| ²é¿´: 263 | »Ø¸´: 1 | ||
gyqqtbn01гæ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬Ð»Ð»ÒÑÓÐ1È˲ÎÓë
|
|
ë®´úÂÈ·Â 11.9,12.0,12.1,12.3,15.4,18.3,18.8,19.8,21.1,21.2,23.1,24.3,24.4,25.4,26.1,28.3,28.9,29.2,31.9,36.2,36.5,38.9,39.7,39.8,40.5,42.2,42.3,45.9,50.1,50.2,51.3,56.0,56.1,56.8,56.9,77.2,121.7,129.3,138.3,140.8 |
» ²ÂÄãϲ»¶
ÇëÎÊÓÐÆÀÖ°³Æ£¬°Ñ¿ÆÑнÌѧҵ¼¨Ëã·ÖÅÅÐòµÄ¸ßУÂð
ÒѾÓÐ6È˻ظ´
2025ÀäÞøÑ§Ê²Ã´Ê±ºò³ö½á¹û
ÒѾÓÐ6È˻ظ´
Bioresource TechnologyÆÚ¿¯£¬µÚÒ»´Î·µÐÞµÄʱºò±»Í˻غü¸´ÎÁË
ÒѾÓÐ7È˻ظ´
Õæ³ÏÇóÖú£ºÊÖÀïµÄÊ¡Éç¿ÆÏîÄ¿½áÏîÒªÇóÖ÷³ÖÈËһƪÖÐÎĺËÐÄ£¬ÓÐʲôÇþµÀÄÜ·¢ºËÐÄÂð
ÒѾÓÐ8È˻ظ´
ѰÇóÒ»ÖÖÄÜ¿¸×¡Ç¿Ñõ»¯ÐÔ¸¯Ê´ÐÔµÄÈÝÆ÷ÃÜ·â¼þ
ÒѾÓÐ5È˻ظ´
ÇëÎÊÄÄÀï¿ÉÒÔÓÐÇàBÉêÇëµÄ±¾×Ó¿ÉÒÔ½è¼øÒ»Ï¡£
ÒѾÓÐ4È˻ظ´
ÇëÎÊÏ´ó¼ÒΪʲôÕâ¸öÁåľżÁª¼¸ºõ²»·´Ó¦ÄØ
ÒѾÓÐ5È˻ظ´
Ìì½ò¹¤Òµ´óѧ֣Áø´ºÍŶӻ¶Ó»¯Ñ§»¯¹¤¡¢¸ß·Ö×Ó»¯Ñ§»òÓлúºÏ³É·½ÏòµÄ²©Ê¿ÉúºÍ˶ʿÉú¼ÓÈë
ÒѾÓÐ4È˻ظ´
¿µ¸´´óѧ̩ɽѧÕßÖÜì÷»ÝÍŶÓÕÐÊÕ²©Ê¿Ñо¿Éú
ÒѾÓÐ6È˻ظ´
AIÂÛÎÄд×÷¹¤¾ß£ºÊÇ¿ÆÑмÓËÙÆ÷»¹ÊÇѧÊõ×÷±×Æ÷£¿
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
ÇóÖúһ΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖú¡¢¡¢¡¢Ð»Ð»´óÉñ
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¡¼±£¡Ð»Ð»£¡
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú лл£¡
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»»¯ºÏÎï΢Æ×Êý¾Ý½á¹¹
ÒѾÓÐ10È˻ظ´
ÇóÖú»¯ºÏÎï΢Æ×ËÑË÷
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú13C΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
zhou_biao
ľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 416 (˶ʿ)
- ½ð±Ò: 2533
- É¢½ð: 1600
- ºì»¨: 7
- Ìû×Ó: 559
- ÔÚÏß: 178.4Сʱ
- ³æºÅ: 2963815
- ×¢²á: 2014-02-11
- רҵ: ÉúÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
gyqqtbn01: ½ð±Ò+10 2015-04-14 10:04:55
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
gyqqtbn01: ½ð±Ò+10 2015-04-14 10:04:55
|
1 . ¦Â-sitosterol and stigmasterol ÏàËÆ¶È:80% The Chinese Pharmaceutical Journal 2000 52 261-273 Studies on Anti-inflammatory Constituents of Leucas Mollissima WALL. var. Chinensis Benth ¹Åؑͥ(Chen-Ting Ku), ê?„ÙÖÇ(Sheng-Chih Chen), ÍõÀ^ƽ(Jih-Pyang Wang), …ǽðžI(Jin-Bin Wu), ¹ù„ÙÖú(Sheng-Chu Kuo) Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . mixture of ¦Â-sitosterol and stigmasterol ÏàËÆ¶È:75% The Chinese Pharmaceutical Journal 2003 55 109-119 Antiproliferative Constituents from Gynura divaricata subsp. formosana Sheng-Chih Chen*, Li-Ling Hong, Chung-Yang Chang, Chun-Jen Chen, Mei-Hua Hsu, Yuan-Chao Huang, Tai-Hung Huang and Sheng-Chu Kuo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . mixture of ¦Â-sitosterol-3-O-¦Â-D-glucoside and stigmasterol-3-O-¦Â-D-glucoside ÏàËÆ¶È:72.5% The Chinese Pharmaceutical Journal 2003 55 109-119 Antiproliferative Constituents from Gynura divaricata subsp. formosana Sheng-Chih Chen*, Li-Ling Hong, Chung-Yang Chang, Chun-Jen Chen, Mei-Hua Hsu, Yuan-Chao Huang, Tai-Hung Huang and Sheng-Chu Kuo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . ¦Â-sitosterol-3-O-¦Â-D-glucoside and stigmasterol-3-O-¦Â-D-glucoside ÏàËÆ¶È:72.5% The Chinese Pharmaceutical Journal 2000 52 261-273 Studies on Anti-inflammatory Constituents of Leucas Mollissima WALL. var. Chinensis Benth ¹Åؑͥ(Chen-Ting Ku), ê?„ÙÖÇ(Sheng-Chih Chen), ÍõÀ^ƽ(Jih-Pyang Wang), …ǽðžI(Jin-Bin Wu), ¹ù„ÙÖú(Sheng-Chu Kuo) Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 24-ethylcholesta-5,22E-dien-3¦Â-O-¦Â-D-pyranoglucosyl-6'-O-palmitate ÏàËÆ¶È:70.7% Phytochemical Analysis 1992 3 38-41 Characterization of acylated steryl glycosides from Euryale ferox by nuclear magnetic resonance spectroscopy Zhao Haoru and Zhao Shoushun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . basilimoside C36H60O6 ÏàËÆ¶È:70% Chemical & Pharmaceutical Bulletin 2007 55(4) 516-519 Two New Triterpenoids and a Steroidal Glycoside from the Aerial Parts of