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²éѯ½á¹û£º¹²²éµ½127¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 3¡ä-O-¦Â-D-glucopyranosyl ligustroside C31H42O17 ÏàËÆ¶È:100% Heterocycles 2009 77 557-563 Secoiridoid Di-glycosides from Osmanthus ilicifolius Shigeaki Sakamoto, Koichi Machida, and Masao Kikuchi Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . excelside B C31H42O17 ÏàËÆ¶È:93.5% Journal of Natural Products 2010 73 2-6 Iridoids from Fraxinus excelsior with Adipocyte Differentiation-Inhibitory and PPAR¦Á Activation Activity Naisheng Bai, Kan He, Alvin Ibarra, Antoine Bily, Marc Roller, Xiaozhuo Chen and Ralph Rhl Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¡ä-O-¦Â-D-glucopyranosyl 10-hydroxyligustroside C31H42O18 ÏàËÆ¶È:93.5% Heterocycles 2009 77 557-563 Secoiridoid Di-glycosides from Osmanthus ilicifolius Shigeaki Sakamoto, Koichi Machida, and Masao Kikuchi Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3¡ä-O-¦Â-D-glucopyranosyl oleuropein C31H42O18 ÏàËÆ¶È:90.3% Heterocycles 2009 77 557-563 Secoiridoid Di-glycosides from Osmanthus ilicifolius Shigeaki Sakamoto, Koichi Machida, and Masao Kikuchi Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3¡ä-O-¦Â-D-glucopyranosyl 10-acetoxyligustroside C33H44O19 ÏàËÆ¶È:87.8% Heterocycles 2009 77 557-563 Secoiridoid Di-glycosides from Osmanthus ilicifolius Shigeaki Sakamoto, Koichi Machida, and Masao Kikuchi Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . angustifolioside B C31H42O17 ÏàËÆ¶È:87.0% Phytochemistry 1993 33 1453-1456 Secoiridoids from Fraxinus angustifolia Ihsan Cäliş, Mohammed Hosny, Taha Khalifa, Sansei Nishibe Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Excelside B C31H42O17 ÏàËÆ¶È:87.0% Chemical & Pharmaceutical Bulletin 2011 59 803-833 Naturally Occurring Iridoids and Secoiridoids. An Updated Review, Part 4 Biswanath DINDA, Sudhan DEBNATH, and Rajarshi BANIK Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (8E)-n¨¹zhenide ÏàËÆ¶È:83.8% Chemical & Pharmaceutical Bulletin 2002 50(4) 493-497 Studies on the Constituents of Syringa Species. X. Five New Iridoid Glycosides from the Leaves of Syringa reticulata (BLUME) HARA Koichi MACHIDA, Atsuko KANEKO, Tomokazu HOSOGAI, Rie KAKUDA, Yasunori YAOITA, and Masao KIKUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . angustifolioside A C31H48O12 ÏàËÆ¶È:80.6% Phytochemistry 1993 33 1453-1456 Secoiridoids from Fraxinus angustifolia Ihsan Cäliş, Mohammed Hosny, Taha Khalifa, Sansei Nishibe Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . oleonuezhenide ÏàËÆ¶È:80.6% Chinese Pharmaceutical Journal 2011 46 259-262 Chemical Constituents from the Fruits of Ligustrum lucidum FENG Zhi-yi, FENG Jing, CUI Ying Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (8E)-nuezhenide ÏàËÆ¶È:80.6% Chemistry & Biodiversity 2013 10 96-128 Chemical Constituents and Biological Activities of Plants from the Genus Ligustrum Bei-Bei Gao, Gai-Mei She and Dong-Mei She Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Safghanoside F C38H48O18 ÏàËÆ¶È:79.4% Chemical & Pharmaceutical Bulletin 2007 55 689-728 Naturally Occurring Secoiridoids and Bioactivity of Naturally Occurring Iridoids and Secoiridoids. A Review, Part 2 Biswanath DINDA, Sudhan DEBNATH and Yoshihiro HARIGAYA Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 3¡ä-O-¦Â-D-glucopyranosyl 10-acetoxyoleuropein C33H44O20 ÏàËÆ¶È:78.7% Heterocycles 2009 77 557-563 Secoiridoid Di-glycosides from Osmanthus ilicifolius Shigeaki Sakamoto, Koichi Machida, and Masao Kikuchi Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . nuezhenide ÏàËÆ¶È:77.4% Chinese Pharmaceutical Journal 2011 46 259-262 Chemical Constituents from the Fruits of Ligustrum lucidum FENG Zhi-yi, FENG Jing, CUI Ying Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (8E)-Å®Õê×ÓÜÕ C31H42O17 ÏàËÆ¶È:77.4% Chinese Journal