932-1028 ALKALOIDS. PLANTS, STRUCTURES, PROPERTIES" Chapter , continued R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova,S. F. Aripova, I. A. Israilov, M. N. Sultankhodzhaev,V. I. Vinogradova, V. I. Akhmedzhanova, T. S. Tulyaganov,B. T. Salimov, and V. A. Tel'nov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . compound 1b ÏàËÆ¶È:94.4% Phytochemistry 1982 21 2979-2980 Feruloyltyramine from Hypecoum S. Fazal Hussain, Belkis Gözler, Maurice Shamma, Tekant Gözler Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . N-trans-feruloyltyramine ÏàËÆ¶È:94.4% Natural Product Research and Development 2006 18 958-961 Isolation and Structral Identification of Chemical Constituents from Anabasis brevifolia CHEN Hua; HajiA¡¤Aisa; LI Yuan-chao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . N-(E)-feruloyltyramine C18H19NO4 ÏàËÆ¶È:94.4% Natural Product Communications 2012 7 1047-1020 Amides and an Alkaloid from Portulaca oleracea Tetsuo Kokubun, Geoffrey C. Kite, Nigel C. Veitch and Monique S. J. Simmonds Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . N-trans-feruloiltiramina C18H19NO4 ÏàËÆ¶È:94.4% Qu¨ªmica Nova 2013 36 1111-1115 CONSTITUINTES QUÍMICOS DE Solanum buddleifolium Sendtn Francisco das Chagas L. Pinto, Maria da Conceição M. Torres, Edilberto R. Silveira e Ot¨ªlia Deusd¨ºnia L. Pessoa*,Raimundo Braz-Filho,Maria Lenise da Silva Guedes Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . p-hydroxyphenethyl trans-ferulate C18H18O5 ÏàËÆ¶È:88.8% Phytochemistry 2003 1179-1184 Ecdysteroids and other constituents from Sida spinosa L. Faten M.M. Darwish, Manfred G. Reinecke Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . N-trans-feruloyltyramine C18H19O4N ÏàËÆ¶È:88.8% Acta Pharmaceutica Sinica 2009 Vol 44 764−767 New homoisoflavanones from Polygonatum odoratum(Mill.) Druce LI Li-hong; REN Feng-zhi; CHEN Shu-hong; GAO Yue-qi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . E-N-feruloyltyramine ÏàËÆ¶È:88.8% Korean Journal of Pharmacognosy 1997 28(3) 112-116 Studies on the Constituents of Hibiscus syriacus (I) Lee, In-Kyoung; Ryoo, In-Ja; Choung, Dong-Ho; Han, Kyou-Hoon; Yun, Bong-Sik; Yoo, Ick-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . N-trans-feruloyl tyramine C18H19NO4 ÏàËÆ¶È:88.8% Natural Product Research 2011 Vol. 25, No. 13 1243-1249 Chemical constituents from the roots of Xanthium sibiricum Suqin Kan, Guangying Chen, Changri Han, Zhong Chen, Xinming Song, Ming Ren and Hong Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . N-trans-Feruloyltyramine C18H19NO4 ÏàËÆ¶È:88.8% Journal of Natural Medicines 2009 63 331-334 A new amide from the leaves and twigs of Litsea auriculata Hitoshi Tanaka, Saya Yatsuhashi, Tadashi Yasuda, Masaru Sato and Eiji Sakai, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (2,3)-trans N-(p-hydroxyphenethyl)ferulamide C18H11O4N ÏàËÆ¶È:88.8% Chinese Traditional and Herbal Drugs 2003 34 101-104 Studies on chemical constituents of Diploclisia glaucescens HUANG Xiao chun; GUO Yue wei; WANG Zheng tao; ZHOU Wen liang; ZUO Jian ping Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . N-trans-feruloyl tyramine ÏàËÆ¶È:88.8% Chinese Traditional and Herbal Drugs 2010 41 1950-1952 Èý°×²ÝµÄ»¯Ñ§³É·ÖÑо¿ Åí±ù;ºÎ´ºÄê;ÐíÀû¼Î;Фΰ;ÅíÓÂ;ФÅà¸ù Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 7'-(3',4'-dihydroxyphenyl)-N-{(4-methoxyphenyl)ethyl}propenamide C18H19NO4 ÏàËÆ¶È:88.8% Chinese Journal of Natural Medicines 2005 3 151-154 Studies on the Active Constituents of Fissistigma oldhamii ZHENG Zong-Ping; LIANG Jing-Yu; HU Li-Hong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . N-trans-feruloyltyramine ÏàËÆ¶È:88.8% Archives of Pharmacal Research 2005 28 1224-1227 Cytotoxic constituents from the whole plant of corydalis pallida Hyang Rim Kim, Hye -Young Min, Yeon Hee Jeong, Sang Kook Lee and Nam Sook Lee, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . N-trans-feruloyltyramine C18H19O4N ÏàËÆ¶È:88.8% Chinese Pharmaceutical Journal 2006 41 94-96 Studies on Chemical Constituents in Stems of Porana sinensis Hemsl. ZHANG Chao-feng, ZHANG Zi-jia, ZHANG Mian, WANG Zheng-tao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . moupinamide ÏàËÆ¶È:88.8% Chinese Pharmaceutical Journal 2010 45 975-979 Phenolic Components and Flavanones from Dendrobium candidum LI Yan, WANG Chun-lan, WANG Fang-fei, DONG Hai-ling, GUO Shun-xing, YANG Jun-shan, XIAO Pei-gen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 7'-(4'-hydrox yphenyl) ethyl]-E-8-propenamide ÏàËÆ¶È:88.8% Chinese Journal of Medicinal Chemistry 2004 14 326-331 Phenolic compounds from Sargentodoxa cuneata(Oliv.) Rehd. et Wils. and their antitumor activities MAO Shui-chun, GU Qian-qun, CUI Cheng-bin, HAN Bing, CAI Bing, LIU Hong-bing Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . N-trans-feruloyl tyramine ÏàËÆ¶È:88.8% Journal of Shenyang Pharmaceutical University 2007 24 79-81 Chemical constituents of Sinomenium acutum SONG Yong-bin, CHENG Wei-ming, QU Ge-xia, QIU Feng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . cis-N-(p-hydroxyphenethyl)ferulamide ÏàËÆ¶È:88.8% Natural Product Research and Development 2008 20 816-820 Chemical Constituents of Oxyria digyna LI Xing-yu;LONG Chun-lin;WANG Yue-hu; GUO Rong; Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . trans-N-feruloyltyramine ÏàËÆ¶È:88.8% Molecules 2012 17 2675-2682 Bioactive Phenolic Amides from Celtis africana Areej Mohammad Al-Taweel, Shagufta Perveen, Azza Muhammed El-Shafae, Ghada Ahmed Fawzy, Abdul Malik, Nighat Afza, Lubna Iqbal and Mehreen Latif Structure 13C NMR ̼Æ×Ä£Äâͼ |
4Â¥2013-11-16 17:03:03














»Ø¸´´ËÂ¥