| ²é¿´: 251 | »Ø¸´: 1 | ||
ÂÌË®ÏÐÖñľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
άÆÕÇóÖú£¬¼±Ðè ÒÑÓÐ1È˲ÎÓë
|
| ¼×´¼£º111.5,120.6,120.9,122.2,126.2,131.9,136.8 |
» ²ÂÄãϲ»¶
»¯Ñ§¹¤³ÌÓë¼¼Êõ324µ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸211µç×ÓÐÅÏ¢347Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
²ÄÁÏÓ뻯¹¤300Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
0856ר˶Çóµ÷¼Á Ï£ÍûÊÇaÇøÔºÐ£
ÒѾÓÐ8È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
±¾¿ÆÎ÷¹¤´ó 0856 324Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
µ÷¼Á
ÒѾÓÐ8È˻ظ´
314Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ19È˻ظ´
277 ÊýÒ»104£¬Ñ§Ë¶£¬Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
άÆÕÇóÖú£¡Ð»Ð»~
ÒѾÓÐ3È˻ظ´
̼Æ×ÇóÖú ¼±ÓÃ
ÒѾÓÐ3È˻ظ´
άÆÕÇóÖú£¬Ð»Ð»£¡£¡
ÒѾÓÐ3È˻ظ´
European Journal of Wood and Wood Products
ÒѾÓÐ3È˻ظ´
ÇóÖú¹ØÓÚ¾Û°±õ¥µ¯ÐÔÌåºÏ³ÉÖеÄһЩÎÊÌ⣬¼±ÐèʦÐÖʦ½ãÃǽâ´ð¡¡
ÒѾÓÐ16È˻ظ´
άÆÕÊý¾ÝÇóÖúX
ÒѾÓÐ3È˻ظ´
Çó¡¶Ã¢ÖÖ¡·ÔÓÖ¾¹Ù·½Í¶¸å·½Ê½£¨¾Ü¾øÖн飩£¡£¡£¡
ÒѾÓÐ3È˻ظ´
¼±ÐèάÆÕ̼Æ×¼ìË÷£¬¼±Óã¡Ð»Ð»´ó¼Ò°ïæ
ÒѾÓÐ5È˻ظ´
ÇóÖú¾Û°±õ¥·½ÃæµÄÊé¼®ºÍ²ÄÁÏ ¼±Ð裬лл¸÷λ´óÏÀ
ÒѾÓÐ3È˻ظ´
RUSSIAN CHEMICAL BULLETIN
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿¼±Ðè×öITO·ÛÄ©ºÍ°Ð²Ä·½ÃæµÄ×ÊÁÏ£¡Ê®·Ö¸Ðл£¡
ÒѾÓÐ13È˻ظ´
¡¾ÇóÖú¡¿¼±ÐèÖпÆÔºÖ²Îïѧ¿¼²©×¨Òµ¿ÎÕæÌâ»ò¸´Ï°×ÊÁÏ
ÒѾÓÐ7È˻ظ´
¡¾ÇóÖú¡¿ÇóÖúchem3D½Ì³Ì£¬¼±Ðè°¡£¬ÓеĴ«ÎÒÒ»·Ý£¬Ð»Ð»À²
ÒѾÓÐ3È˻ظ´
¡¾ÇóÖú¡¿¼±Ðè¡¶¸ß·Ö×Óͨ±¨¡·ÔÓÖ¾µÄͶ¸å¸ñʽҪÇó£¬Ð»Ð»
ÒѾÓÐ6È˻ظ´
¡¾ÇóÖú¡¿¼±Ðèstep by step2000£¨1-4²á£©Ñ§ÉúÓÃÊéµÄword°æ
ÒѾÓÐ7È˻ظ´
¡¾ÇóÖú¡¿¼±ÐèCompad Visual Fortran 6.6
ÒѾÓÐ9È˻ظ´

seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48419.9
- ºì»¨: 52
- Ìû×Ó: 6747
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÂÌË®ÏÐÖñ: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-16 21:14:49
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÂÌË®ÏÐÖñ: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-16 21:14:49
|
1 . 1H-ßÅßò C7H6N2 ÏàËÆ¶È:100% Asia-Pacific Traditional Medicine 2013 9 47-48 ´óÀöÂÖУ¾ú´Î¼¶´úл²úÎïÑо¿ CUI Xiu-chun, LUO Du-qiang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 1H-ßÅßá-2-ôÈËá ÏàËÆ¶È:87.5% Modern Chinese Medicine 2008 10(12) 29-31 Studies on the Metabolites of Salvianolic Acid B Yuan Zheng, Li Guoyu, , Zeng Yimei, Wang Jinhui Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 1H-indole-3-carboxylicacid ÏàËÆ¶È:77.7% China Journal of Chinese Materia Medica 2009 34 994-998 Chemical constituents of A lisma orientalis and their immunosuppressive function ZHANG Chaofeng, ZHOU Aichun, ZHANG mian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . bis(3-indolyl) ketone C17H12N2O ÏàËÆ¶È:77.7% Heterocycles 2004 63 2371-2377 Effect of Sodium Naphthalenide, a Key Set Reagent, on 3-Substituted Indoles Avijit Banerji*, Debasish Bandyopadhyay, and Bidyut Basak Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . indolyl-3-carboxylic acid C9H7NO2 ÏàËÆ¶È:77.7% Chinese