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qqzhao: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-07-04 17:50:48
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qqzhao: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-07-04 17:50:48
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°´´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£º¹²²éµ½666¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . farnesol ÏàËÆ¶È:93.7% Planta Medica 1980 40 288-294 Diterpene Ketols with Antimicrobial Activity from Bifurcaria bifurcata J. F. Biard, J. F. Verbist, Y. Letoumeux, R. Floch Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (2E,6E)-farnesol ÏàËÆ¶È:93.7% Phytochemistry 1996 43 105-109 Biotransformation of acyclic terpenoid (2E,6E)-farnesol by plant pathogenic fungus Glomerella cingulata Mitsuo Miyazawa, Hirokazu Nankai, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ambliofuran C22H32O4 ÏàËÆ¶È:87.5% Journal of Natural Products 1988 Vol 51 1014 Chemistry of Sponges, V. Dictyodendrillolide, a New Prenylated Butenolide from a Sponge R. C. Cambie, Patricia R. Bergquist, P. Karuso Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . trans-farnesol ÏàËÆ¶È:87.5% Phytochemistry 1986 25 871-876 Acyclic sesquiterpene oligoglycosides from pericarps of Sapindus mukurossi Ryoji Kasai, Hiroko Fujino, Tatsuro Kuzuki, Wu-Hsiung Wong, Chie Goto, Noboru Yata, Osamu Tanaka, Fujiko Yasuhara, Shozo Yamaguchi Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . all-E-geranylgeraniol C20H34O ÏàËÆ¶È:83.3% Phytochemistry 1989 28 3159-3162 Terpenoids and an apocarotenoid from seeds of Bixa orellana Isaac J.O. Jondiko,Gerald Pattenden Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Squalene ÏàËÆ¶È:81.2% Guihaia 2006 26 687-689 Extraction and structure identification of Siraitia grosvenorii squalene CHEN Quan-bin; CHENG Zhong-quan; YANG Jian-xiang; YI Xiang-hui; DONG Chao-min Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . squalene ÏàËÆ¶È:81.2% China Journal of Chinese Materia Medica 2006 31 1168-1171 Compounds from marine mangrove plant Bruguiera sexangula var. rhynchopetala BAO Shuyun, LIN Wenhan Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . thorectolide monoacetate ÏàËÆ¶È:81.2% Journal of Natural Products 1988 Vol 51 1014 Chemistry of Sponges, V. Dictyodendrillolide, a New Prenylated Butenolide from a Sponge R. C. Cambie, Patricia R. Bergquist, P. Karuso Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . squalene ÏàËÆ¶È:81.2% Acta Pharmaceutica Sinica 2005 Vol 40 935-939 Chemical constituents from the mangrove plant Ceriops tagal ZHANG Yan; DENG Zhi-wei; GAO Tian-xiang; FU Hong-zheng; LIN Wen-han Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . trans-farnesol ÏàËÆ¶È:81.2% Phytochemistry 1986 25 871-876 Acyclic sesquiterpene oligoglycosides from pericarps of Sapindus mukurossi Ryoji Kasai, Hiroko Fujino, Tatsuro Kuzuki, Wu-Hsiung Wong, Chie Goto, Noboru Yata, Osamu Tanaka, Fujiko Yasuhara, Shozo Yamaguchi Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . squalene ÏàËÆ¶È:81.2% Chinese Traditional and Herbal Drugs 2010 41 1056-1060 Chemical constituents from Kalimeris indica XU Wen-qing; GONG Xiao-jian; ZHOU Xin; MEI Xiao-ping; CHEN Bo-bing Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Squalene ÏàËÆ¶È:81.2% Journal of the Chinese Chemical Society 2000 47 1131-1136 The Low Polar Constituents from Bidens Pilosa L. var. minor (Blume) Sherff Ming-Huey Chang, Guei-Jane Wang,Yueh-Hsiung Kuo and Ching-Kuo Lee* Structure 13C NMR ̼Æ×Ä£Äâͼ |

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