| ²é¿´: 218 | »Ø¸´: 2 | ||
ÄÄ¡¢Aloneгæ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
|
13C NMR (101 MHz, MeOD) ¦Ä 66.24, 112.92, 114.82, 122.63, 123.26, 124.34, 126.88, 133.98,138.16,195.93. лл£¡ |
» ²ÂÄãϲ»¶
285Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600²ÄÁÏÓ뻯¹¤301·ÖÇóµ÷¼ÁԺУ
ÒѾÓÐ19È˻ظ´
277¹¤¿ÆÇóµ÷¼Á
ÒѾÓÐ11È˻ظ´
277Çóµ÷¼Á ÊýÒ»104·Ö
ÒѾÓÐ13È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
336Çóµ÷¼Á£¬Ò»Ö¾Ô¸Öпƴó
ÒѾÓÐ6È˻ظ´
071000ÉúÎïѧ£¬Ò»Ö¾Ô¸ÉîÛÚ´óѧ296·Ö£¬Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ19È˻ظ´
274Çóµ÷¼ÁÇóµ÷¼Á
ÒѾÓÐ7È˻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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
À±±ÊvСÐÂ: ½ð±Ò+2, ¹ÄÀøÓ¦Öú 2013-12-11 18:18:38
ÄÄ¡¢Alone: ½ð±Ò+5, ¡ï¡ï¡ïºÜÓаïÖú 2013-12-12 09:14:31
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
À±±ÊvСÐÂ: ½ð±Ò+2, ¹ÄÀøÓ¦Öú 2013-12-11 18:18:38
ÄÄ¡¢Alone: ½ð±Ò+5, ¡ï¡ï¡ïºÜÓаïÖú 2013-12-12 09:14:31
|
²éѯ½á¹û£º¹²²éµ½459¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 1H-indole-3-hydroxyacetyl ÏàËÆ¶È:100% Biochemical Systematics and Ecology 2012 43 210-213 Monoindole alkaloids from a marine sponge Mycale fibrexilis Ru-Ping Wang, Hou-Wen Lin, Ling-Zhi Li, Pin-Yi Gao, Ying Xu, Shao-Jiang Song Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3-hydroxylacetyl-indole C10H9NO2 ÏàËÆ¶È:100% Academic Journal of Second Military Medical University 2008 29 1234-1238 Isolation,identification and biological characterization of secondary metabolites produced by a marine Bacillus subtilis HAN Wen-ju, LU Xiao-ling, XU Qiang-zhi, LIU Xiao-yu, JIAO Bing-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-(Hydroxyucetyl) indole C10H9NO2 ÏàËÆ¶È:100% European Journal of Organic Chemistry 1996 1996 49-53 Antibiotics from Gliding Bacteria, LXXIII Indole and Quinoline Derivatives as Metabolites of Tryptophan in Myxobacteria Bettina Böhlendorf, Norbert Bedorf, Rolf Jansen, Wolfram Trowitzsch-Kienast, Gerhard Höfle, Edgar Forche, Klaus Gerth, Herbert Irschik, Brigitte Kunze and Hans Reichenbach Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3-(Hydroxy-acetyl)-1H-indole C10H9NO2 ÏàËÆ¶È:100% Natural Product Research and Development 2012 24 427-431 Chemical Constituents from Inula hupehensis ZHANG Fei; QIN Jiang-jiang; CHENG Xiang-rong; JIN Hui-zi; ZHANG Wei-dong Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-(Hydroxylacetyl)-indol C10H9NO2 ÏàËÆ¶È:90% Journal of Natural Products 1991 Vol 54 1056 Aromatic Secondary Metabolites from the Sponge Tedania ignis Rhonda L. Dillman, John H. Cardellina II. Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 3-(hydroxyacetyl)indole ÏàËÆ¶È:90% Phytochemistry 1990 29 3697-3698 3-(Hydroxyacetyl)indole,a plant growth regulator from the oregon red alga Prionitis lanceolata Matthew Bernart,William H. Gerwick Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-(hydroxylacetyl)-indole ÏàËÆ¶È:90% Chinese Journal of Natural Medicines 2004 2 88-90 Studies on Chemical Constituents of the Marine Sponge Biemna sp. from the South China Sea YAN Xiao-Hong; HOU Hui-Xin; GUO Yue-Wei Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3-hydroxyacetylindole C10H9NO2 ÏàËÆ¶È:90% Molecules 2012 17 11146-11155 Antitrypanosomal Alkaloids from the Marine Bacterium Bacillus pumilus Sergio Mart¨ªnez-Luis, Jos¨¦ F¨¦lix G¨®mez, Carmenza Spadafora, H¨¦ctor M. Guzm¨¢n and Marcelino Guti¨¦rrez Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3-hydroxyacetylindole C10H9NO2 ÏàËÆ¶È:90% Chinese Traditional and Herbal Drugs 2013 44 1241-1244 Chemical constituents from fruits of Euodia rutaecarpa WANG Xiao-xia, GAO Hui-yuan, JIANG Yong, ZHAO Ming-bo, WU Li-jun, TU Peng-fei Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 1-(3-indolyl)-2,3-dihydroxy-propan-1-one ÏàËÆ¶È:81.8% The Journal of Antibiotics 1995 48 522-524 Biosynthetic Capacities of Actinomycetes. 