Traditional and Herbal Drugs 2010 41 870-873 Áõ¼ÄÅ«µÄ»¯Ñ§³É·ÖÑо¿ Î¾§;Ê·º£Ã÷;êÃçæ;ÁõÑÞ·¼;ÖÜÓêºç;³ÂÓñƽ;ÍÀÅô·É Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . indole-3-carboxylic acid ÏàËÆ¶È:77.7% The Journal of Antibiotics 2001 54 628-634 TMC-205 a New Transcriptional Up-Regulator of SV40 Promoter Produced by an Unidentified Fungus. Fermentation, Isolation, Physico-chemical Properties, Structure Determination and Biological Activities MASAAKI SAKURAI,JUN KOHNO,MAKI NISHIO,KOZO YAMAMOTO,TORU OKUDA,KIMIO KAWANO and NORIYUKI NAKANISHI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . indole-3-carboxylic acid ÏàËÆ¶È:77.7% Zeitschrift f¨¹r Naturforschung C 2011 66 485-490 Effects of Indole Amides on Lettuce and Onion Germination and Growth T. F. Borgati and M. A. D. Boaventura Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . indole-3-carboxylic acid C9H7NO2 ÏàËÆ¶È:77.7% Plant Diversity and Resources 2012 34 101-106 New Withanolides from Nicandra physaloides (Solanaceae) YI Qian-Kun, LI Bo, LIU Ji-Kai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . indole-3-carboxylic acid ÏàËÆ¶È:77.7% The Journal of Organic Chemistry 1996 61 6591-6593 Arthrichitin. A New Cell Wall Active Metabolite from Arthrinium phaeospermum E. K. S. Vijayakumar, Kirity Roy, Sugata Chatterjee, S. K. Deshmukh, and B. N. Ganguli Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . indole-3-carboxylic acid C9H7NO2 ÏàËÆ¶È:77.7% Natural Product Research 2013 27 1366-1371 A new 20-membered macrolide produced by a marine-derived Micromonospora strain Peng Fei, Wang Chuan-xi, Xie Yang, Jiang Hong-lei, Chen Lu-jie, Paulina Uribe, Alan T. Bull, Michael Goodfellow, Jiang Hong & Lian Yun-yang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . indole-3-carboxylic acid ÏàËÆ¶È:77.7% Chinese Traditional and Herbal Drugs 2014 45 631-634 Chemical constituents from seeds of Helianthus annuus FEI Yong-he, CHEN Zhong, LI Xiao-ran, XU Qiong-ming, YANG Shi-lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . ¦Â-indole carboxylic acid ÏàËÆ¶È:77.7% Military Medical Sciences 2013 37 279-282 Chemical constituents from Solanum lyratum Thunb£®£¨¢ò£© YIN Hai-long, LI Jian, DONG Jun-xing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . ßÅßá-3-¼×Ëá ÏàËÆ¶È:77.7% Chinese Journal of Medicinal Chemistry 2012 22 38-43 Chemical constituents from the endophyte Bacillus pumilus derived from Breynia fruticosa HUO Pei-yuan; CHEN Hua-hong; JIANG Yi; HAN Li; XU Li-hua; HUANG Xue-shi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . ¦Â-indole carboxylic acid ÏàËÆ¶È:77.7% Bulletin of the Academy of Military Medical Sciences 2013 37 279-282 Chemical constituents from Solanum lyratum Thunb. ( ¢ò) YIN Hai-long, LI Jian, DONG Jun-xing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-03-16 21:00:05













»Ø¸´´ËÂ¥