Ocimum basilicum Bina Shaheen SIDDIQUI,Huma ASLAM, Syed Tariq ALI, Sabira BEGUM, and Nasima KHATOON Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . stigmasteryl-3-O-¦Â-D-glucopyranoside and ¦Â-sitosteryl-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:70% Molecules 2009 14 850-867 Bioactive Metabolites from Spilanthes acmella Murr. Supaluk Prachayasittikul, Saowapa Suphapong, Apilak Worachartcheewan, Ratana Lawung, Somsak Ruchirawat and Virapong Prachayasittikul Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . sitgmasterol 3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:70% China Journal of Chinese Materia Medica 2006 31 985-987 Studies on the chemical constituents in herbs of ethanolic extract from gerbs of Dicliptera chinensis GAO Yutao, YANG Xiuwei, AI Tiemin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . stigmasterol-3-O-glucoside ÏàËÆ¶È:70% China Journal of Chinese Materia Medica 1996 21 480-481 HELC Analysts of Mtmic Vinegar processed Yuanhuacine YuanSitong, Zhang Baoxian and Xia Kun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 12-ursen-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:70% Chinese Pharmaceutical Journal 2011 46 341-343 Chemical Constituents of Lysimachia clethroides Duby YUE Shu-mei, CHEN Bai-quan, YUAN Peng-fei, CUI Wei-heng, KANG Wen-yi* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . crotasteroiridocin C39H64O3 ÏàËÆ¶È:70% Zeitschrift f¨¹r Naturforschung B 2006 61 629-635 Behavior of 1,3-Di(tert-butyl)-2,4-bis(tetramethylpiperidino)-1,3,2,4-di-phospha-diboretane towards Boron Halides and Adduct Formation of a Bicyclo[1.1.0]diphosphadiboretane with Tris(pentafluorophenyl)borane K. Knabel, H. Nöth, and R. T. Paine Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . mixture of ¦Â-sitosterol and stigmasterol ÏàËÆ¶È:70% Food Chemistry 2011 127 394-403 Chemical composition and biological activity of Citrus jambhiri Lush Dalia Hamdan, Mahmoud Zaki El-Readi, Ahmad Tahrani, Florian Herrmann, Dorothea Kaufmann, Nawal Farrag, Assem El-Shazly, Michael Wink Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . compound B ÏàËÆ¶È:70% Indian Journal of Chemistry Section B 1996 35B 86-88 Sterol and taraxastane derivatives from Artemisia annua and a rational approach based upon 13C NMR for the identification of skeletal type of amorphane sesquiterpenoids Pawan K Agrawal & Vibha Bishnoi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . stigmasterol-3-O-¦Â-D-glucopyranoside C35H58O6 ÏàËÆ¶È:70% Journal of the Indian Chemical Society 2006 83 513-516 Chemical investigation of the roots of Xanthium strumarium Sankar Kumar Maitra,B.N.Chatterjee,Debi Chakravarti and B.C.Maiti Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . sitosterol-3-O-6-palmityl-¦Â-D-glucopyranoside ÏàËÆ¶È:70% Lishizhen Medicine and Materia Medica Research 2013 24 2859-2860 Study on Chemical Constituents of Alocasia macrorrhiza ZHU Ling-hua, MENG Ling-jie, YE Wen-cai, ZHOU Guang-xiong* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 12-ursen-3-O-¦Â-D-glucopyranoside C36H60O6 ÏàËÆ¶È:70% Chemistry of Natural Compounds 2011 47 91-93 A new carbamic acid from Dryopteris wallichiana Wen-Yi Kang, Chang-Qin Li and Zhi-Qiang Ji Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . stigm asterol-3-O-¦Â-D-glucopyranoside C34H54O7 ÏàËÆ¶È:70% Journal of Chinese Medicinal Materials 2011 34 383-386 Studies on the Diterpenoids of Wedelia prostrata ZHANG Xiang-gang, YAN Wen-qiang, LIN Yan-ting, LIU Xiao-jing, LIN Xiao-yan, ZHANG Yong-hong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . stigmasterol 3-O-¦Â-D-glucopyranoside C35H58O6 ÏàËÆ¶È:70% West China Journal of Pharmaceutical Sciences 2009 24 