| ²é¿´: 316 | »Ø¸´: 1 | ||
xzhfoodÈÙÓþ°æÖ÷ (ÖøÃûдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý1¸ö ÒÑÓÐ1È˲ÎÓë
|
|
JHF-22 ÈܼÁ£ºDMSO ̼Æ×Êý¾Ý£º 27.1,54.7,109.6,111.2,118.2,118.3,120.8,123.9,126.3,127.2,128.2,129.3,136.3,170.1 |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ4È˻ظ´
±¾9Ò»Ö¾Ô¸2 0854µÍ·Öר˶286Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
298Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
²ÄÁÏרҵ344Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
282£¬µçÆø¹¤³Ìרҵ£¬Çóµ÷¼Á£¬²»Ìôרҵ
ÒѾÓÐ6È˻ظ´
301Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ28È˻ظ´
²ÄÁÏ085601µ÷¼Á
ÒѾÓÐ17È˻ظ´
Ò»Ö¾Ô¸0703»¯Ñ§ÕÐ61×îÖÕÅÅÃû62»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ23È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾ÝÒ»¸ö
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Íò·Ö¸Ðл£¡£¡£¡£¨GJ-R-30-35-2-4-3£©
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý1¸ö
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾ÝÒ»¸ö!
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúÒ»¸ö΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²é»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
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
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
xzhfood: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-30 13:37:38
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
xzhfood: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-30 13:37:38
|
²éѯ½á¹û£º¹²²éµ½135¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . L-Tryptophan C11H12N2O2 ÏàËÆ¶È:78.5% Journal of Chinese Pharmaceutical Sciences 2004 13 81-86 Chemical Constituents from Starfish Asterias rollestoni LI Guoqiang, DENG Zhi-wei, LI Jun, FU Hon-zheng, and LIN wen-han Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . tryptophan C11H12N2O2 ÏàËÆ¶È:78.5% Natural Product Research 2006 20 79-83 A new adenosyl-alkaloid from Ostrea rivularis Ming-An Ouyang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . tryptophan ÏàËÆ¶È:78.5% Natural Product Sciences 2001 7 107-109 Anti-diabetic Constituent from the Node of Lotus Rhizome (Nelumbo nucifera Gaertn) Lee, Min-Won; Kim, Jun-Sik; Cho, Su-Min; Kim, Ji-Hun; Lee, Jae-Seung Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . tryptophan ÏàËÆ¶È:78.5% Korean Journal of Pharmacognosy 2011 42 302-308 Inhibitors of Adipogenesis in 3T3-L1 Cells Isolated from Wheat Bran Jeong, Won-Sik; Hong, Seong-Su; Lee, Jung-A; Ahn, Eun-Kyung; Oh, Joa-Sub Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . banegasine ÏàËÆ¶È:78.5% Chinese Traditional and Herbal Drugs 2014 45 3071-3073 Nitrogenous chemical constituents from Carthamus tinctorius HONG Kui, XIE Xue, WANG Xue-jing, LIU Jun-chao, HUANG Wen-zhe, WANG Zhen-zhong, XIAO Wei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . É«°±Ëá ÏàËÆ¶È:78.5% Chinese Traditional and Herbal Drugs 2011 42 2186-2188 Chemical constituents in water fraction of Abelmoschus esculentus JIA, Lu, ZHONG, Li-jun, LI, Huan-fen, JING, Lin-lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . L-tryptophan ÏàËÆ¶È:78.5% Chinese Traditional and Herbal Drugs 2013 44 2803-2807 Chemical constituents from leaves of Datura metel (I) YANG Bing-you, LI Ting, GUO Rui, WANG Qiu-hong, KUANG Hai-xue Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . tryptophane ÏàËÆ¶È:78.5% Drugs & Clinic 2009 24 34-36 Chemical constituents from fruit of Broussonetia papyrifera XIONG Shan, CHEN Yu-wu, YE Zu-guang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . L-tryptophan ÏàËÆ¶È:78.5% Journal of Jinan University (Natural Science) 2011 32 304-306 Chemical constituents from the seeds of Hovenia acerba XU Fang-Fang, FAN Chun-Lin, WANG Lei, WANG Guo-Cai, ZHANG Xiao-Qi, YE Wen-Cai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . L-tryptophan ÏàËÆ¶È:78.5% Chinese Joumal of Experimental Traditional Medical Fomulae 2013 19 148-151 Chemical Constituents of Trigonella foenum-graecum LI Xiu-ru, DAN Xiao-mei, DAI Yu, WU Cheng-li, LI Hong-xiang, DENG Yun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . tryptophan ÏàËÆ¶È:78.5% Natural Product Sciences 2014 20 86-90 Phytochemical Constituents of the Leaves of Hosta longipes† Chung Sub Kim, Ki Hyun Kim, and Kang Ro Lee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . (R,S)-N-(phenylmethyl)-¦Á-[(trifluoroacetyl)amino]-1H-indole-3-propanamide C20H18F3N3O2 ÏàËÆ¶È:72.2% Journal of Medicinal Chemistry 1994 37 598-609 Tyrosine kinase inhibitors. 2. Synthesis of 2,2'-dithiobis(1H-indole-3-alkanamides) and investigation of their inhibitory activity against epidermal growth factor receptor and pp60v-src protein tyrosine kinases Andrew M. Thompson, David W. Fry, Alan J. Kraker, William A. Denny Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . (N2',N2'-Dimethyl-L-phenylalanyl)-L-tryptophan ÏàËÆ¶È:72.2% Helvetica Chimica Acta 1994 77 1999-2006 Almazole C, a New Indole Alkaloid Bearing an Unusually 2,5-Disubstituted Oxazole Moiety, and its putative biogenetic peptidic precursors, from a senegalese delesseriacean seaweed Graziano Guella, Ines Mancini and Francesco Pietra Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . N-Malonyl-L-tryptophan ÏàËÆ¶È:71.4% Phytochemistry 1992 31 823-826 N-acylamino acids from Ephedra distachya cultures Kyung-Sik Song, Yoshifumi Ishikawa, Shigeo Kobayashi, Ushio Sankawa, Yutaka Ebizuka Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . tryptophan ÏàËÆ¶È:71.4% Journal of Shenyang Pharmaceutical University 2010 27 69-74 Isolation and identification of metabolites from amarine bacterial strain Bacillus sp. GAO Hao, CHEN Guo-dong, TANG Jin-shan, ZHANG Shu-dan, WANG Nai-li, YAO Xin-sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . phenyl-2-bis-indolylmethane C23H18N2 ÏàËÆ¶È:71.4% The Journal of Antibiotics 2010 63 303-308 Aqabamycins A¨CG: novel nitro maleimides from a marine Vibrio species: II. Structure elucidation* Clarisse Blandine Fotso Fondja Yao, Wael Al Zereini, Serge Fotso, Heidrun Anke and Hartmut Laatsch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-04-30 08:02:26













»Ø¸´´ËÂ¥