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1 . pinnatifone B C15H18O3 ÏàËÆ¶È:93.3% Chemical & Pharmaceutical Bulletin 2014 62 1009-1012 Sesquiterpenoids and Lignans from the Roots of Syringa pinnatifolia Ze-Ming Zhang, Chun-Hua Wang, Xiao-Jie Zeng, Qiu Qiu, Wei Tang, Guo-Qiang Li, Yao-Lan Li, Guo-Cai Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . ligujapone C14H14O2 ÏàËÆ¶È:60% Natural Product Research and Development 2009 21 776-778 Chemical Constituents of the Roots of Ligularia fischeri DENG Mei-cai; JIAO Wei; DONG Wei-wei; LU Run-hua Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . Faveline C18H22O2 ÏàËÆ¶È:55.5% Tetrahedron Letters 1991 32 3083-3086 Favelines, novel tricyclic benzocycloheptenes with cytotoxic activities from brazilian plant, doscolus phyllacanthus Yuichi Endo, Tomihisa Ohta, Shigeo Nozoe Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . strobilol F C15H22O3 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2008 Vol. 91 1595 Cadinane-Type Sesquiterpenoids, Strobilols E¨CK, from the Liquid Culture of Strobilurus ohshimae Fuminori Hiramatsu, Tetsuya Murayama, Takuya Koseki, Katsuhide Okada, and Yoshihito Shiono Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 3¦Á-hydroxy-11¦Á,13-dihydrodehydrocostuslactone ÏàËÆ¶È:53.3% Journal of Asian Natural Products Research 2006 8 713-718 Microbial transformation of dehydrocostuslactone by Mucor polymorphosporus X.-C. MA, L.-J. WU and D.-A. GUO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 1¦Á,5¦Á-dihydroxyeudesm-4(15)-en-6¦Â,11¦ÂH-12,6-olide ÏàËÆ¶È:53.3% Phytochemistry 1994 37 477-485 Sesquiterpene lactones from North African Artemisia species J.Alberto Marco, Juan F. Sanz-Cervera, Jose M. Pareja, Felix Sancenon, Joan Valles-Xirau Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . Zerumbone ÏàËÆ¶È:53.3% Phytochemistry 1980 19 2643-2650 Cytotoxic components of Zingiber zerumbet, Curcuma zedoaria and C. domestica H.W.D. Matthes, B. Luu, G. Ourisson Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . ligujapone C14H16O2 ÏàËÆ¶È:53.3% Bulletin of the Chemical Society of Japan 1990 63 2239-2245 Sesquiterpenes from the Rhizomes of Ligularia dentata Hara Keizo Naya, Tohru Okayama, Masaaki Fujiwara, Makoto Nakata, Tsutomu Ohtsuka, Seiko Kurio Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . eremophilone ÏàËÆ¶È:53.3% Phytochemistry 2011 72 400-408 Chemical composition and cytotoxicity of oils and eremophilanes derived from various parts of Eremophila mitchellii Benth. (Myoporaceae) Karren D. Beattie, Peter G. Waterman, Paul I. Forster, Dion R. Thompson, David N. Leach Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦Â-Vetispirene ÏàËÆ¶È:53.3% Flavour and Fragrance Journal 2000 15 395-412 Constituents of Haitian vetiver oil Peter Weyerstahl, Helga Marschall, Ute Splittgerber, Dietmar Wolf and Horst Surburg Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 12-methoxy-9(10¡ú20)-abeo-16,17-bis-nor-abieta-8',10'(20),11,13-tetraen-17-one C19H24O2 ÏàËÆ¶È:52.6% Journal of the Brazilian Chemical Society 1991 2 105-110 Terpenoids from Cnidoscolus phyllacanthus Pax et Hoff . Telma L.G. de Lemos, Edilberto R. Silveira, Mailcar F. Oliveira, Raimundo Braz Filho and Charles D. Hufford. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . acetate of ligujapone C15H18O2 ÏàËÆ¶È:50% Bulletin of the Chemical Society of Japan 1990 63 2239-2245 Sesquiterpenes from the Rhizomes of Ligularia dentata Hara Keizo Naya, Tohru Okayama, Masaaki Fujiwara, Makoto Nakata, Tsutomu Ohtsuka, Seiko Kurio Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 11,14-Dihydroxy-7-oxo-16-devinyl-ent-pimara-8,11,13-trien-17-oic acid C18H22O5 ÏàËÆ¶È:50% Journal of Natural Products 2014 77 2342-2351 Anti-inflammatory Diterpenoids from the Root Bark of Acanthopanax gracilistylus Zhi-Yuan Wu, Yi-Bei Zhang, Kong-Kai Zhu, Cheng Luo, Jing-Xian Zhang, Chun-Ru Cheng, Rui-Hong Feng, Wen-Zhi Yang, Feng Zeng, Yang Wang, Ping-Ping Xu, Ji-Ling Guo, Xuan Liu, Shu-Hong Guan, and De-An Guo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-03-02 21:25:54
jiandanai187
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1 . pinnatifone B C15H18O3 ÏàËÆ¶È:93.3% Chemical & Pharmaceutical Bulletin 2014 62 1009-1012 Sesquiterpenoids and Lignans from the Roots of Syringa pinnatifolia Ze-Ming Zhang, Chun-Hua Wang, Xiao-Jie Zeng, Qiu Qiu, Wei Tang, Guo-Qiang Li, Yao-Lan Li, Guo-Cai Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . ligujapone C14H14O2 ÏàËÆ¶È:60% Natural Product Research and Development 2009 21 776-778 Chemical Constituents of the Roots of Ligularia fischeri DENG Mei-cai; JIAO Wei; DONG Wei-wei; LU Run-hua Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . Faveline C18H22O2 ÏàËÆ¶È:55.5% Tetrahedron Letters 1991 32 3083-3086 Favelines, novel tricyclic benzocycloheptenes with cytotoxic activities from brazilian plant, doscolus phyllacanthus Yuichi Endo, Tomihisa Ohta, Shigeo Nozoe Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2015-03-02 21:31:39














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