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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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×Ä£Äâͼ
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