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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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6Â¥: Originally posted by jiyannangxj at 2015-04-07 22:59:34
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6Â¥: Originally posted by jiyannangxj at 2015-04-07 22:59:34
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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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