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²éѯ½á¹û£º¹²²éµ½28¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 1a C21H30O7 ÏàËÆ¶È:68.1% Pharmaceutical Biology 1996 34 349-354 A New Quassinoid from Crude Quassin-extract of Quassia amara Dou J., McChesney J.D., Sindelar R.D., Goins D.K., Khan I.A., Walker L.A. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . (2S,4R,4aR,8R,8aR)-2-(4-Butoxy-3-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diol C22H32O5 ÏàËÆ¶È:66.6% Medicinal Chemistry Research 2014 23 5063−5073 Highly potent analgesic activity of monoterpene-derived (2S,4aR,8R,8aR)-2-aryl-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diols Irina Il¡¯ina, Oksana Mikhalchenko, Alla Pavlova, Dina Korchagina, Tat¡¯yana Tolstikova, Konstantin Volcho, Nariman Salakhutdinov, Evgeniy Pokushalov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (2S,4S,4aR,8R,8aR)-2-(4-(Hexyloxy)-3-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diol C24H36O5 ÏàËÆ¶È:66.6% Medicinal Chemistry Research 2014 23 5063−5073 Highly potent analgesic activity of monoterpene-derived (2S,4aR,8R,8aR)-2-aryl-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diols Irina Il¡¯ina, Oksana Mikhalchenko, Alla Pavlova, Dina Korchagina, Tat¡¯yana Tolstikova, Konstantin Volcho, Nariman Salakhutdinov, Evgeniy Pokushalov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . sequoiamonascin C C23H30O7 ÏàËÆ¶È:65.2% The Journal of Organic Chemistry 2003 68 4966-4969 Sequoiamonascins A-D: Novel Anticancer Metabolites Isolated from a Redwood Endophyte Donald B. Stierle, Andrea A. Stierle, and Timothy Bugni Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 9-deoxyisoxeniolide-A C20H28O3 ÏàËÆ¶È:63.6% Journal of Natural Products 2005 68 1336-1340 Xenia Diterpenoids from the Formosan Soft Coral Xenia blumi Ali A. H. El-Gamal, Chin-Ying Chiang, Shin-Huei Huang, Shang-Kwei Wang, and Chang-Yih Duh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 19-epi-isovoacristine C22H28N2O4 ÏàËÆ¶È:63.6% Chemical & Pharmaceutical Bulletin 1994 42 280-284 Two New Dimeric Indole Alkaloids from Tabernaemontana subglobosa MERR. from Taiwan Hiromitsu TAKAYAMA,Shinya SUDA,Ih-Sheng CHEN,Mariko KITAJIMA,Norio AIMI and Shin-ichiro SAKAI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 9-deoxyxeniolide-A C20H28O3 ÏàËÆ¶È:63.6% Natural Product Research 1995 6 49-55 Antibacterial Diterpenoids from an Undescribed Soft-Coral of the genus Xenia H¨¦l¨¨ne C. Vervoor; William Fenical Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . (E) 16-epiaffinisine C20H24N2O ÏàËÆ¶È:63.6% Phytochemistry 1991 30 3785-3792 Alkaloids from leaves and root bark ofErvatamia hirta Pascale Clivio, Bernard Richard, Jean-Robert Deverre, Thierry Sevenet, Monique Zeches, Louisette Le Men-Oliver Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . denudatine ÏàËÆ¶È:63.6% Journal of China Pharmaceutical University 2003 34 17-20 Chemical Studies on Aconitum Kirinense Nakai FENG Feng; LIU Wen Yuan; CHEN You Sheng; YE Wen Cai; LIU Jing Han; ZHAO Shou Xun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 3-Methoxy-17a,17b-dihomoestra-1,3,5(10),16-tetraen-17b¦Â-ol C21H28O2 ÏàËÆ¶È:63.6% Steroids 2012 77 110-117 Increasing the amphiphilicity of an estradiol