007-009 Chemical constituents of Paris polyphylla var. pseudothibetica XIAO Cao-mao, HUANG Jing, TAN Xiao-yan, TANG Min, ZHANG Hao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . stigmast-5-en-3¦Â-ol-3-O-¦Â-D-(2'-n-triacontanoyl) glucopyranoside C65H118O7 ÏàËÆ¶È:69.7% Journal of Asian Natural Products Research 2012 14 301-307 New steroidal glycoside ester and aliphatic acid from the fruits of Lycium chinense Woo-Suk Jung,Ill-Min Chung,Mohd Ali and Ateeque Ahmad Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . aglycone-II ÏàËÆ¶È:69.7% Yakugaku Zasshi 1983 103 43-48 The Principles of Tetragonia tetragonoides Having an Antiulcerogenic Activity. I. Isolation and Identification of Sterylglucoside Mixture (Compound A) EMI OKUYAMA, MIKIO YAMAZAKI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . 3-O-¦Â-D-Glucopyranosyl Stigmasterol C35H57O ÏàËÆ¶È:67.5% Chemistry of Natural Compounds 2004 40 137-140 PHYTOCHEMICAL STUDIES OF Berberis vulgaris S. Saied and S. Begum Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . ¦Â-sitosterol 3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:67.5% China Journal of Chinese Materia Medica 2006 31 985-987 Studies on the chemical constituents in herbs of ethanolic extract from gerbs of Dicliptera chinensis GAO Yutao, YANG Xiuwei, AI Tiemin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . ¦Â-sitosterol ÏàËÆ¶È:67.5% China Journal of Chinese Materia Medica 2002 27 752-754 Studies on the Chemical Constituents in Radix Astilbes Chinensis SUN Hongxiang, YE Yiping, YANG Ke Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . gomphsterol ¦Â-D-glucoside C35H56O6 ÏàËÆ¶È:67.5% Natural Product Sciences 2006 12 89-93 Chemical Constituents of Gomphrena globosa. II Dinda, Biswanath; Ghosh, Biplab; Achari, Basudev; Arima, Shiho; Sato, Nariko; Harigaya, Yoshihiro Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 25 . 3-O-(6'-O-palmitoyl)¦Â-D-glucopyranosyl stigmasterol ÏàËÆ¶È:67.5% Phytochemistry 1994 37 1671-1677 Triterpene saponins fromMyrsine pellucida Catherine Lavaud, Georges Massiot, Jose¡äBravo Barrera, Christian Moretti, Louisette Le Men-Olivier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 26 . stigmasterol tritriacontanate C62H112O2 ÏàËÆ¶È:67.5% Chinese Herbal Medicines 2011 3 244-246 A New Stigmasterol Ester from Aeschynomene indica CHEN Jia-yuan, TAN Xiao, LU Wen-jie, YA Qi-kang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 27 . ((2R,3S)-3-Acetoxy-6-((3S,10R,13R,17R)-17-((2R,5S,E)-5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[¦Á]phenanthren-3-yloxy)-3,6-dihydro-2H-pyran-2-yl)methyl acetate ÏàËÆ¶È:67.5% Archives of Pharmacal Research 2012 35 455-460 Novel Human Umbilical Vein Endothelial Cells (HUVEC)-Apoptosis Inhibitory Phytosterol Analogues: Insight into Their Structure-Activity Relationships Sujin Lee,Sony Marharjan,Jong-Wha Jung,Nam-Jung Kim,Kyeojin Kim,Young Taek Han,Changjin Lim,Hyun-Jung Choi,Young-Geun Kwon,and Young-Ger Suh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 28 . stigmasterol-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:67.5% Chinese Traditional and Herbal Drugs 2008 39 972-975 Chemical constituents from roots of Millettia speciosa WANG Chun-hua; WANG Ying; WANG Guo-cai; YA Ji; ZHANG Xiao-qi; YE Wen-cai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 29 . ursolic acid C30H48O3 ÏàËÆ¶È:67.5% Chinese Traditional and Herbal Drugs 1998 29 435-438 Chemical Constituents from Maqianzi (Strychnos nux-vomica) Liu Xikui and Li Wei(Laboratory of Phytochemistry; Kunming Institute of Botany; Chinese Academy of Sciences; Kuming ); Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-10-29 16:47:23













»Ø¸´´ËÂ¥