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14.3, 23.3, 27.8, 28.1, 29.3, 30.2, 30.2, 30.4, 30.4, 30.5, 30.6, 30.8, 33.1, 56.9, 95.5, 114.4, 123.9, 130.7, 130.8, 141.8, 143.3, 148.9, 171.0
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yjl2007: ½ð±Ò+10 2014-08-08 15:24:11
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1 .     ardisiphenol B
C23H36O4     ÏàËÆ¶È:65.2%
Chemical & Pharmaceutical Bulletin          2002          50(11)          1484-1487
Ardisiphenols and Other Antioxidant Principles from the Fruits of Ardisia colorata
Megumi SUMINO,Toshikazu SEKINE, Nijsiri RUANGRUNGSI,Kazuei IGARASHI,and Fumio IKEGAMI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     O-oleyl-L-glutamine
C23H42N2O4     ÏàËÆ¶È:65.2%
Tetrahedron          1999          55          11275-11280
New fatty acid amides from regurgitant of Lepidopteran (Noctuidae, Geometridae) caterpillars
Georg Pohnert, Verena Jung, Erkki Haukioja, Kyösti Lempa, Wilhelm Boland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     tornabeatin B
C24H42O3     ÏàËÆ¶È:62.5%
Phytochemistry          2004          65          2605-2612
The tornabeatins, four tetrahydro-2-furanone derivatives from the lichenized ascomycete Tornabea scutellifera (With.) J.R. Laundon
Tom¨¢š Řezanka, Marina Temina, Lum¨ªr Hanuš, Valery M. Dembitsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     tornabeatin A
C22H38O3     ÏàËÆ¶È:60.8%
Phytochemistry          2004          65          2605-2612
The tornabeatins, four tetrahydro-2-furanone derivatives from the lichenized ascomycete Tornabea scutellifera (With.) J.R. Laundon
Tom¨¢š Řezanka, Marina Temina, Lum¨ªr Hanuš, Valery M. Dembitsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     N-linolyl-L-glutamine
C23H40N2O4     ÏàËÆ¶È:60.8%
Tetrahedron          1999          55          11275-11280
New fatty acid amides from regurgitant of Lepidopteran (Noctuidae, Geometridae) caterpillars
Georg Pohnert, Verena Jung, Erkki Haukioja, Kyösti Lempa, Wilhelm Boland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     N-linolyl-L-glutamate
C22H39NO5     ÏàËÆ¶È:60.8%
Tetrahedron          1999          55          11275-11280
New fatty acid amides from regurgitant of Lepidopteran (Noctuidae, Geometridae) caterpillars
Georg Pohnert, Verena Jung, Erkki Haukioja, Kyösti Lempa, Wilhelm Boland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     1,4-dideoxy-5-O-[(9Z)-octadec-9-en-1-yl]-1,4-imino-D-ribitol
C23H45NO3     ÏàËÆ¶È:60.8%
Bioorganic & Medicinal Chemistry          2011          19          7720-7727
Anti-cancer activity of 5-O-alkyl 1,4-imino-1,4-dideoxyribitols
Claudia Bello, Giovanna Dal Bello, Michele Cea, Aimable Nahimana, Dominique Aubry, Anna Garuti, Giulia Motta, Eva Moran, Floriana Fruscione, Paolo Pronzato, Francesco Grossi, Franco Patrone, Alberto Ballestrero, Marc Dupuis, Bernard Sordat, Kaspar Zimmermann, Jacqueline Loretan, Markus Wartmann, Michel A. Duchosal, Alessio Nencioni, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     gerronemin B
C24H32O4     ÏàËÆ¶È:56.5%
Phytochemistry          2002          59          643-648
Gerronemins A¨CF, cytotoxic biscatechols from a Gerronema species
Sven Silberborth, Anja Stumpf, Gerhard Erkel, Timm Anke, Olov Sterner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     gerronemin D
C26H36O4     ÏàËÆ¶È:56.5%
Phytochemistry          2002          59          643-648
Gerronemins A¨CF, cytotoxic biscatechols from a Gerronema species
Sven Silberborth, Anja Stumpf, Gerhard Erkel, Timm Anke, Olov Sterner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     gerronemin F
C28H38O4     ÏàËÆ¶È:56.5%
Phytochemistry          2002          59          643-648
Gerronemins A¨CF, cytotoxic biscatechols from a Gerronema species
Sven Silberborth, Anja Stumpf, Gerhard Erkel, Timm Anke, Olov Sterner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     1-methyl-2-[(Z)-7-tridecenyl]-4(1H)-quinolone
    ÏàËÆ¶È:56.5%
Phytochemistry          1996          43          719-722
Quinolone alkaloids from Evodia rutaecarpa
Yuan-Qing Tang, Xiao-Zhang Feng, Liang Huang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     1-methyl-2-[(Z)-7-tridecenyl]-4(1H)-evocarpine
    ÏàËÆ¶È:56.5%
Phytochemistry          1996          43          719-722
Quinolone alkaloids from Evodia rutaecarpa
Yuan-Qing Tang, Xiao-Zhang Feng, Liang Huang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     Compound 1b
C24H46N3O2     ÏàËÆ¶È:56.5%
Bioorganic & Medicinal Chemistry Letters          2007          17          4584-4587
Design, synthesis, and preliminary biological evaluation of a novel triazole analogue of ceramide
Sanghee Kim, Minjae Cho, Taeho Lee, Sukjin Lee, Hye-Young Min, Sang Kook Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     (2S,3R,2'S,4E)-2'-hydroxy-C4-ceramide
C22H49NO4     ÏàËÆ¶È:56.5%
