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(24R)-cycloartane-3¦Â,24,25-triol ÏàËÆ¶È:76.6% Phytochemistry 1994 35 1017-1022 Cycloartane triterpene from Juncus effusus Marina Della Greca, Antonio Molinaro, Pietro Monaco and Lucio Previtera Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . cycloartanol ÏàËÆ¶È:76.6% The Chinese Pharmaceutical Journal 2003 55 267-272 The Cytotoxic Constitunets of Euphorbia makinoi Jing-Ru Weng, Huey-Jen Su, Ming-Hong Yen, Shen-Jeu Won and Chun-Nan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 19 ÏàËÆ¶È:76.6% Planta Medica 2011 77 736-741 Chemical Constituents and Antitubercular Activity of Formosan Pisonia umbellifera Hsiou-Ting Kuo, Chien-Fang Peng, Hung-Yi Huang, Chu-Hung Lin, Ih-Sheng Chen, Ian-Lih Tsai Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Neoabiestrine H C30H52O4 ÏàËÆ¶È:76.6% Phytochemistry 2012 81 159-164 Cytotoxic triterpenoids from Abies recurvata Yong-Li Li, Yan-Xia Gao, Xian-Wen Yang, Hui-Zi Jin, Ji Ye, Luke Simmons, Ning Wang, Andre Steinmetz, Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . schisanterpene B C27H40O4 ÏàËÆ¶È:75% Chemical & Pharmaceutical Bulletin 2006 54(4) 542-545 A New Triterpene and Dibenzocyclooctadiene Lignans from Schisandra propinqua (WALL.) BAILL LiJia XU,Feng HUANG,SiBao CHEN,ShiLin CHEN,and PeiGen XIAO Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 24-Methylene-3,4-seco-cycloart-4(28)-en-3-oic acid ÏàËÆ¶È:74.1% Archives of Pharmacal Research 2001 24 527-531 A cytotoxic secocycloartenoid fromAbies koreana Hyun Jung Kim, Quoc Khanh Le, Mi Hyun Lee, Tae Sung Kim and Hyeong-Kyu Lee, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Abiesatrine I C31H54O3 ÏàËÆ¶È:74.1% Organic & Biomolecular Chemistry 2010 8 2609-2616 Abiesatrines A¨CJ: anti-inflammatory and antitumor triterpenoids from Abies georgei Orr Xian-Wen Yang, Su-Mei Li, Liang Wu, Yong-Li Li, Lin Feng, Yun-Heng Shen, Jun-Mian Tian, Jian Tang, Ning Wang, Yonghong Liu and Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 11 ÏàËÆ¶È:74.1% Journal of Natural Medicines 2014 68 513-520 3,4-seco-24-homo-28-nor-Cycloartane and drimane-type sesquiterpenes and their lactams from the EtOAc-soluble fraction of a leaf extract of Cinnamosma fragrans and their biological activity Yuya Nomoto, Liva Harinantenaina, Sachiko Sugimoto, Katsuyoshi Matsunami, Hideaki Otsuka Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . nigranoic acid ÏàËÆ¶È:73.3% Chemistry & Biodiversity 2007 Vol. 4 112 Hydroxylation of the Triterpenoid Nigranoic Acid by the Fungus Gliocladium roseum YMF1.00133 Jin-Yan Dong, Ye-Gao Chen, Hong-Chuan Song, Yan-Hui Zhu, Yong-Ping Zhou, Lei Li, Yan-Ping H, Jie Cao, and Ke-Qin Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . secaubrytriol C30H50O5 ÏàËÆ¶È:73.3% Journal of Natural Products 2006 69 1711-1714 seco-Cycloartane Triterpenes from Gardenia aubryi Raphal Grougnet, Prokopios Magiatis, Sofia Mitaku, Stella Loizou, Paraskevi Moutsatsou, Aris Terzis, Pierre Cabalion, Franois Tillequin, and Sylvie Michel Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . cycloart-24-en-3¦Â,23(R),28-triol 3-sulfate C30H49O6S ÏàËÆ¶È:73.3% Journal of Natural Products 2000 63 210-216 New Triterpenoid Sulfates from the Red Alga Tricleocarpa fragilis1 F. David Horgen, Bryan Sakamoto, and Paul J. Scheuer Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 3¦Â,28-dihydroxycycloart-24-en-23-one 3-sulfate C30H47O6S ÏàËÆ¶È:73.3% Journal of Natural Products 2000 63 210-216 New Triterpenoid Sulfates from the Red Alga Tricleocarpa fragilis1 F. David Horgen, Bryan Sakamoto, and Paul J. Scheuer Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 25-hydroxyl-9,19-cycloart-22-ene-3-one C30H48O2 