| ²é¿´: 280 | »Ø¸´: 1 | ||
zengjundeyo½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
Çó΢Æ×Êý¾ÝèÃÒ»¸öÉúÎï¼î
|
| 13.2,22.1,34.9,42.3,50.8,52.2,53.3,56.1,61.3,63.5,107.8,112.0,118.6,119.1,119.8,122.0,128.3,135.2,135.9,138.1,176.1 |
» ²ÂÄãϲ»¶
307·Ö²ÄÁÏרҵÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
336Çóµ÷¼Á£¬Ò»Ö¾Ô¸Öпƴó
ÒѾÓÐ9È˻ظ´
Çóµ÷¼Á Ò»Ö¾Ô¸Î÷ÄϽ»Í¨´óѧ085701»·¾³¹¤³Ì 282·Ö
ÒѾÓÐ15È˻ظ´
»¯Ñ§¹¤³Ìµ÷¼Á289
ÒѾÓÐ24È˻ظ´
284Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
275 Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
²ÄÁϹ¤³Ì322
ÒѾÓÐ16È˻ظ´
»¯¹¤Ñ§Ë¶ 285Çóµ÷¼Á
ÒѾÓÐ24È˻ظ´
293µ÷¼Á
ÒѾÓÐ18È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÒ»¸öÉúÎï¼î»¯ºÏÎï΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖú3¸ö΢Æ×Êý¾Ý
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ivyasspring
½ð³æ (СÓÐÃûÆø)
- Ó¦Öú: 46 (СѧÉú)
- ½ð±Ò: 1023.6
- ºì»¨: 5
- Ìû×Ó: 152
- ÔÚÏß: 39.8Сʱ
- ³æºÅ: 1764251
- ×¢²á: 2012-04-18
- ÐÔ±ð: MM
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zengjundeyo: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-04-26 09:26:05
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zengjundeyo: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-04-26 09:26:05
|
1 . amsosinine C21H26N2O4 ÏàËÆ¶È:71.4% Planta Medica 1991 57 566-568 New Indole Alkaloids from Amsonia sinensis Hong-MeiLiu, Bin Wu,Qi-TaiZheng,and Xiao-ZhangFeng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . compound 1 C21H26N2O4 ÏàËÆ¶È:71.4% Chinese Chemical Letters 1991 2 297-298 AMSOSININE.A NEW INDOLE ALKALOID FROM AMSONIA SINENSIS HONG MEI LIU,XIAO ZHANG FENG,DIN WU AND QI TAI ZHENG Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . amsosinine ÏàËÆ¶È:71.4% Chinese Traditional and Herbal Drugs 2003 34 390-392 Studies on chemical constituents of Amsonia sinensis WANG Ai-guo; FENG Xiao-zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . yohimbine ÏàËÆ¶È:66.6% Journal of Natural Products 2001 64 193-195 Hydroxylation of Yohimbine in Superacidic Media: One-Step Access to Human Metabolites 10 and 11-Hydroxyyohimbine Alain Duflos,Florence Redoules,Jacques Fahy, Jean-Claude Jacquesy, and Marie-Paule Jouannetaud Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . ¦Â-yohimbine ÏàËÆ¶È:66.6% Journal of Natural Products 1983 Vol 46 708-722 Aspidosperma de Guyane: Alcaloïdes des Graines de Aspidosperma oblongum G. M. T. Robert, A. Ahond, C. Poupat, P. Potier, H. Jacquemin, S. K. Kan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . ajmalicidine ÏàËÆ¶È:66.6% Planta Medica 1994 60 480-481 On the Structure of the Indole Alkaloid Ajmalicidine Lounasmaa, M.; Tolvanen, A. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . ajmalicinine ÏàËÆ¶È:66.6% Planta Medica 1994 60 480-481 On the Structure of the Indole Alkaloid Ajmalicidine Lounasmaa, M.; Tolvanen, A. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . pleiocarpamine C20H22N2O2 ÏàËÆ¶È:66.6% Phytochemistry 1990 29 3377-3379 17¦Á-O-Methylyohimbine and vallesiachotamine from roots ofAmsonia elliptica Martina Sauerwein,Koichiro Shimomura Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . methyl (1S,2R,12br)-2-propyl-1,2,3,4,6,7,12,12b-octahydroind-olo[2,3-a]quinolizine-1-carboxylate C20H26N2O2 ÏàËÆ¶È:66.6% European Journal of Organic Chemistry 2011 6755-6763 Organocatalyzed Cascade Reactions of Cyclic ¦Â-Enamino