3 Naphthgeranine F, a Minor Congener of the Naphthgeranine Group Produced by Streptomyces violaceus CORINNA VOLKMANN, UWE HART JEN, AXEL ZEECK, HANS-PETER FIEDLER Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . methylindole-3-carboxylate ÏàËÆ¶È:80% Journal of Agricultural and Food Chemistry 2000 48 4687-4692 Isolation and Characterization of Fungal Inhibitors from Epichloë festucae Qin Yue, Christina J. Miller, James F. White, Jr., and Michael D. Richardson Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 3-(Bromoacetyl)-1H-indole ÏàËÆ¶È:80% 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 ̼Æ×Ä£Äâͼ 13 . 1,2-bis(1H-indol-3-yl)ethane-1,2-dione C18H12N2O2 ÏàËÆ¶È:70% Journal of Natural Products 2002 65 595-597 1,2-Bis(1H-indol-3-yl)ethane-1,2-dione, an Indole Alkaloid from the Marine Sponge Smenospongia sp. Matthew J. McKay, Anthony R. Carroll, Ronald J. Quinn, and John N. A. Hooper Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . N-(1-(5-Chloro-1H-indol-3-yl)ethyl)hydroxylamine ÏàËÆ¶È:70% Bioorganic & Medicinal Chemistry 2011 19 3204-3215 Synthesis and evaluation of 1-(1H-indol-3-yl)ethanamine derivatives as new antibacterial agents Olga N. Burchak,Emmanuelle Le Pihive, Laure Maigre, Xavier Guinchard , Pascale Bouhours ,Claude Jolivalt, Dominique Schneider , Max Maurin , Carmela Giglione , Thierry Meinnel ,Jean-Marc Paris , Jean-Noël Denis Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 1H-indole-3-carboxylic acid ÏàËÆ¶È:70% Chinese Journal of Medicinal Chemistry 2009 19 273-275 Chemical constituents in the leaves of Baphicacanthus cusia(Nees) Bremek. LIU Yuan, OU Yang-fu, YU Hai-yang, LI Ling, WANG Nai-li, YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . indole-3-carboxylic acid ÏàËÆ¶È:70% 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 ̼Æ×Ä£Äâͼ 17 . indole acid ÏàËÆ¶È:70% Chinese Traditional and Herbal Drugs 2013 44 269-271 Chemical constituents in Yi Medicine Blaps japonensis and their cytotoxic activities YAN Yong-ming, DONG Xiao-ping, LI Yan, CHENG Yong-xian Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Indol-3-carboxylic acid C9H7O2N ÏàËÆ¶È:70% Natural Product Communications 2013 8 1245-1246 Chemical Constituents of the Leaves of Triumfetta semitriloba Alejandra Barraza-Morales, Deisy Medrano-Nahuat, Sergio R. Peraza-S¨¢nchez Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . indole-3-carboxylic acid ÏàËÆ¶È:70% Journal of Shenyang Pharmaceutical University 2012 29 337-339 Isolation and identification of chemical constituents from leaves of Gynura procumbens(Lour.)Merr. ZHANG Ying; JIANG Kun; YANG Li-jun; TAN Jun-jie; MENG Da-li; TAN Chang-heng Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-12-11 16:57:15
ÄÄ¡¢Alone
гæ (³õÈëÎÄ̳)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 505.5
- Ìû×Ó: 25
- ÔÚÏß: 5.8Сʱ
- ³æºÅ: 2850592
- ×¢²á: 2013-12-05
3Â¥2013-12-12 09:14:43














»Ø¸´´ËÂ¥