ÏàËÆ¶È:73.3% Journal of Asian Natural Products Research 2009 11 779-782 Two new triterpenoids from the leaves and stems of Fritillaria hupehensis Hui-Fang Pi, Peng Zhang, Han-Li Ruan, Yong-Hui Zhang, Han-Dong Sun and Ji-Zhou Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (24R)-cycloartane-3¦Â,24,25,28-tetrol C30H52O4 ÏàËÆ¶È:73.3% Phytochemistry 1997 46 397-381 Cycloartane triterpenoids from Aglaia harmsiana Akira Inada, Shintaro Ohtsuki, Takako Sorano, Hiroko Murata, Yuka Inatomi, Dedy Darnaedi, Tsutomu Nakanishi Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (24R)-cycloartane-3¦Á,24,25-triol C30H52O3 ÏàËÆ¶È:73.3% Phytochemistry 1997 46 397-381 Cycloartane triterpenoids from Aglaia harmsiana Akira Inada, Shintaro Ohtsuki, Takako Sorano, Hiroko Murata, Yuka Inatomi, Dedy Darnaedi, Tsutomu Nakanishi Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (24R)-cycloartane-3¦Â,24,25-triol ÏàËÆ¶È:73.3% Phytochemistry 1997 46 397-381 Cycloartane triterpenoids from Aglaia harmsiana Akira Inada, Shintaro Ohtsuki, Takako Sorano, Hiroko Murata, Yuka Inatomi, Dedy Darnaedi, Tsutomu Nakanishi Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Gardenoin H C30H48O3 ÏàËÆ¶È:73.3% Chemical & Pharmaceutical Bulletin 2011 59(3) 385-387 Gardenoins E-H, Cycloartane Triterpenes from the Apical Buds of Gardenia obtusifolia Thanesuan NUANYAI, Ruengrit SAPPAPAN, Tirayut VILAIVAN, and Khanitha PUDHOM Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Nigranoic acid ÏàËÆ¶È:73.3% Phytochemistry Letters 2012 5 123-127 Microbial transformation of the triterpene nigranoic acid in Trichoderma sp. Yu-Hong Yang,Rong Sun,Hong-Chuang Song,Yao-Bo Xu,Pan Yang,Dong-Yan Yang,Ze-Kai Shen,An-Ran Wang,Ye-Gao Chen,Jin-Yan Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . Nigranoic acid C30H46O4 ÏàËÆ¶È:73.3% Archives of Pharmacal Research 2003 26 912-916 Triterpenoids from Schisandra henryi with cytotoxic effect on leukemia and hela cells in vitro Ye-Gao Chen, Zheng-Cai Wu, Yu-Ping Lv, Shi-Hong Gui and Jin Wen, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . Abiesatrine J C30H44O4 ÏàËÆ¶È:73.3% Organic & Biomolecular Chemistry 2010 8 2609-2616 Abiesatrines A¨CJ: anti-inflammatory and antitumor triterpenoids from Abies georgei Orr Xian-Wen Yang, Su-Mei Li, Liang Wu, Yong-Li Li, Lin Feng, Yun-Heng Shen, Jun-Mian Tian, Jian Tang, Ning Wang, Yonghong Liu and Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . compound 11 ÏàËÆ¶È:73.3% Tetrahedron 2002 58 8073-8086 Cytotoxic and anti-HIV-1 constituents of Gardenia obtusifolia and their modified compounds Patoomratana Tuchinda, Wilart Pompimon, Vichai Reutrakul, Manat Pohmakotr, Chalobon Yoosook, Natedao Kongyai, Samaisukh Sophasan, Kulawee Sujarit, Suchart E Upathum, Thawatchai Santisuk Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . coccinetane A C30H48O2 ÏàËÆ¶È:73.3% Tetrahedron 1999 55 119-132 Novel seco-cycloartanes from Kadsura coccinea and the assisted autoxidation of a tri-substituted alkene Lai-King Sy, Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . compound 14 C30H50O ÏàËÆ¶È:73.3% Tetrahedron 1999 55 119-132 Novel seco-cycloartanes from Kadsura coccinea and the assisted autoxidation of a tri-substituted alkene Lai-King Sy, Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . compound 11 C30H46O3 ÏàËÆ¶È:73.3% Tetrahedron 2002 58 8073-8086 Cytotoxic and anti-HIV-1 constituents of Gardenia obtusifolia and their modified compounds Patoomratana Tuchinda, Wilart Pompimon, Vichai Reutrakul, Manat Pohmakotr, Chalobon Yoosook, Natedao Kongyai, Samaisukh Sophasan, Kulawee Sujarit, Suchart E Upathum, Thawatchai Santisuk Structure 13C NMR ̼Æ×Ä£Äâͼ |

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