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ר¼Ò¾Ñé: +726 - PhEPI: 3
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2Â¥2013-10-06 12:13:11
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3Â¥2013-10-06 12:27:54
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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£º¹²²éµ½12767¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¦Â-sitosterol ÏàËÆ¶È:100% 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:100% 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 . campesterol ÏàËÆ¶È:100% 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 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 . ¦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 6 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:96.5% Acta Bot. Boreal. -Occident. Sin. 2004 24 1292-1294 Chemical constituents from Saussurea polycolea LI Yu-lin, WANG Hong-lun, SUO You-rui Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ¦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 8 . ¦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 9 . ¦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 10 . ¦Â-sitosterol ÏàËÆ¶È:96.5% Journal of Asian Natural Products Research 2002 4 73-79 A NEW COMPOUND FROM GASTRODIA ELATA BLUME YONG-QING XIAO, LI LI, XIAO-LIN YOU, BAO-LIN BIAN, XIN-MIAO LIANG and YI-TAO WANG Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . lawsaritol A C29H50O2 ÏàËÆ¶È:96.5% Natural Product Research 1994 4 195-201 Isolation and Characterization of a Dihydroxysterol from Lawsonia inermis Sarita Gupta; Mohammad Ali; M. Sarwar Alam; Masatake Niwa; Tatsuko Sakai Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ¦Â-sitosterol ÏàËÆ¶È:96.5% Natural Product Research 1994 4 195-201 Isolation and Characterization of a Dihydroxysterol from Lawsonia inermis Sarita Gupta; Mohammad Ali; M. Sarwar Alam; Masatake Niwa; Tatsuko Sakai Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ¦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 |

4Â¥2013-10-06 14:39:19
jiyannangxj
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5Â¥2013-10-07 18:00:50
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
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ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ

6Â¥2013-10-07 18:05:35
jiyannangxj
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- É¢½ð: 32
- ºì»¨: 109
- Ìû×Ó: 2948
- ÔÚÏß: 630.8Сʱ
- ³æºÅ: 965914
- ×¢²á: 2010-03-09
- ÐÔ±ð: MM
- רҵ: ÌìÈ»Óлú»¯Ñ§
7Â¥2013-10-07 18:16:06
wangkaibo123
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8Â¥2013-10-07 20:05:46














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