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monkey514: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ·Ç³£¸Ðл£¡ 2013-03-12 10:54:52
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1 . tormentic acid ÏàËÆ¶È:62.0% Phytochemistry 1992 31 3909-3914 Triterpenoids from plants of the sanguisorbeae Gesa Reher, Miloš Bud¨§š¨ªnsky Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . nervoyan B C24H42O6 ÏàËÆ¶È:54.1% Biochemical Systematics and Ecology 2011 39 700-703 Phytane and neoclerodane diterpenes from the aerial parts of Inula nervosa Wall. Lan Yan, Xiang Rong Cheng, Qi Zeng, Jiang Jiang Qin, Wei Dong Zhang, Hui Zi Jin Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . aphidicolin ÏàËÆ¶È:54.1% Journal of the Brazilian Chemical Society 2011 22 80-85 Biosynthesis of Aphidicolin Proceeds via the Mevalonate Pathway in the Endophytic Fungus Nigrospora sphaerica Adriana A. Lopes and Mônica T. Pupo Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (4R*,5R*,9S*,10R*,11Z)-4-methoxy-9-((dimethylamino)-methyl)-12,15-epoxy-11(13)-en-decahydrona phthalen-16-ol C24H43O3N ÏàËÆ¶È:54.1% Marine Drugs 2012 10 1619-1630 A Great Barrier Reef Sinularia sp. Yields Two New Cytotoxic Diterpenes Anthony D. Wright, Jonathan L. Nielson, Dianne M. Tapiolas, Catherine H. Liptrot and Cherie A. Motti Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ursolic acid ÏàËÆ¶È:53.8% Food Chemistry 2011 124 468-475 Analysis of the anti-inflammatory properties of Rosmarinus officinalis L. in mice Juc¨¦lia Pizzetti Beninc¨¢, Juliana Bastos Dalmarco, Moacir Geraldo Pizzolatti, Tania Silvia Fröde Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Asiatic acid ÏàËÆ¶È:51.8% Archives of Pharmacal Research 2005 28 1135-1141 Inhibitory effect on TNF-¦Á-induced IL-8 production in the HT29 cell of constituents from the leaf and stem ofWeigela subsessilis Phuong Thien Thuong, WenYi Jin, JongPill Lee, RackSeon Seong and Young-Mi Lee, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (25S)-5¦Á-cholestane-3¦Â,4¦Â,6¦Á,7¦Á,8,15¦Á,16¦Â,26-octo1 ÏàËÆ¶È:51.8% European Journal of Organic Chemistry 1988 1988 1185-1189 Biologically active glycosides from asteroidea, XVIII. 1H-NMR spectroscopy and biological activities of polyhydroxylated steroids from the starfish Asterina pectinifera M¨¹ller et Troschel Ryuichi Higuchi, Yuko Noguchi, Tetsuya Komori and Takuma Sasaki Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (3¦Á,4¦Â,14RS)-neoclerod-13(16)-ene-3,4,14,15-tetrol C20H36O4 ÏàËÆ¶È:50% Helvetica Chimica Acta 2004 Vol. 87 1279 Neoclerodane Diterpenes from Amoora stellato-squamosa Shu-Min Yang, Shao-Hua Wu, Xiang-Dong Qin, Xiao-Dong Luo, and Da-Gang Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ent-2¦Á,15,16,19-tetrahydroxypima¦Á-8(14)-ene C20H34O4 ÏàËÆ¶È:50% Journal of Natural Products 2004 67 1517-1521 Novel Diterpenoids and Diterpenoid Glycosides from Siegesbeckia orientalis Ying Xiang, Hua Zhang, Cheng-Qi Fan, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . malacosterone C27H44O8 ÏàËÆ¶È:50% Phytochemistry 1998 49 2109-2114 Ecdysteroid constituents of the mushroom Tapinella panuoides Karel Vok¨¢, Milo Budnsky, Juraj Harmath¦Á, Jitka Kohoutov¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ursolic acid ÏàËÆ¶È:50% Phytochemistry 1992 31 3909-3914 Triterpenoids from plants of the sanguisorbeae Gesa Reher, Miloš Bud¨§š¨ªnsky Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound-3 ÏàËÆ¶È:50% Phytochemistry 1988 27 2205-2208 Sesquiterpene glycosides based on the alloaromaden-drane skeleton from Calendula arvensis Cosimo Pizza,Nunziatina De Tommasi Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 4a ÏàËÆ¶È:50% Journal of the Chemical Society, Perkin Transactions 1 1989 823-826 Structure elucidation of (22E,24R,25R)-24-methyl-5¦Á-cholest-22-ene-3¦Â,4¦Â,5,6¦Á,8,14,15¦Á,25,26-nonaol and (22E,24S)-24-methyl¨C5¦Á-cholest-22-ene-3¦Â,4¦Â,5,6¦Á,8,14,15¦Á,25,28-nonaol, minor marine polyhydroxysteroids isolated from the starfish Archaster typicus Raffaele Riccio, Mos¨¦ Santaniello, Olinda Squillace Greco and Luigi Minale Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . AP1 ÏàËÆ¶È:50% Natural Toxins 1999 7 31-38 Oxidative deamination of hydrolyzed fumonisin B1 (AP1) by cultures of Exophiala spinifera Barbara A. Blackwell, Jacob T. Gilliam, Marc E. Savard, J. David Miller and Dr. Jonathan P. Duvick Structure 13C NMR ̼Æ×Ä£Äâͼ |

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