of Medicinal Chemistry 2007 17 173-177 Isolation and identification of iridoid glycosides from Ilex pubescens YANG Xin, DING Yi, ZHANG Dong-ming Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (8E)-Å®Õê×ÓÜÕ ÏàËÆ¶È:77.4% Chinese Traditional and Herbal Drugs 2011 42 1894-1899 Chemical constituents from seeds of Syringa oblata ZHANG, Shu-jun, GUO, Hua-qiang, HAN, Jing, ZHAO, Ming, WANG, Jin-lan Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 1'''-O-¦Â-D-glucosylfraxiformoside C38H48O18 ÏàËÆ¶È:76.4% Phytochemistry 1994 35 177-181 Secoiridoid glucosides from Fraxinus malacophylla He Zheng-Dan, Shinichi Ueda, Kenichiro Inoue, Masako Akaji, Tetsuro Fujita, Yang Chong-Ren Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . framoside ÏàËÆ¶È:75% Phytochemistry 1998 49 1329-1332 Secoiridoid glucosides from fraxinus ornus bark Tanya Iossifov¦Á, Bernhard Vogler, Ivanka Kostova Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . framoside C32H38O13 ÏàËÆ¶È:75% Phytochemistry 1993 32 133-136 Five secoiridoid glucosides from Fraxinus formosana Takao Tanahashi, Hiroko Watanabe, Atsuko Itoh, Naotaka Nagakura, Kenichiro Inoue, Masami Ono, Tetsuro Fujita, Masanori Morita, Cheng-chang Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 3'-O-¦Â-D-glucopyranosylsyringopicroside C30H40O16 ÏàËÆ¶È:74.1% Chemical & Pharmaceutical Bulletin 2002 50(4) 493-497 Studies on the Constituents of Syringa Species. X. Five New Iridoid Glycosides from the Leaves of Syringa reticulata (BLUME) HARA Koichi MACHIDA, Atsuko KANEKO, Tomokazu HOSOGAI, Rie KAKUDA, Yasunori YAOITA, and Masao KIKUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ |

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²»ÖªÊÇʲôÔÒò£¬¸Õ¸ÕÓÖË¢ÐÂÁ˼¸´Î²éµ½Á˼¸¸öÊý¾Ý¡£ ²éѯ½á¹û£º¹²²éµ½16¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ent-labd-8(17),13-dien-15,16-olide-19 oic acid(pinusolidic acid) ÏàËÆ¶È:58.8% Asian Journal of Chemistry 2012 24 784-786 Phytochemical Investigation of the Stem Bark of Phlogacanthus thyrsiflorus (Roxb.) Nees. S. ILHAM, *, M.S. ALI and C.M. HASAN Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3,4-epoxy-11¦Á,13-dihydroelemen-12, 8-olide C15H22O3 ÏàËÆ¶È:53.3% Journal of Natural Products 2001 64 466-471 Sesquiterpenes and Monoterpenes from the Bark of Inula macrophylla Bao-Ning Su,Yoshihisa Takaishi, Tetsuya Yabuuchi, Takenori Kusumi, Motoo Tori,Shigeru Takaoka,Gisho Honda, Michiho Ito, Yoshio Takeda, Olimjon K. Kodzhimatov, and Ozodbek Ashurmetov Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . cytokine-induced neutrophil chemoattractant(CINC-1) ÏàËÆ¶È:53.3% Planta Medica 1998 64 454-455 Reynosin from Sassurea lappa as Inhibitor on CINC-1 Induction in LPS-Stimulated NRK-52E Cells Jee H. Jung, Joo Young Ha, Kyung Rak Mm,Futoshi Shibata, Hideo Nakagawa, Sam Sik Kang,Il-Moo Chang, and Youngsoo Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . N-(2-(2-Methyl-1H-indol-3-yl)ethyl)butyramide C15H20N2O ÏàËÆ¶È:53.3% Tetrahedron 2012 68 813-818 A one-pot three-component reaction for the preparation of highly functionalized tryptamines Se Jeong Yeo, Yongxiang Liu, Xiang Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 8-{2-[4-(4-fluorophenyl)piperazin-1-yl]ethyl}-8-azaspiro[4¡¤5]decane-7,9-dione ÏàËÆ¶È:53.3% Journal of Medicinal Chemistry 2005 48 3076-3079 Synthesis and Structure−Activity Relationship of Fluoro Analogues of 8-{2-[4-(4-Methoxyphenyl)piperazin-1yl]ethyl}-8-azaspiro[4.5]decane-7,9-dione as Selective ¦Á1d-Adrenergic Receptor Antagonists Michael J. Konkel, John M. Wetzel, Marie Cahir, Douglas A. Craig, Stewart A. Noble, and Charles Gluchowski Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . cis-2-isopropenyl-1-(4'-methyl-4'-penten-1'-yl)cyclobutane-acetonitrile ÏàËÆ¶È:53.3% European Journal of Organic Chemistry 1999 1999 1201-1211 Syntheses of Cyclobutane Derivatives: