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namujila

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[ÇóÖú] ml4 ÒÑÓÐ1È˲ÎÓë

13C NMR (126 MHz, CDCl3) ¦Ä11.86,11.98,18.78,19.03,19.40,19.83,21.08,23.05,24.31,26.03,28.25,29.12,31.67,31.90,31.91,33.93,36.15,36.50,37.25,39.76,42.32,45.82,50.12, 56.04,56.76,71.81,121.73,140.75



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namujila: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-11 09:31:11
1 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:100%
Natural Product Research and Development          2013          25          1367-1369
Study on the Chemical Constituents of Fruticosa potentilla L.
XU Xiao-jie, WANG Wei, WANG Yu-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     ¦Â-Sitosterol
    ÏàËÆ¶È:100%
Zeitschrift f¨¹r Naturforschung C          2012          67          172-180
Anti-Helicobacter pylori Activity of the Methanolic Extract of Geum iranicum and its Main Compounds
Somayeh Shahani, Hamid R. Monsef-Esfahani, Soodabeh Saeidnia, Parastoo Saniee, Farideh Siavoshi, Alireza Foroumadi, Nasrin Samadi, and Ahmad R. Gohari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.5%
Phytochemistry          2004          65          2463-2470
Biosynthesis of the irregular monoterpene artemisia ketone, the sesquiterpene germacrene D and other isoprenoids in Tanacetum vulgare L. (Asteraceae)
Dirk Umlauf, Josef Zapp, Hans Becker, Klaus Peter Adam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     sitosterol
    ÏàËÆ¶È:96.5%
Chemical & Pharmaceutical Bulletin          1979          27          38-42
Carbon-13 Nuclear Magnetic Resonance of 24-Substituted Steroids
NAOYUKI KOIZUMI,YOSHINORI FUJIMOTO,TORU TAKESHITA and NOBUO IKEKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     stigmast-4-en-3¦Â-ol
C29H50O     ÏàËÆ¶È:96.5%
Chemistry of Natural Compounds          2009          45          129-131
CHEMICAL INVESTIGATION AND ANTIBACTERIAL STUDY OF HEXANE EXTRACT OF LEAVES OF Finlaysonia obovata
Pravat Manjari Mishra and A. Sree
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.5%
Chemistry of Natural Compounds          2000          36          595-598
13C NMR SPECTRA OF FUNCTIONALLY SUBSTITUTED 3 ¦Â-CHLORODERIVATIVES OF CHOLESTEROL AND ¦Â -SITOSTEROL
N. V. Kovganko, Zh. N. Kashkan, and E. V. Borisov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:96.5%
Acta Botanica Boreali-Occidentalia Sinica          2004          24          1292-1294
Chemical constituents from Saussurea polycolea
LI Yu-lin, WANG Hong-lun, SUO You-rui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.5%
Acta Botanica Boreali-Occidentalia Sinica          2008          28          1246-1249
Chemical Constituents in the Leaves of Alsophila spinulosa
CHEN Feng-zheng, XIANG Qing-xiang, LI Shu-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.5%
Acta Botanica Sinica          1999          41          107-110
Chemical constituents of the Anemone tomentosa Root
Wang Jun-Ru, Peng Shu-Lin, Wang Ming-Kui, Feng Jun-Tao, Ding Li-Sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.5%
Journal of Chinese Pharmaceutical Sciences          1999          8          237-240
Chemical Constituents of Stelmatocrypton khasianum
Zhang Qingying; Zhao Yuying; Ma Libin; Cheng Tieming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.5%
Journal of Chinese Pharmaceutical Sciences          2005          14          75-78
Chemical Constituents of Hedysarum gmelinii
LIU Yi; MA Xiao-xia; CHEN Hu-biao; TU Guang-zhong; HE Jiu-ming; and ZHAO Yu-ying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.5%
Guihaia          2007          27          140-142
Chemical constituents from leaves of Livistona chinensis
LIU Zhi-Ping; CUI Jian-Guo ; LIU Hong-Xing; HUANG Chu-Sheng; ZHONG Zhen-Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     ¦Â-sitosterol
C33H42O19     ÏàËÆ¶È:96.5%
Natural Product Research          1995          7          35-41
New Cytotoxic Fatty Acid from Desmos cochinchinensis (Annonaceae)
Nan-Jun Sun; David K. Ho; X. Eric Hu; Jeffrey M. Sneddon; Ralph E. Stephens; John M. Cassady
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     stigmast-5-ene-3¦Â-ol
C29H50O     ÏàËÆ¶È:96.5%
Natural Product Research          2006          20          665-670
Potent tyrosinase inhibitors from Trifolium balansae
Temine Şabudak; Mahmut Tareq Hassan Khan; M Iqbal Choudhary; Sevil Oksuz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     ¦Â-sitosterol
    ÏàËÆ¶È:96.5%
Natural Product Research          2006          20          860-865
A new dihydroisocoumarin from the rhizomes of Notopterygium forbesii
Yan-Hui Li; Fan Luo; Shu-Lin Peng; Jian Liang; Li-Sheng Ding
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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