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ħÁ¦ÄñÒø³æ (ÕýʽдÊÖ)
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΢ÆÕÊý¾ÝÇóÖú-B ÒÑÓÐ1È˲ÎÓë
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| 13C NMR (400MHz,DMSO) ¦Ä:14.60,16.71,20.38,24.57,25.56,27.45,28.15,30.93,32.08,40.15,44.57,45.55,48.22,68.91,72.23,94.19,123.84,129.36,130.14,135.70,168.03,206.99,209.09. |
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%(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½135¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . rel-(l' R,4' S,S' R)-2-(l'-Farnesyl)-4' ,5'-dihydroxy-2'-oxocyclohexan-1'-yl)-acetic acid ¦Ä-lactone C23H34O4 ÏàËÆ¶È:65.2% Phytochemistry 1995 40 1723-1728 Further farnesyl-homogentisic acid derivatives from Otoba parvifolia A. Gilberto Ferreira, João B. Fernandes, Paulo C. Vieira, Otto R. Gottlieb, Hugo E. Gottlieb Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3-(hydroxymethyl)-1,13,15-trihydroxy-7,11,15-trimethyl-2,6,10-hexadecatrien-14-yl acetate C22H38O6 ÏàËÆ¶È:60.8% Journal of Asian Natural Products Research 2012 14 652-656 Three new acyclic diterpenoids from Eupatorium lindleyanum DC. Shuang-Qing Wu, Nai-Yu Xu, Jian Zhang, Shi Yao & Chun-Jun Chu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . [1S-[1¦Á,2¦Á(Z),3¦Á,4¦Á]]-7-[3-[[[[(1-thioxoheptyl)amino]acetyl]amino]rnethyl]-7-oxabicyclo[2.2.1]hept-2-yl]-5-heptenoic acid C23H38N2O4S ÏàËÆ¶È:60.8% Journal of Medicinal Chemistry 1990 33 2465-2476 7-Oxabicyclo[2.2.1]heptyl carboxylic acids as thromboxane A2 antagonists: aza .omega.-chain analogs Masami Nakane, Joyce A. Reid, Wen Ching Han, Jagabandhu Das, Vu Chi Truc, Martin F. Haslanger, Dianne Garber, Don N. Harris, Anders Hedberg, Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . homaxinone A C19H28O2 ÏàËÆ¶È:56.5% Journal of Natural Products 2004 67 721-724 New Cytotoxic Metabolites from a Marine Sponge Homaxinella sp. Tayyab A. Mansoor, Jongki Hong, Chong-O. Lee, Chung Ja Sim, Kwang Sik Im, Dong Seok Lee, and Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (+)-17-oxocycloprotobuxine C23H37NO ÏàËÆ¶È:56.5% Journal of Natural Products 1999 62 665-669 New Steroidal Alkaloids from the Roots of Buxus sempervirens Atta-ur-Rahman, Athar Ata, Samina Naz, M. Iqbal Choudhary, Bilge Sener, and Songul Turkoz Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ent-7¦Á-acetoxy-3¦Â,12¦Á,17-trihydroxybeye¦Á-15-ene C22H34O5 ÏàËÆ¶È:56.5% Journal of Natural Products 1997 60 86-92 Biotransformation of ent-Atisenes and ent-Beyerenes by Rhizopus nigricans and Fusarium moniliforme Cultures Andr¨¦s Garc¨ªa-Granados, Andr¨¦s Parra, and Jos¨¦Mar¨ªa Arias Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3¦Â,11-dihydroxy-9,11-seco-5¦Á-pregna-11,20-dihydropyran-9-one 3-acetate C23H34O5 ÏàËÆ¶È:56.5% Steroids 2010 75 834-847 Synthesis of cytotoxic novel 9,11-secosterol analogs: Structure/activity studies Boonsong Kongkathip, Anuch Hasakunpaisarn, Suthinee Boonananwong, Ngampong Kongkathip Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 26 ÏàËÆ¶È:56.5% Phytochemistry 1998 47 1583-1600 Diterpenes from Euphorbia segetalis J. Jakupovic, F. Jeske, T. Morgenstern, F. Tsichritzis, J. A. Marco, W. Berendsohn Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . aphidicolin 17-acetate C22H26O5 ÏàËÆ¶È:56.5% Phytochemistry 1994 36 1551-1552 The isolation of 16¦Â, 18-dihydroxyaphidicolan-17-oic acid from Cephalosporium aphidicola James R. Hanson, Jacqueline A. Takahashi Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Henrylactone B C24H30O7 ÏàËÆ¶È:56.5% Planta Medica 2010 76 152-158 Henrylactones A¨CE and Anti-HBV Constituents from Illicium henryi Liu, Ji-Feng; Jiang, Zhi-Yong; Zhang, Quan; Shi, Yao; Ma, Yun-Bao; Xie, Ming-Jin; Zhang, Xue-Mei; Chen, Ji-Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 6 ÏàËÆ¶È:56.5% Acta Chemica Scandinavica 1986 40 855-860 Tobacco Chemistry. 63. Syntheses and Stereostructures of Six Tobacco Seco-Cembranoids. Wahlberg, Inger; Arndt, Rolf; Nishida, Toshiaki; Enzell, Curt R. Structure 13C NMR ̼Æ×Ä£Äâͼ |
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