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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£º¹²²éµ½3402¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 21¦Â,25-dimethylmelianodiol C32H52O5 ÏàËÆ¶È:78.1% Journal of Natural Products 2002 65 562-565 Triterpenoid Constituents of Raulinoa echinata Maique W. Biavatti, Paulo C. Vieira, M. F¨¢tima G. F. da Silva, Joao B. Fernandes, and S¨¦rgio Albuquerque Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 21¦Á,25-dimethylmelianodiol C32H52O5 ÏàËÆ¶È:75% Journal of Natural Products 2002 65 562-565 Triterpenoid Constituents of Raulinoa echinata Maique W. Biavatti, Paulo C. Vieira, M. F¨¢tima G. F. da Silva, Joao B. Fernandes, and S¨¦rgio Albuquerque Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 21¦Á-methyl-25-ethylmelianodiol C33H54O5 ÏàËÆ¶È:72.7% Chemical & Pharmaceutical Bulletin 2011 59(8) 1003-1007 Limonoids and Triterpenoids from the Seeds of Melia azedarach Hong-Bing LIU, Chuan-Rui ZHANG, Shi-Hui DONG, Lei DONG, Yan WU, and Jian-Min YUE Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 2¦Á,25-dimethylmeli-anodiol-[(21R,23R)-epoxy-24-hydroxyl-21¦Á,25-methoxy] tirucalla-7-en-3-one ÏàËÆ¶È:71.8% Chinese Journal of Natural Medicines 2009 7 31-33 Triterpenes from the Fruits of Phellodendron chinense Schneid var. glabriusculum Schneid YAN Chen; WANG Ye; HAO Xiao-Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 21¦Á,25-dimethylmelianodiol C32H52O5 ÏàËÆ¶È:71.8% Chinese Journal of Natural Medicines 2010 8 97-100 Chemical Constituents from the Fruits of Poncirus trifoliata YU Ping; LIANG Jing-Yu; LIU Xin Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 3¦Â-hydroxybauer-7-en-28-oic acid C30H48O3 ÏàËÆ¶È:67.7% Journal of Natural Products 2004 67 2124-2126 Triterpenes from Maesopsis eminii Patrice Aim Fokou, Hans-Georg Stammler, Beate Neumann, Thomas Huber, David Lontsi, Hilaire V. Kemami Wangun, and Norbert Sewald Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 1c ÏàËÆ¶È:67.7% Journal of Natural Products 2007 70 1532-1535 Agladupols A¨CE, Triterpenoids from Aglaia duperreana Bo-Jun Xie, Sheng-Ping Yang, Hua-Dong Chen, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . agladupol E C31H52O5 ÏàËÆ¶È:67.7% Journal of Natural Products 2007 70 1532-1535 Agladupols A¨CE, Triterpenoids from Aglaia duperreana Bo-Jun Xie, Sheng-Ping Yang, Hua-Dong Chen, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 4 ÏàËÆ¶È:67.7% Chemical & Pharmaceutical Bulletin 1996 44 847-849 Isolation of Inhibitors of TPA-Induced Mouse Ear Edema from Hoelen, Poria cocos Haruo NUKAYA,Hirokazu YAMASHIRO,Hirotatsu FUKAZAWA,Hitoshi ISHIDA and Kuniro TSUJI Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . polytolypin C30H46O7 ÏàËÆ¶È:67.7% Journal of Natural Products 1995 Vol 58 1984-1986 Polytolypin, a New Antifungal Triterpenoid from the Coprophilous Fungus Polytolypa hystricis William R. Gamble, James B. Gloer, James A. Scott, David Malloch Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3-oxotirucalla-7,9(11),24-trien-21-oic acid C30H44O3 ÏàËÆ¶È:67.7% Journal of Asian Natural Products Research 2011 13 193-197 Two new triterpenoids from the resin of Boswellia carterii Feng Wang; Zhan-Lin Li; Hong-Hua Cui; Hui-Ming Hua; Yong-Kui Jing; Sheng-Wang Liang Structure 13C NMR ̼Æ×Ä£Äâͼ |

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