Bioorganic & Medicinal Chemistry          2010          18          7565-7579
Synthesis, NMR characterization and divergent biological actions of 2'-hydroxy-ceramide/dihydroceramide stereoisomers in MCF7 cells
Zdzislaw M. Szulc, Aiping Bai, Jacek Bielawski, Nalini Mayroo, Doreen E. Miller, Hanna Gracz, Yusuf A. Hannun, Alicja Bielawska
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     N-palmitoleyl-L-glutamine
C21H38N2O4     ÏàËÆ¶È:56.5%
Tetrahedron          1999          55          11275-11280
New fatty acid amides from regurgitant of Lepidopteran (Noctuidae, Geometridae) caterpillars
Georg Pohnert, Verena Jung, Erkki Haukioja, Kyösti Lempa, Wilhelm Boland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     7,8-dihydroxy-3-decyl-4-methylcoumarin
C20H28O4     ÏàËÆ¶È:56.5%
Bioorganic & Medicinal Chemistry          2009          17          1550-1556
Specificities of Calreticulin Transacetylase to acetoxy derivatives of 3-alkyl-4-methylcoumarins: Effect on the activation of nitric oxide synthase
Abha Kathuria, Anjali Gupta, Nivedita Priya, Prabhjot Singh, Hanumantharao G. Raj, Ashok K. Prasad, Virinder S. Parmar, Sunil K. Sharma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (S)-N-(12-aminododecyl)-4-hydroxy-¦Á-[(1-oxobutyl)amino]benzenepropanamide trifluoroacetate
    ÏàËÆ¶È:56.5%
Journal of Medicinal Chemistry          2000          43          4526-4533
Solid-Phase Synthesis and Biological Evaluation of a Combinatorial Library of Philanthotoxin Analogues
Kristian Strømgaard, Tim J. Brier, Kim Andersen, Ian R. Mellor, Alex Saghyan, Denis Tikhonov, Peter N. R. Usherwood, Povl Krogsgaard-Larsen, and Jerzy W. Jaroszewski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     (E)-9-octadecenoic acid
C18H34O2     ÏàËÆ¶È:56.5%
Journal of Agricultural and Food Chemistry          2002          50          6993-6996
Repellent Activity of Constituents Identified in Foeniculum vulgare Fruit against Aedes aegypti (Diptera:  Culicidae)
Do-Hyoung Kim, Soon-Il Kim, Kyu-Sik Chang, and Young-Joon Ahn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     linoleic acid
C18H32O2     ÏàËÆ¶È:56.5%
Chinese Journal of Medicinal Chemistry          2012          22          47-50
Chemical constituents of Lysimachia stenosepala
CAO Xian-ping; LIANG Xin; ZHONG Hui-min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     N-(3,5-Dimethoxy-4-hydroxy-E-cinnamoyl)-L-tyrosine Dodecyl Ester
C32H45NO7     ÏàËÆ¶È:55.5%
Journal of Agricultural and Food Chemistry          2003          51          4596-4602
Synthesis of Lipophilic Clovamide Derivatives and Their Antioxidative Potential against Lipid Peroxidation
Jakob P. Ley and Heinz-J¨¹rgen Bertram
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     (E)-2,11,12,13,15,16-Hexachloro-14-hydroxytetracos-1-en-1-yl sulfate
C24H41Cl6O5S     ÏàËÆ¶È:54.1%
Journal of Natural Products          2010          73          279-283
Structure Revision and Absolute Configuration of Malhamensilipin A from the Freshwater Chrysophyte Poterioochromonas malhamensis
Alban R. Pereira, Tara Byrum, Grant M. Shibuya, Christopher D. Vanderwal and William H. Gerwick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     tert-butyl {(4R,5S)-4-[8'-(2''-hexyl-1'',3''-dioxolan-2''-yl)octyl]-5-(hydroxymethyl)-2,2-dimethyl-1,3-dioxan-5-yl}carbamate
C29H55NO7     ÏàËÆ¶È:54.1%
Chemical Papers          2013          67          1317-1329
Stereoselective total synthesis of protected sulfamisterin and its analogues
Jana Špakov¨¢ Raschmanov¨¢, Miroslava Martinkov¨¢*, Jozef Gonda, Alena Uhr¨ªkov¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     1-oleoyl-3-O-¦Â-D-galactopyranosyl-sn-glycerol
    ÏàËÆ¶È:53.8%
Chinese Pharmaceutical Journal          2006          41          1374-1375
Studies on Non-Alkaloid Constituent of Amaryllidaceae Species Hippeastrun vittatum(L'Herit.) Herb.
WANG Guang-shu, WANG Ling-yan, YANG Xiao-hong, XU Jingda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     1-O-11'-(Z)-icosen-1'-ynyl-2-hydroxy-sn-glycero-3-phosphoethanolamine
C25H48NO6P     ÏàËÆ¶È:53.5%
Bioorganic & Medicinal Chemistry          2014          22          2966-2973
Synthesis and evaluation of immunostimulant plasmalogen lysophosphatidylethanolamine and analogues for natural killer T cells
Guanghui Ni, Zhiyuan Li, Kangjiang Liang, Ting Wu, Gennaro De Libero, Chengfeng Xia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     Alkylresorcinol B
    ÏàËÆ¶È:52.1%
Chemical & Pharmaceutical Bulletin          2002          50(11)          1484-1487
Ardisiphenols and Other Antioxidant Principles from the Fruits of Ardisia colorata
Megumi SUMINO,Toshikazu SEKINE, Nijsiri RUANGRUNGSI,Kazuei IGARASHI,and Fumio IKEGAMI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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