Total Synthesis of (+) and (¨C) Enantiomers of the Oleander Scale Aspidiotus nerii Sex Pheromone François-Didier Boyer and Paul-Henri Ducrot Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 6a-hydroxyeudesma-4(15),7(11),8(9)-trien-12,8-olide C15H18O3 ÏàËÆ¶È:53.3% Chemistry & Biodiversity 2014 11 919-928 Sesquiterpenoids from Chloranthus henryi and Their Anti-neuroinflammatory Activities Li-Jun Wang, Juan Xiong, Shu-Ting Liu, Xin-Hua Liu and Jin-Feng Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (1R,6S)-6-(((6-oxocyclohex-1-en-1-yl)methoxy)carbonyl)cy-clohex-3-enecarboxylic acid C15H18O5 ÏàËÆ¶È:53.3% Tetrahedron 2014 70 9064-9069 Organocatalytic desymmetrization of cyclic meso-anhydrides through enantioselective alcoholysis with functionalized primary nitroallylic alcohols Yan ming Chen, Mamatha Amireddy, Kwunmin Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 8(17), 13-ent-labdadien-15¡ú16-lactone-19-oic acid C20H28O4 ÏàËÆ¶È:50% Phytochemistry 2003 1309-1317 ent-Labdane diterpenes from the aquatic plant Potamogeton pectinatus Patrice Waridel, Jean-Luc Wolfender, Jean-Bernard Lachavanne, Kurt Hostettmann Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . andrograpanin C20H30O3 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1984 32 2117-2125 On the Diterpenoids of Andrographis paniculata : X-Ray Crystallographic Analysis of Andrographolide and Structure Determination of New Minor Diterpenoids TETSURO FUJITA,RYUJIRO FUJITANI,YOSHIO TAKEDA,YOSHIHISA TAKAISHI,TOSHIHIDE YAMADA,MASARU KIDO and IWAO MIURA Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 8(17),13-labdadien-16,15-olid-19-pic acid(demethylpinusolide) C20H28O4 ÏàËÆ¶È:50% Korean Journal of Pharmacognosy 1998 29(4) 347-352 Diterpenes of Biota orientalis Leaves Sung, Sang-Hyun; Koo, Kyung-Ah; Lim, Hye-Kyung; Lee, Heum-Sook; Cho, Jung-Hee; Kim, Hye-Soo; Kim, Young-Choong Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 2-(4-chlorophenyl)-4¦Á-ethyl-3a¦Á,4¦Â,5,8b¦Á-tetrahydro-2H,6H-pyrrolo[3,4-e]indole-1,3-dione C18H17ClN2O2 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2009 46 1154-1176 Access to indoles via Diels-Alder reactions of 2-vinylpyrroles with maleimides Wayland E. Noland,Nicholas P. Lanzatella,Lakshmanan Venkatraman,Nicholas F. Anderson and Glen C. Gullickson Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 3a-allyl-5-methoxy-1,8-dimethyl-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole C16H22N2O ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2012 20 4901-4914 Synthesis of phenserine analogues and evaluation of their cholinesterase inhibitory activities Masashi Shinada, Fuminori Narumi, Yuji Osada, Koji Matsumoto, Takayasu Yoshida, Kazuhiro Higuchi, Tomomi Kawasaki, Hiroyuki Tanaka, Mitsutoshi Satoh Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (3aS*,8S*,8aR*)-dimethyl 6-isopropyl-4-methylene-8-(trie-thoxysilyl)-3,3a,4,5,8,8a-hexahydroazulene-2,2(1H)-dicarboxylate C24H40O7Si ÏàËÆ¶È:50% Tetrahedron 2013 69 7826-7830 Stereoselective rhodium-catalyzed [(3+2)+2] carbocyclization reaction of trialkoxysilyl-substituted alkenylidenecyclopropanes with monosubstituted alkynes P. Andrew Evans, Tomass Baikstis, Phillip A. Inglesby Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . andrographolide-3-O-sulfate C20H30O8S ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2004 52 772-775 Four New Andrographolide Metabolites in Human Urine Liang Cui, Feng Qiu, Naili Wang, Xinsheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 14-sulfo isoandrographolide 3-sulfate C20H30O10S2 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2003 51 586-589 Six New Andrographolide Metabolites in Rats Xiangjiu He, Jiankuan Li, Hao Gao, Feng Qiu, Xiangmin Cui, Xinsheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ |

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