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1 . 2¦Á,3¦Â,19¦Á-Trihydroxy-28-norurs-12-ene C29H48O3 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 2005 53(10) 1338-1341 Sesquiterpenes, Nortriterpenes and Other Constituents from Ligularia tongolensis Yi Feng HAN,Jing PAN,Kun GAO,and Zhong Jian JIA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3,23-disulfate ester of 23-hydroxytormentic acid C30H48O12S2 ÏàËÆ¶È:66.6% Journal of Natural Products 2007 70 1889-1894 Triterpene, Antioxidant, and Antimicrobial Compounds from Melissa officinalis Teresa Mencherini,Patrizia Picerno, Carla Scesa, and Rita Aquino Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-O-¦Á-L-arabinopyranosyl pomolic acid ÏàËÆ¶È:66.6% Phytochemistry 1992 31 3909-3914 Triterpenoids from plants of the sanguisorbeae Gesa Reher, Miloš Bud¨§š¨ªnský Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 2¦Á,3¦Â,19¦Á-trihydroxy-28-norurs-12-ene C29H48O3 ÏàËÆ¶È:66.6% Chemistry Letters 2005 34 892-893 Two New Nortriterpenes from Ligularia tongolensis Yi Feng Han, Kun Gao and Zhong Jian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ¨¢cido torm¨ºntico ÏàËÆ¶È:63.6% Qu¨ªmica Nova 2008 31 744-750 Chemical constituents and antiedematogenic activity of Peltodon radicans (Lamiaceae) Costa, Habdel Nasser Rocha da; Santos, Maria Cristina dos; Alcântara, Antônio Flavio de Carvalho; Silva, Marilda Conceição; França, Roberta Cabral; Pil¨®-Veloso, Dorila Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 2¦Á,3¦Á,19¦Á-Trihydroxy-28-norurs-12-ene C29H48O3 ÏàËÆ¶È:60.6% Chemical & Pharmaceutical Bulletin 2005 53(10) 1338-1341 Sesquiterpenes, Nortriterpenes and Other Constituents from Ligularia tongolensis Yi Feng HAN,Jing PAN,Kun GAO,and Zhong Jian JIA Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 2¦Á,3¦Â,19¦Á,23¦Â-tetrahydroxyurs-12-en-28-oic acid ÏàËÆ¶È:60.6% China Journal of Chinese Materia Medica 2009 34 3047-3050 Triterpenoid constituents in fruits of Psidum guajava SHU Jicheng, CHOU Guixin, WANG Zhengtao Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . euscaphic acid C30H48O5 ÏàËÆ¶È:60.6% China Journal of Chinese Materia Medica 2006 31 1875-1879 Triterpenes from herb of Potentilla chinesis LIU Pu, DUAN Hongquan, PAN Qin, ZHANG Yanwen, YAO Zhi Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 2¦Â,3¦Â,19¦Á-trihydroxyurs-12-en-28-oic acid C30H48O5 ÏàËÆ¶È:60.6% China Journal of Chinese Materia Medica 2006 31 1875-1879 Triterpenes from herb of Potentilla chinesis LIU Pu, DUAN Hongquan, PAN Qin, ZHANG Yanwen, YAO Zhi Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . tormentic acid ÏàËÆ¶È:60.6% Phytochemistry 1992 31 3909-3914 Triterpenoids from plants of the sanguisorbeae Gesa Reher, Miloš Bud¨§š¨ªnský Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3¦Â,6¦Â,19¦Á-Trihydroxy-urs-12-en-28-oic acid-24-carboxylic acid methyl ester C31H48O7 ÏàËÆ¶È:60.6% Molecules 2012 17 504-510 A New Triterpene from the Plant of Uncaria Macroph Guangli Sun, Xiaopo Zhang, Xudong Xu, Junshan Yang, Mingliang Zhong and Jingquan Yuan Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . panaxadione C30H48O5 ÏàËÆ¶È:60.6% Chemical & Pharmaceutical Bulletin 2009 57 283-287 Chemical Constituents from Seeds of Panax ginseng: Structure of New Dammarane-Type Triterpene Ketone, Panaxadione, and HPLC Comparisons