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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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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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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