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13C-NMR ë®´úÂÈ·Â 500M 12.0, 12.1, 18.9, 19.2, 19.5, 20.0, 21.2, 23.2, 24.5, 26.2, 28.4, 29.3, 31.8, 32.1, 34.1, 36.3, 36.7, 37.4, 39.9, 42.5, 42.5, 46.0, 50.3, 56.2, 56.9, 71.9, 140.9 |
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½14161¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¦Â-sitosterol ÏàËÆ¶È:96.4% Zeitschrift f¨¹r Naturforschung C 2003 58 441-445 Feeding Stimulative Activity of Steroidal and Secoiridoid Glucosides and Their Hydrolysed Derivatives toward the Olive Weevil (Dyscerus perforatus) E. Kadowaki, Y. Yoshida, N. Baba, and S. Nakajima Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:96.4% Molecules 2013 18 1325-1336 Chemical Constituents of Caesalpinia decapetala (Roth) Alston Xiao-Hua Wei, Sheng-Jie Yang, Na Liang, De-Yu Hu, Lin-Hong Jin, Wei Xue and Song Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ¦Â-sitosterol ÏàËÆ¶È:96.4% Chemistry and Industry of Forest Products 2013 33 133-136 Chemical Constituents from the Branch of Litsea cubeba ( Lour. ) Pers. CHEN Zhan-juan, BI He-ping, FAN Chao-jun, BAO Chang-yu Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . campesterol ÏàËÆ¶È:96.4% Chinese Pharmaceutical Journal 2012 47 500-503 Study on Chemical Constituents of Rosa chinensis Jacq. Flower WANG Xiao-yan; WANG Wen-wen; ZHOU Yong-hui; JIANG Xin-ke; JING Lin-lin; JIA Lu Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ¦Â-sitosterol ÏàËÆ¶È:96.4% Korean Journal of Pharmacognosy 2013 44 1-5 Isolation of Compounds having Inhibitory Activity toward Tyrosinase from Receptaculum Nelumbinis Hyun Woo Cho, Won Seok Jung, Byeong Gwan An, Jung Hee Cho and Su Young Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:96.2% Chemical & Pharmaceutical Bulletin 1993 41 2007-2009 Constituents of Prunus zippeliana Leaves and Branches Junichi KITAJIMA and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:96.2% 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 8 . ¦Â-sitosterol ÏàËÆ¶È:96.2% Korean Journal of Pharmacognosy 2005 36(2) 145-150 Phytochemical Constituents of Cirsium nipponicum (MAX.) Makino Lee, Jong-Hwa; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ |

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