Esters and ,¦Â-Unsaturated Aldehydes Leading to Indoloquinolizidines and Benzoquinolizidines Xiaoyu Wu, Linlin Nie, Huihui Fang, Jie Chen, Weiguo Cao and Gang Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (-)-3R-Methoxycoronaridine ÏàËÆ¶È:63.6% Phytochemistry 1994 37 1729-1735 Indole alkaloids and terpenoids fromTabernaemontana markgrafiana Helene B. Nielsen, Alan Hazell, Rita Hazell, Felipe Ghia, Kurt B.G. Torssell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . compound 6 ÏàËÆ¶È:63.6% Phytochemistry 1987 26 833-836 Quaternary alkaloids from Peschiera fuchsiaefolia Raquel M. Braga,Francisco De A.M. Reis Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 17¦Á-O-methylyohimbine ÏàËÆ¶È:63.6% Phytochemistry 1990 29 3377-3379 17¦Á-O-Methylyohimbine and vallesiachotamine from roots ofAmsonia elliptica Martina Sauerwein,Koichiro Shimomura Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . Villocarine A C22H26N2O3 ÏàËÆ¶È:63.6% Bioorganic & Medicinal Chemistry 2011 19 4075-4079 New vasorelaxant indole alkaloids, villocarines A¨CD from Uncaria villosa Hirotaka Matsuo, Ryuichi Okamoto, Kazumasa Zaima, Yusuke Hirasawa, Intan Safinar Ismail, Nordin Hj Lajis, Hiroshi Morita Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . yohimbinic acid C20H26N2O3 ÏàËÆ¶È:61.9% Journal of Natural Products 2005 68 848-852 Indole Alkaloids and Other Constituents of Rauwolfia serpentina Atsuko Itoh, Tomoko Kumashiro, Machiko Yamaguchi, Naotaka Nagakura, Yoshiyuki Mizushina, Toyoyuki Nishi, and Takao Tanahashi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . corynanthine C21H25N2O3 ÏàËÆ¶È:61.9% Planta Medica 2000 66 531-536 Leishmanicidal,Antiplasmodial and Cytotoxic Activity of Indole Alkaloids from Corynanthe pachyceras Dan Stærk,Else Lemmich,Jette Christensen, Arsalan Kharazmi,Carl Erik Olsen,Jerzy W.Jaroszewski Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . dihydrocorynantheine C22H29N2O3 ÏàËÆ¶È:61.9% Planta Medica 2000 66 531-536 Leishmanicidal,Antiplasmodial and Cytotoxic Activity of Indole Alkaloids from Corynanthe pachyceras Dan Stærk,Else Lemmich,Jette Christensen, Arsalan Kharazmi,Carl Erik Olsen,Jerzy W.Jaroszewski Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . dihydrocorynantheol ÏàËÆ¶È:61.9% Journal of Natural Products 1983 Vol 46 694-707 Aspidosperma de Guyane: Alcaloïdes de Aspidosperma marcgravianum G. M. T. Robert, A. Ahond, C. Poupat, P. Potier, C. Joll¨¨s, A. Jousselin, H. Jacquemin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . epi-yohimbol ÏàËÆ¶È:61.9% Journal of Natural Products 1994 Vol 57 287 Indole Alkaloids from Antirhea portoricensis Bernard Weniger, Robert Anton, Teresa Varea, Jean-Charles Quirion, Jaume Bastida, Ricardo Garcia Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (16R)-E-Iso-sitsirikine ÏàËÆ¶È:61.9% Journal of Natural Products 1995 Vol 58 131-133 The Rhazimanine-Bhimberine Enigma Mauri Lounasmaa, Reija Jokela, Pirjo Hanhinen, Jari Miettinen, Jaana Salo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 19E-16R-isositsirikine ÏàËÆ¶È:61.9% Phytochemistry 1994 37 1729-1735 Indole alkaloids and terpenoids fromTabernaemontana markgrafiana Helene B. Nielsen, Alan Hazell, Rita Hazell, Felipe Ghia, Kurt B.G. Torssell Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-04-26 09:21:59














»Ø¸´´ËÂ¥