| ²é¿´: 218 | »Ø¸´: 1 | ||
wawlgchͳæ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾ÝÇóÖú
|
|
ÈܼÁÊÇCDCl3 20.69, 21.04,26.55, 27.33, 27.72,34.58,41.48,41.93,51.40, 57.22, 63.43,124.53, 137.39,165.72 |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
22408 266Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ43È˻ظ´
307Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
338Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
326·Ö£¬Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁÏ¿ÆÑ§Ó빤³Ì320Çóµ÷¼Á£¬080500
ÒѾÓÐ9È˻ظ´
0703»¯Ñ§µ÷¼Á 348·Ö
ÒѾÓÐ10È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
JYN-33 ΢Æ×ÇóÖú£¬¼±Çó£¬Ð»Ð»£¬×·¼Ó½ð±Ò¡£¡£¡£
ÒѾÓÐ6È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý3¸ö
ÒѾÓÐ6È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý~
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´

wangwang1989
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- Ó¦Öú: 525 (²©Ê¿)
- ½ð±Ò: 11769.2
- É¢½ð: 1451
- ºì»¨: 21
- ɳ·¢: 18
- Ìû×Ó: 4912
- ÔÚÏß: 315.2Сʱ
- ³æºÅ: 1467486
- ×¢²á: 2011-10-30
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
wawlgch: ½ð±Ò+15, ¡ïÓаïÖú 2013-07-11 21:55:48
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
wawlgch: ½ð±Ò+15, ¡ïÓаïÖú 2013-07-11 21:55:48
|
²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½146¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (-)-sophocarpine ÏàËÆ¶È:100% Natural Product Sciences 2001 7 5-8 Minor Constituents from the Roots of Sophora flavescens Kim, Ju-Sun; Han, Sang-Jun; Byun, Ji-Hye; Xu, Yong-Nan; Yoo, Sang-Woo; Kang, Sam-Sik; Son, Kun-Ho; Chang, Hyeun-Wook; Kim, Hyun-Pyo Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . sophocarpine ÏàËÆ¶È:93.3% China Journal of Chinese Materia Medica 2006 31 557-560 Constituents in the alkaloid fraction of Kushen decoction LIU Bin, SHI Rengbing Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (-)-sophocarpine ÏàËÆ¶È:93.3% Phytochemistry 1999 50 189-193 Lupin alkaloids from seeds of Sophora viciifolia Ping Xiao,Hajime Kubo,Hideaki Komiy¦Á, Kimio Higashiyam¦Á, Yu-ning Yan,Jia-shi Li , Shigeru Ohmiya Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (-)-sophocarpine C15H22N2O ÏàËÆ¶È:93.3% Bioorganic & Medicinal Chemistry Letters 2006 16 1231-1235 (+)-12¦Á-Hydroxysophocarpine, a new quinolizidine alkaloid and related anti-HBV alkaloids from Sophora flavescens Pei-Lan Ding, Zhi-Xin Liao, Hai Huang, Pei Zhou, Dao-Feng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (-)-sophocarpine ÏàËÆ¶È:93.3% Chinese Pharmaceutical Journal 2010 45 1451-1454 Studies on Chemical Constituents from Flowers of Sophora viciifolia Hance WEN Min, MA Yun-bao, MAO Xiao-jian, ZHANG Xue-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . sophorcarpine C15H22N2O ÏàËÆ¶È:80% Chemistry of Natural Compounds 1996 32 737-858 ALKALOIDS. PLANTS, STRUCTURES, PROPERTIES" Chapter 2, 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 7 . 9¦Á-hydroxysophocarpine C15H22N2O2 ÏàËÆ¶È:80% Phytochemistry 1999 50 189-193 Lupin alkaloids from seeds of Sophora viciifolia Ping Xiao,Hajime Kubo,Hideaki Komiy¦Á, Kimio Higashiyam¦Á, Yu-ning Yan,Jia-shi Li , Shigeru Ohmiya Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 9¦Á-hydroxysophocarpine C15H22N2O2 ÏàËÆ¶È:80% Phytochemistry 1999 50 189-193 Lupin alkaloids from seeds of Sophora viciifolia Ping Xiao,Hajime Kubo,Hideaki Komiy¦Á, Kimio Higashiyam¦Á, Yu-ning Yan,Jia-shi Li , Shigeru Ohmiya Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (-) 9¦Á-hydroxysophocarpine ÏàËÆ¶È:80% Chinese Pharmaceutical Journal 2010 45 1451-1454 Studies on Chemical Constituents from Flowers of Sophora viciifolia Hance WEN Min, MA Yun-bao, MAO Xiao-jian, ZHANG Xue-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . sophocarpine ÏàËÆ¶È:73.3% China Journal of Chinese Materia Medica 1997 22 741-743 Alkaloids in Sophora alopecuroides Seed and Relevant Tests for Activity Zhang Lanzhen and Li, P J Houghton and S Jackson, P R Twentyman Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Compound 5 C15H25N3O ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry Letters 2010 20 7537-7539 Synthesis and in vitro inhibitory activity of matrine derivatives towards pro-inflammatory cytokines Honggang Hu, Shaozhan Wang, Chunmei Zhang, Liang Wang, Li Ding, Junping Zhang, Qiuye Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . matrine C15H24N2O ÏàËÆ¶È:64.2% Chemistry of Natural Compounds 1996 32 596-675 ALKALOIDS. PLANTS, STRUCTURES, PROPERTIES" Chapter 2, 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 13 . (-)-14¦Â-hydroxymatrine C15H24N2O2 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1996 44 1951-1953 (-)-14¦Â-Hydroxymatrine, a New Lupine Alkaloid from the Roots of Sophora tonkinensis Ping XIAO,Jiashi LI,Hajime KUBO,Kazuki SAITO,Isamu MURAKOSHI and Shigeru OHMIYA Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (+)-matrine ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1996 44 1951-1953 (-)-14¦Â-Hydroxymatrine, a New Lupine Alkaloid from the Roots of Sophora tonkinensis Ping XIAO,Jiashi LI,Hajime KUBO,Kazuki SAITO,Isamu MURAKOSHI and Shigeru OHMIYA Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . matrine ÏàËÆ¶È:60% China Journal of Chinese Materia Medica 2006 31 557-560 Constituents in the alkaloid fraction of Kushen decoction LIU Bin, SHI Rengbing Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-07-11 21:47:10














»Ø¸´´ËÂ¥