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1 . daucosterol linoleate ÏàËÆ¶È:69.0% Chinese Pharmaceutical Journal 2007 42 661-663 Studies on Chemical Constituents of Paeonia veitchii L. WANG Rui, CHOU Gui-xin, ZHU En-yuan, WANG Zheng-tao, BI Kai-shun Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . skimmiarepin C ÏàËÆ¶È:67.8% Natural Product Research 2004 18 117-122 A new insecticidal protolimonoid from Aegle Marmelos J.K.R. Radhika Samarasekera; Bhupinder P. S. Khambay; K. Patrick Hemalal Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Citruslanosteroside C56H100O7 ÏàËÆ¶È:67.8% Natural Product Research 2010 24 610-620 Phytochemical investigation of the fruit peels of Citrus reticulata Blanco M. Aasim Khan; M. Ali; Prawez Alam Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ligustrin B ÏàËÆ¶È:67.2% Phytochemistry 1997 46 977-979 Acylated triterpenoids from Ligustrum ovalifolium Koichi Machida, Toshio Yamaguchi, Yoshiko Kamiya, Masao Kikuchi Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 12,6'-dioctanoyl ginsenoside Rh2 (D-Rh2) ÏàËÆ¶È:67.2% Bioorganic & Medicinal Chemistry Letters 2012 22 1082-1085 Structural modification of ginsenoside Rh2 by fatty acid esterification and its detoxification property in antitumor Gong-Qing Wei, Yi-Nan Zheng, Wei Li, Wen-Cong Liu, Ting Lin, Wei-Yun Zhang, Hai-Feng Chen,Jin-Zhang Zeng, Xiao-Kun Zhang, Quan-Cheng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . daucosterol-6'-linoleate ÏàËÆ¶È:67.2% Journal of Shenyang Pharmaceutical University 2008 25 883-885 Chemical constituents from the seeds of Castanea mollissima Blume(III) LONG Zhi-min, WU Li-jun, JIANG Bing-ya, SUN Bo-hang, HUANG Jian, GAO Hui-yuan Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Ginsenoside PM1 ÏàËÆ¶È:65.4% Molecules 2007 12 2140-2150 Isolation, Synthesis and Structures of Cytotoxic Ginsenoside Derivatives Jun Lei, Xiang Li, Xiao-jie Gong and Yi-nan Zheng Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Ginsenoside SM1 ÏàËÆ¶È:65.4% Molecules 2007 12 2140-2150 Isolation, Synthesis and Structures of Cytotoxic Ginsenoside Derivatives Jun Lei, Xiang Li, Xiao-jie Gong and Yi-nan Zheng Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Citrusteryl arachidate C55H98O7 ÏàËÆ¶È:65.4% Natural Product Research 2010 24 610-620 Phytochemical investigation of the fruit peels of Citrus reticulata Blanco M. Aasim Khan; M. Ali; Prawez Alam Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 7¦Â-tert-Butyldimethylsilyloxysitosteryl-9,10-ditert-butyldimethylsilyloxystearate C65H126O5Si3 ÏàËÆ¶È:64.4% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 5¦Á-stigmast-9(11)-en-3¦Â-ol-tetraco santrienoic acid ester ÏàËÆ¶È:63.6% China Journal of Chinese Materia Medica 1996 21 666-667 Studies on Chemical Components of Cynomorium songaricum Rupr. Xu Xiuzhi, Zhang Chengzhong and Li Chong Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . skimmiarepin A ÏàËÆ¶È:63.6% Phytochemistry 1994 36 1303-1306 Protolimonoid and lignans from Zanthoxylum petiolare Mara S.P. Arruda, João B. Fernandes, Paulo C. Vieira, M. Fatima Das G.F. Da Silva, Jose R. Pirani Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 3-O-Carboxymaleinate of ¦Á,¦Â-amyrin ÏàËÆ¶È:63.6% Bioorganic & Medicinal Chemistry 2011 19 1268-1276 Amyrin esters induce cell death by apoptosis in HL-60 leukemia cells Francisco W. A. Barros, Paulo N. Bandeira, Daisy J. B. Lima, Assuero S. Meira, Silvana S. de Farias,Maria Rose J. R. Albuquerque, H¨¦lcio S. dos Santos, Telma L. G. Lemos, Manoel Odorico de Morais,Let¨ªcia Veras Costa-Lotufo, Claudia do ¨® Pessoa Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . shishicrellastatin A C56H83Na3O16S3 ÏàËÆ¶È:63.6% Bioorganic & Medicinal Chemistry 2011 19 6594-6598 Shishicrellastatins, inhibitors of cathepsin B, from the marine sponge Crella (Yvesia) spinulata Shuhei Murayama, Yasufumi Imae, Kentaro Takada, Jo Kikuchi, Yoichi Nakao, Rob W.M. van Soest, Shigeru Okada, Shigeki Matsunaga Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . balanoinvolin ÏàËÆ¶È:63.6% Journal of Anhui Agricultural Sciences 2012 40 9641-9643 Study on the Chemical Constituents of Mirabilis himalaica Roots YANG Pan-pan et al Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ¦Â-sitosterol-3-O-(6'-linolenoyl)-¦Â-D-glucopyranoside ÏàËÆ¶È:63.6% Indian Journal of Chemistry Section B 1997 36B 1038-1043 Triterpenoids and other compounds from Euphorbia esula and E.petiolata Yan-Ping Shi & Zhong-Jian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (+/-)-3¦Á,7¦Á,12¦Á-Tris(3-{[2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6-yl]oxycarbonyl}propanoyloxy)-5¦Â-cholan-24-oic aci C123H196O17 ÏàËÆ¶È:63.3% Steroids 2013 78 435-453 New propanoyloxy derivatives of 5¦Â-cholan-24-oic acid as drug absorption modifiers Lenka Coufalov¨¢, Lech Mr¨®zek, Lucie R¨¢rov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Katar¨ªna Kr¨¢l¡¯ov¨¢, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . ligustrin A ÏàËÆ¶È:63.1% Phytochemistry 1997 46 977-979 Acylated triterpenoids from Ligustrum ovalifolium Koichi Machida, Toshio Yamaguchi, Yoshiko Kamiya, Masao Kikuchi Structure 13C NMR ̼Æ×Ä£Äâͼ |

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