based steroid structure by Barbier-allylation ¨C ring-closing metathesis ¨C dihydroxylation sequence Tiina Saloranta, Istv¨¢n Zupk¨®, Jani Rahkila, Gyula Schneider, J¨¢nos Wölfling, Reko Leino Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 3-Methoxy-17a,17b-dihomoestra-1,3,5(10)-trien-16¦Â,17¦Â,17b¦Â-triol C21H30O4 ÏàËÆ¶È:63.6% Steroids 2012 77 110-117 Increasing the amphiphilicity of an estradiol based steroid structure by Barbier-allylation ¨C ring-closing metathesis ¨C dihydroxylation sequence Tiina Saloranta, Istv¨¢n Zupk¨®, Jani Rahkila, Gyula Schneider, J¨¢nos Wölfling, Reko Leino Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 3-Methoxy-17a,17b-dihomoestra-1,3,5(10)-trien-16¦Á,17¦Á,17b¦Â-triol C21H30O4 ÏàËÆ¶È:63.6% Steroids 2012 77 110-117 Increasing the amphiphilicity of an estradiol based steroid structure by Barbier-allylation ¨C ring-closing metathesis ¨C dihydroxylation sequence Tiina Saloranta, Istv¨¢n Zupk¨®, Jani Rahkila, Gyula Schneider, J¨¢nos Wölfling, Reko Leino Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . (2'R)-1-[4-(n-butyl)-2,5-dimethyl-1,3-dioxo-2-(4-cyclopentenyl)methyl]-3-(2-hydroxyethyl)indoline C22H27O3N ÏàËÆ¶È:63.6% Tetrahedron 2005 61 6015-6039 Determination of the absolute stereochemistry and asymmetric total synthesis of madindolines A and B: a practical improvement to a second-generation approach from the first-generation Tomoyasu Hirose, Toshiaki Sunazuka, Daisuke Yamamoto, Naoto Kojima, Tatsuya Shirahata, Yoshihiro Harigaya, Isao Kuwajima, Satoshi ¨mura Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . sphaeropsidin F C20H32O4 ÏàËÆ¶È:63.6% Australian Journal of Chemistry 2003 56 615-619 Sphaeropsidin F, a New Pimarane Diterpene Produced in Vitro by the Cypress Pathogen Sphaeropsis sapinea f. sp. Cupressi Antonio Evidente , Lorenzo Sparapano, Anna Andolfi, Giovanni Bruno and Andrea Motta Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . daphnicyclidin C C22H25NO5 ÏàËÆ¶È:63.6% Journal of the American Chemical Society 2001 123 11402-11408 Daphnicyclidins A−H, Novel Hexa- or Pentacyclic Alkaloids from Two Species of Daphniphyllum Jun'ichi Kobayashi, Yasutada Inaba, Motoo Shiro, Naotoshi Yoshida, and Hiroshi Morita Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . Dimethyl (2E,6Z)-2-[(3'Z,7'E)-9'-hydroxy-4',8'-dimethylnona-3',7'-di enyl]-6-methylocta-2,6-dienedioate C22H32O4 ÏàËÆ¶È:63.6% Australian Journal of Chemistry 1981 34 1491-1499 The chemistry of Eremophila spp. XV. New acyclic diterpenes from Eremophila spp EL Ghisalberti, PR Jefferies and GM Proudfoot Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . vinmajine E C23H26N2O5 ÏàËÆ¶È:63.6% Tetrahedron 2014 70 8723-8729 Indole alkaloids from cultivated Vinca major Gui-Guang Cheng, Yun-Li Zhao, Yu Zhang, Paul-Keilah Lunga, Dong-Bao Hu, Yan Li, Ji Gu, Chang-Wei Song, Wei-Bang Sun, Ya-Ping Liu, Xiao-Dong Luo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 3-Methoxy-17-(N-phenyl-carboxamido)-13¦Á-estra-1,3,5(10),16-tetraene C26H29O2N ÏàËÆ¶È:62.5% Steroids 2008 73 669-675 The synthesis of 17-alkoxycarbonyl- and 17-carboxamido-13¦Á-estra-1,3,5(10),16-tetraene derivatives via palladium-catalyzed carbonylation reactions |

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