| ²é¿´: 206 | »Ø¸´: 1 | ||
zhiwu1983ľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý ÒÑÓÐ1È˲ÎÓë
|
| ̼Æ×Êý¾ÝÈçÏ£º12.0,12.1,14.3,19.0,19.1,19.2,20.0,21.4,22.8,23.2,25.8,26.2,28.6,29.3,31.8,34.1,36.2,36.6,37.1,37.3,39.8,42.2,43.0,46.0,48.6,55.0,55.7,56.6,71.7,82.1,121.7,144.1 |
» 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´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬¸ø30J
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
Çó΢Æ×Êý¾Ý лл
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
Çó´óϺ²é΢Æ×£¬Íò·Ö¸Ðл°¡£¡£¡£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
ÇóÈË΢Æ×²éѯ£¬¼±£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
΢Æ×²é½á¹¹£¬ÓÐÆ×ͼ
ÒѾÓÐ3È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´

ÓÐËù²»Îª
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 304 (´óѧÉú)
- ½ð±Ò: 9684.2
- É¢½ð: 16
- ºì»¨: 14
- Ìû×Ó: 1106
- ÔÚÏß: 814.3Сʱ
- ³æºÅ: 481441
- ×¢²á: 2007-12-17
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhiwu1983: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-12-12 22:08:56
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhiwu1983: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-12-12 22:08:56
|
²éѯ½á¹û£º¹²²éµ½14076¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . schleicheol 1 C30H52O2 ÏàËÆ¶È:93.7% Journal of Natural Products 2000 63 72-78 Isolation and Structures of Schleicherastatins 1-7 and Schleicheols 1 and 2 from the Teak Forest Medicinal Tree Schleichera oleosa1 George R. Pettit,Atsushi Numata, Gordon M. Cragg, Delbert L. Herald, Tamie Takada,Chika Iwamoto,Roland Riesen, Jean M. Schmidt, Dennis L. Doubek, and Animesh Goswami Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (24S)-stigmast-5-en-7¦Â-ethoxy-3¦Â-ol C31H54O2 ÏàËÆ¶È:87.5% Journal of Asian Natural Products Research 2005 7 165-169 Sterols from the pericarp of Sphaerophysa salsula DC GUO-YU LI, JIN-HUI WANG and XIAN LI Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 7¦Â-methoxy-sigmast-5-en-3¦Â-ol ÏàËÆ¶È:84.3% China Journal of Chinese Materia Medica 2008 33 1035-1038 Study on Steroids of Cacalia tangutica LIU Qing, LIU Zhenling, TIAN Xuan Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (3¦Â,7¦Á)-7-Methoxystigmast-5-en-3-ol C30H52O2 ÏàËÆ¶È:84.3% Chemistry & Biodiversity 2012 9 567-576 Antifeedant Activity of Fatty Acid Esters and Phytosterols from Echium wildpretii Omar Santana, Matias Reina, Braulio M. Fraga, Jes¨²s Sanz and Azucena Gonza¡älez-Coloma Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . schleicheol 2 C30H52O2 ÏàËÆ¶È:81.2% Journal of Natural Products 2000 63 72-78 Isolation and Structures of Schleicherastatins 1-7 and Schleicheols 1 and 2 from the Teak Forest Medicinal Tree Schleichera oleosa1 George R. Pettit,Atsushi Numata, Gordon M. Cragg, Delbert L. Herald, Tamie Takada,Chika Iwamoto,Roland Riesen, Jean M. Schmidt, Dennis L. Doubek, and Animesh Goswami Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 7¦Â-hydroxysitosterol ÏàËÆ¶È:81.2% Acta Botanica Boreali-Occidentalia Sinica 2009 29 1898-1903 Chemical Components of Glechoma biondiana XU Jing, WEI Ping-zhi, LIU Zhen-ling, TIAN Xuan Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 7¦Â-Hydroxysitosterol C29H50O2 ÏàËÆ¶È:81.2% Journal of Chinese Pharmaceutical Sciences 2007 16 288-293 Chemical constituents of the flower buds of Tussilago farfara Yu-Feng