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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£º¹²²éµ½457¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 12a ÏàËÆ¶È:65% Phytochemistry 1989 28 2717-2721 Sesquiterpenoids and phenolics of Pulicaria paludosa Arturo San Feliciano,Manuel Medarde,Marina Gordaliza,Esther Del Olmo,Jos¨¦ M. Miguel del Corral Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Â-1,15-dihydro-8,10-diepi-chandonanthone C20H32O4 ÏàËÆ¶È:65% Tetrahedron 2009 65 4035-4043 Terpenoids from the liverwort Chandonanthus hirtellus Yanmei Wang, Leslie J. Harrison, Benito C. Tan Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . senecrassidiol-9-O-¦Â-D-glucopyranoside C21H36O7 ÏàËÆ¶È:61.9% Acta Botanica Sinica 2004 45 1002-1008 Terpenoids and Phenols from Taiwania flousiana XIANG Ying, YANG Sheng-Ping, ZHAN Zha-Jun, YUE Jian-Min Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 1¦Â-O-¦Â-D-glucopyranosyl-5¦Á,6¦ÁH-eudesma-3-en-12,6¦Á-olide C21H32O8 ÏàËÆ¶È:61.9% Planta Medica 2005 71 543-547 New Sesquiterpenes from Sonchus transcaspicus Han, Yi-Feng; Zhang, Qi; Gao, Kun; Jia, Zhong-Jian Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 1¦Â-O-¦Â-D-glucopyranosy-5¦Á,6¦ÂH-eudesma-3-en-12,6¦Á-olide C21H32O8 ÏàËÆ¶È:61.9% Chinese Chemical Letters 2005 16 491-493 Two New Eudesmanoildes from Sonchus transcaspicus Yi Feng HAN, Xin LI, Kun GAO, Zhong Jian JIA Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Boarioside C21H38O8 ÏàËÆ¶È:61.9% Phytochemistry 1995 40 853-855 Boarioside, a eudesmane glucoside from Maytenus boaria O. Muñoz, C. Galeffi, E. Federici, J. A. Garbarino, M. Piovano, M. Nicoletti Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . amaloside A ÏàËÆ¶È:61.9% Phytochemistry 1993 33 687-689 Steroids from Amalocalyx yunnanensis Shen Xiao-Ling, Hu Ying-Jie, An Yin-Ling, Zhang Mu Quan Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . oplodiol 1-O-¦Â-D-glucopyranoside ÏàËÆ¶È:61.9% Chemical & Pharmaceutical Bulletin 2012 60 306-314 Sesquiterpenes and Other Constituents from Dendranthema zawadskii var. latilobum Hyun Jung Shin, So Young Lee, Ju Sun Kim, Sanghyun Lee, Ran Joo Choi, Ha Sook Chung, Yeong Shik Kim and Sam Sik Kang Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . alatoside E C19H34O7 ÏàËÆ¶È:60% Phytochemistry 2003 63 835-839 Eudesmane and megastigmane glucosides from Laggera alata Qunxiong Zheng, Zhaojun Xu, Xianfeng Sun, Wei Yao, Handong Sun,Christopher H. K. Cheng, Yu Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . sammangaoside A ÏàËÆ¶È:60% Acta Pharmaceutica Sinica 2008 Vol 43 173-180 Chemical constituents from the leaves of Broussonetia papyrifera FENG Wei-sheng; LI Hong-wei; ZHENG Xiao-ke; KUANG Hai-xue; CHEN Sui-qing; WANG Yan-zhi; ZANG Xin-yu Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . dendranthemoside B ÏàËÆ¶È:60% Natural Product Sciences 2009 15 90-95 Phytochemical Constituents of Nelumbo nucifera Kim, Ki-Hyun; Chang, Sang-Wook; Ryu, Shi-Yong; Choi, Sang-Un; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . longipin-2-ene-1¦Â,7¦Â,9¦Á-15-tetrahydroxy 7,15-acetonide acetate ÏàËÆ¶È:60% Phytochemistry 1993 32 1219-1223 Longipinene derivatives from Stevia origanoides Carlos M. Cerda-Garc¨ªa-Rojas, Eugenio S¨¢nchez-Arreola, Pedro Joseph-Nathan, Luisa U. Rom¨¢n, Juan D. Hernandez Structure 13C NMR ̼Æ×Ä£Äâͼ |

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