of Seeds and Flesh Sachiko Sugimoto, Seikou Nakamura, Hisashi Matsuda, Niichiro Kitagawa and Masayuki Yoshikawa Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . fupenzic acid C30H44O5 ÏàËÆ¶È:60.6% Phytochemistry 1988 27 3975-3976 A triterpene from the fruits of Rubus chingii Masao Hattori,kue-Ping Kuo,Yue-Zhong Shu,Yasuhiro Tezuka,Tohru Kikuchi,Tsuneo Namba Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 3 ÏàËÆ¶È:60.6% Phytochemistry 1988 27 3975-3976 A triterpene from the fruits of Rubus chingii Masao Hattori,kue-Ping Kuo,Yue-Zhong Shu,Yasuhiro Tezuka,Tohru Kikuchi,Tsuneo Namba Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . euscaphic acid ÏàËÆ¶È:60.6% Chinese Traditional and Herbal Drugs 2007 38 1311-1313 ÉßÝ®ÖоßÓп¹°©»îÐÔµÄÈýÝÆÀà³É·Ö ÎâÅàéª;¶ÎºêȪ;Ò¦ÖÇ;ÅËÇÚ;ÕŸ»âÙ Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 2¦Á,3¦Á,19¦Á-trihydroxy-28-norurs-12-ene C29H47O2 ÏàËÆ¶È:60.6% Chemistry Letters 2005 34 892-893 Two New Nortriterpenes from Ligularia tongolensis Yi Feng Han, Kun Gao and Zhong Jian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 3,23-disulfate ester of rotundic acid C30H48O11S2 ÏàËÆ¶È:57.5% Journal of Natural Products 2007 70 1889-1894 Triterpene, Antioxidant, and Antimicrobial Compounds from Melissa officinalis Teresa Mencherini,Patrizia Picerno, Carla Scesa, and Rita Aquino Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . camaldulensic acid C31H50O5 ÏàËÆ¶È:57.5% Journal of Natural Products 1997 60 20-23 Triterpenoids from the Leaves of Eucalyptus camaldulensis var. obtusa Sabira Begum, Farhat, and Bina S. Siddiqui Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 2-epi-tormentic acid C30H48O5 ÏàËÆ¶È:57.5% Phytochemistry 2009 70 1239-1245 Hydroperoxy-cycloartane triterpenoids from the leaves of Markhamia lutea,a plant ingested by wild chimpanzees Damien Lacroix, Soizic Prado, Alexandre Deville, Sabrina Krief, Vincent Dumontet, John Kasenene, Elisabeth Mouray, Christian Bories, Bernard Bodo Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 3¦Â,6¦Â,19¦Á,-23-tetrahydroxy-urs-12-ene C30H50O4 ÏàËÆ¶È:57.5% Natural Product Research 2001 15 177-185 Triterpenes from Mimusops elengi Nusrat Jahan; Abdul Malik; Ghulam Mustafa; Zaheer Ahmad; Saeed Ahmad; Erum Anis; Shahid Malik; Shahida Shujaat; Night Afza; Atta-ur-rahman Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 3¦Â,19¦Á,23¦Â-trihydroxylurs-12-en-28-oic acid ÏàËÆ¶È:57.5% China Journal of Chinese Materia Medica 2009 34 3047-3050 Triterpenoid constituents in fruits of Psidum guajava SHU Jicheng, CHOU Guixin, WANG Zhengtao Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . myrianthic acid C30H48O6 ÏàËÆ¶È:57.5% China Journal of Chinese Materia Medica 2006 31 1875-1879 Triterpenes from herb of Potentilla chinesis LIU Pu, DUAN Hongquan, PAN Qin, ZHANG Yanwen, YAO Zhi Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . Primulagenin A ÏàËÆ¶È:57.5% Journal of Natural Products 1991 Vol 54 1044 Triterpenoid Saponins of Eleutherococcus senticosus Roots Ewa Segiet-Kujawa, Macki Kaloga Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . compound Ia ÏàËÆ¶È:57.5% Korean Journal of Pharmacognosy 1987 18(3) 188-190 A Triterpene Glycoside in Berries of Rubus coreanus Kim, Eun; Kim, Young-Choong Structure 13C NMR ̼Æ×Ä£Äâͼ |

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