Liu; Xiu-Wei Yang and Bin Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 7¦Â-hydroxysitosterol C29H50O2 ÏàËÆ¶È:81.2% Steroids 2005 70 886-895 Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Stigmast-5-ene-3¦Â,7¦Á-diol ÏàËÆ¶È:81.2% Journal of Asian Natural Products Research 2005 7 165-169 Sterols from the pericarp of Sphaerophysa salsula DC GUO-YU LI, JIN-HUI WANG and XIAN LI Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Stigmast-5-ene-3¦Â,7¦Â-diol ÏàËÆ¶È:81.2% Journal of Asian Natural Products Research 2005 7 165-169 Sterols from the pericarp of Sphaerophysa salsula DC GUO-YU LI, JIN-HUI WANG and XIAN LI Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 7¦Â-hydroxysitosterol ÏàËÆ¶È:81.2% China Journal of Chinese Materia Medica 2008 33 1566-1570 Studies on chemical constituents from stem bark of Trwia nudiflora WU Shaohua, SHENG Yuemao, CHEN Youwei, YANG Liyuan, LI Shaolan, LI Zhiying Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 7¦Â-hydroxysitosterol C29H50O2 ÏàËÆ¶È:81.2% Journal of Natural Products 1987 Vol 50 881 Sterols and Steryl Glycosides from Urtica dioica Neera Chaurasia, Max Wichtl Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 7¦Â-hydroxysitosterol ÏàËÆ¶È:81.2% Journal of Natural Products 1990 Vol 53 1430 Stigmasterols from Typha latifolia Marina Della Greca, Pietro Monaco, Lucio Previtera Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 7¦Á-hydroxysitosterol ÏàËÆ¶È:81.2% Journal of Natural Products 1990 Vol 53 1430 Stigmasterols from Typha latifolia Marina Della Greca, Pietro Monaco, Lucio Previtera Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . stigmast-5-ene-3¦Â,7¦Â-diol ÏàËÆ¶È:81.2% Chemical Research in Chinese Universities 1997 13 378-381 Two New Sterols f rom Adenophora Stenanthina Subsp. Xif engensis HOU Zhen-fu, SHI Yan-ping, MEI Shuang-x i and LI Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . stigmast-5-en-3¦Â,7¦Â-diol ÏàËÆ¶È:81.2% China Journal of Chinese Materia Medica 2011 Vol 36,Issue 7 891-895 Chemical constituents from petroleum ether portion of Abelmoschus esculentus JIA Lu, GUO M ingm ing, LI Dong, JING Lin lin Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 7¦Â-hydroxysitosterol ÏàËÆ¶È:81.2% Chinese Traditional and Herbal Drugs 2010 41 187-190 Studies on chemical constituents of Oxytropis kansuensis GONG Hong-fei; YANG Ai-mei; LIU Jun-xi; DI Duo-long Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 7¦Â-hydroxysitosterol ÏàËÆ¶È:81.2% Chinese Journal of Natural Medicines 2007 5 105-107 Chemical Constituents of African Plant Harpagophytum procumbens QI Jin; CHEN Ji-Jun; TU Ying; CHEN Lu; YU Bo-Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . stigmast-5-ene-3¦Â,7¦Á-diol ÏàËÆ¶È:81.2% Chinese Journal of Natural Medicines 2010 8 267-269 Steroids and Phenols from Sonchus arvensis XIA Zheng-Xiang; LIANG Jing-Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . stigmast-5-ene-3¦Â,7¦Â-diol ÏàËÆ¶È:81.2% Pharmazie 2002 57 209-211 Two new steroids from Adenophora stenanthina subsp. xifengensis Zhen-Fu Hou - Yong-Qiang Tu - Yu Li Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . stigmast-5-en-3¦Â,7¦Á-diol ÏàËÆ¶È:81.2% Pharmazie 2005 60 464-467 Steroids from Saussurea ussuriensis Jia-Tao Feng and Yan-Ping Shi Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-12-12 21:17:57














»Ø¸´´ËÂ¥