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2Â¥2013-09-14 17:53:51
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3Â¥2013-09-14 19:14:56
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- É¢½ð: 104
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4Â¥2013-09-14 19:15:55
wangkaibo123
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ר¼Ò¾Ñé: +726 - PhEPI: 3
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mrdone.0907: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ×î½ü±È½Ï棬»Ø¸´µÄÓÐЩ³Ù 2013-09-17 15:44:26
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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£º¹²²éµ½2189¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . cycloprotobuxinamine C29H46N2O5 ÏàËÆ¶È:65.5% Acta Botanica Sinica 1996 38 483-488 Two New Buxus Alkaloids from Buxus microphylla Sieb. Et Zucc Du Jiang, QiuMing-hua and Nie Rui-lin L¨¹Yang, Wu Nan and Zheng Qi-tai Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . neomyrrhaol C30H52O4 ÏàËÆ¶È:63.3% Planta Medica 2009 75 351-355 Isolation and Biological Activities of Neomyrrhaol and Other Terpenes from the Resin of Commiphora myrrha Shu-Lan Su,Jin-Ao Duan,Yu-Ping Tang, Xu Zhang1, Li Yu, Feng-Rong Jiang,Wei Zhou1, Dan Luo,An-Wei Ding Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¦Â,22¦Á-dihydroxy-lanosta-8,24E-diene-25-peroxide C30H50O4 ÏàËÆ¶È:63.3% Chinese Chemical Letters 2000 11 45-48 Triterpenoids from Fuscoporia obliqua Jian HE, Xiao zhang FENG, Bin ZHAO, Yang LU Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . fuscoporianol B C30H50O4 ÏàËÆ¶È:63.3% Journal of Asian Natural Products Research 2001 3 55-61 Three New Triterpenoids from Fuscoporia Obliqua JJAN HE, XIAO-ZHANG FENG, YANG LU and BIN ZHAO Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ¦Â-kudinlactone C30H46O5 ÏàËÆ¶È:63.3% Phytochemistry 1996 43 443-445 Triterpenoid glycosides from Ilex kudincha Ming-An Ouyang, Han-Qing Wang, Zi-Li Chen, Chong-Ren Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ¦Â-Kudinlactone C30H46O5 ÏàËÆ¶È:63.3% Phytochemistry 1996 41 871-877 Triterpenes and triterpenoid glycosides from the leaves of Ilex kudincha Ming-An Ouyang, Chong-Ren Yang, Zi-Li Chen, Han-Qing Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 12 ÏàËÆ¶È:63.3% Phytochemistry 1992 31 4263-4274 Cycloartanes and other terpenoids and phenylpropanoids from Monocyclanthus vignei Hans Achenbach, Dieter Frey Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 17,24-epoxy-25-hydroxy-3-oxobaccharan-21-oic acid C30H48O5 ÏàËÆ¶È:63.3% The Journal of Organic Chemistry 2004 69 3350-3358 Silvestrol and Episilvestrol, Potential Anticancer Rocaglate Derivatives from Aglaia silvestris Bang Yeon Hwang, Bao-Ning Su, Heebyung Chai, Qiuwen Mi, Leonardus B. S. Kardono, Johar J. Afriastini, Soedarsono Riswan, Bernard D. Santarsiero, Andrew D. Mesecar, Robert Wild, Craig R. Fairchild, Gregory D. Vite, William C. Rose, Norman R. Farnsworth, Ge Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . colossolactone C C32H46O6 ÏàËÆ¶È:62.5% Journal of Natural Products 2001 64 236-239 Colossolactones, New Triterpenoid Metabolites from a Vietnamese Mushroom Ganoderma colossum Peter Kleinwächter, Ngo Anh,Trinh Tam Kiet,Brigitte Schlegel, Hans-Martin Dahse, Albert Härtl, and Udo Gräfe Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2¦Á,3¦Â,19¦Á-Trihydroxy-28-norurs-12-ene C29H48O3 ÏàËÆ¶È:62.0% Chemical & Pharmaceutical Bulletin 2005 53(10) 1338-1341 Sesquiterpenes, Nortriterpenes and Other Constituents from Ligularia tongolensis Yi Feng HAN,Jing PAN,Kun GAO,and Zhong Jian JIA Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 20(¦Á),24(S)-epoxy-3¦Â,6¦Á,25-trihydroxycycloartan-16-one C30H48O5 ÏàËÆ¶È:62.0% Journal of Natural Products 2001 64 1179-1182 Secondary Metabolites from the Roots of Astragalus zahlbruckneri Ihsan Çalis,Hasan Abou Gazar, Sonia Piacente, and Cosimo Pizza Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 5 C27H44O2 ÏàËÆ¶È:62.0% Tetrahedron Letters 2002 43 1151-1155 Deoxygenation of aliphatic acetate derivatives using electrogenerated organic amalgams Lizeth M. Fragoso-Luna, Bernardo A. Frontana-Uribe, Jorge C¨¢rdenas Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . halistanol sulfate C29H52O12S3Na3 ÏàËÆ¶È:62.0% Tetrahedron letters 1981 22 1985-1988 Bioactive marine metabolites II. Halistanol sulfate, an antimicrobial novel steroid sulfate from the marine sponge halichondria cf. moorei bergquist N. Fusetani, S. Matsunaga, S. Konosu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 2¦Á,3¦Â,19¦Á-trihydroxy-28-norurs-12-ene C29H48O3 ÏàËÆ¶È:62.0% Chemistry Letters 2005 34 892-893 Two New Nortriterpenes from Ligularia tongolensis Yi Feng Han, Kun Gao and Zhong Jian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . Buxruguline D C29H48N2O3 ÏàËÆ¶È:62.0% Natural Products and Bioprospecting 2011 1 71-74 Triterpenoid alkaloid derivatives from Buxus rugulosa Yu-Xin Yan, Lin Zhou, Yun Sun, Jian-Chao Chen, Jia Su, Yan Li, Ming-Hua Qiu Structure 13C NMR ̼Æ×Ä£Äâͼ |

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