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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£º¹²²éµ½112¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . tetrecentronside B C26H32O11 ÏàËÆ¶È:66.6% Phytochemistry 2000 53 1001-1003 Two glycosides from the stem bark of Tetracentron sinense Jin-hai Yi, Guo-lin Zhang, Bo-gang Li, Yao-zu Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 2-¼×Ñõ»ù-4-ÒÒÏ©±½»ù-¦Â-D-ßÁà«ÆÏÌÑÌÇÜÕ C15H20O7 ÏàËÆ¶È:64.7% Journal of Tropical and Subtropical Botany 2012 20 585-590 Metabolits of Fusarium solani ZHANG Mei, XU Liang-xiong, XUE Jing-hua, WEI Xiao-yi Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . grevilloside D C16H24O8 ÏàËÆ¶È:58.8% Phytochemistry 2008 69 2749-2752 Grevillosides A¨CF: Glucosides of 5-alkylresorcinol derivatives from leaves of Grevillea robusta Yukiko Yamashita, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . coniferin ÏàËÆ¶È:58.8% Planta Medica 1982 46 145-148 Phenolic Glycosides of Paulownia tomentosa Bark O. Sticher and M. F. Lahioub Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . rhodiocyanoside B C5H7NO ÏàËÆ¶È:58.8% Chemical & Pharmaceutical Bulletin 1996 44 2086-2091 Bioactive Constituents of Chinese Natural Medicines. II. Rhodiolae Radix. (1). Chemical Structures and Antiallergic Activity of Rhodiocyanosides A and B from the Underground Part of Rhodiola guadrifida (PALL.) FISCH. et MEY. (Crassulaceae) Masayuki YOSHIKAWA,Hiromi SHIMADA,Hiroshi SHIMODA,Nobutoshi MURAKAMI,Johji YAMAHARA and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . coniferin ÏàËÆ¶È:58.8% Chemistry of Natural Compounds 2009 45 371-373 BALANOINVOLIN, A NEW STEROID DERIVATIVEFROM Balanophora involucrate Bing Luo, Kun Zou, Zhiyong Guo, Feijun Dan, Juizhi Wang, and Hui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . methylconiferin ÏàËÆ¶È:58.8% Chemistry of Natural Compounds 2009 45 371-374 BALANOINVOLIN, A NEW STEROID DERIVATIVEFROM Balanophora involucrate Bing Luo, Kun Zou, Zhiyong Guo, Feijun Dan, Juizhi Wang, and Hui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (+)-pinoresinol-4,4'-O-bisglucopyranoside ÏàËÆ¶È:58.8% China Journal of Chinese Materia Medica 2007 32 1303-1305 Studies on lignin glycosides in root from Ilex pubescens YANG Xin, DING Yi, ZHANG Dongming Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . junipetrioloside B C16H23O10 ÏàËÆ¶È:58.8% Phytochemistry 1997 45 1679-1682 Phenylpropanoids from leaves of Juniperus phoenicea Gilles Comte, Joseph Vercauteren, Albert J. Chulia, Daovy P. Allais, Christiane Delage Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Vanilloloside C11H16O9 ÏàËÆ¶È:58.8% Phytochemistry 1994 35 209-215 Phenolic constituents of phellodendron amurense bark Yoshiteru Ida, Yohko Satoh, Masumi Ohtsuka, Miki Nagasao, Junzo Shoji Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . coniferin ÏàËÆ¶È:58.8% Phytochemistry 1993 33 1215-1219 Lignan and phenylpropanoid glycosides from Osmanthus asiaticus Masataka Sugiyama, Eiko Nagayama, Masao Kikuchi Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Coniferin ÏàËÆ¶È:58.8% Korean Journal of Pharmacognosy 2009 40(4) 326-333 Phytochemical Studies on Lonicera Caulis (2) - Aliphatic and Phenolic Compounds Kim, Ju-Sun; Yean, Min-Hye; Seo, Hyun-Kyu; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Coniferin ÏàËÆ¶È:58.8% Planta Medica 1982 46 145-148 Phenolic Glycosides of Paulownia tomentosa Bark 0. Sticher and M. F. Lahioub Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . coniferin ÏàËÆ¶È:58.8% Phytochemistry 1987 26 322-323 Coniferin¡ªan astringent glycoside in citrus James H. Tatum,Robert E. Berry Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-08-03 20:55:26
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