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1 .     Repraesentin F
C15H24O3     ÏàËÆ¶È:66.6%
Bioscience, Biotechnology, and Biochemistry          2006          70          1502-1505
Repraesentins D, E and F, New Plant Growth Promoters from Lactarius repraesentaneus
Michiko KASHIWABARA, Tsunashi KAMO, Hidefumi MAKABE, Hisao SHIBATA and Mitsuru HIROTA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     oligandrumin C
C15H22O6     ÏàËÆ¶È:53.3%
Journal of Natural Products          2009          72          238-242
Sesquiterpenoids and Phenylpropanoids from Pericarps of Illicium oligandrum
Qin Zhu, Chun-Ping Tang, Chang-Qiang Ke, Wei Wang, Hai-Yan Zhang, and Yang Ye
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     eudesma-11-en-2¦Á,4¦Á-diol
    ÏàËÆ¶È:53.3%
Phytochemistry          2003          63          835-839
Eudesmane and megastigmane glucosides from Laggera alata
Qunxiong Zheng, Zhaojun Xu, Xianfeng Sun, Wei Yao, Handong Sun,Christopher H. K. Cheng, Yu Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     Eudesm-11-en-2,4¦Ádiol
C15H24O     ÏàËÆ¶È:53.3%
Phytochemistry          1993          34          567-568
Eudesm-11-en-2,4¦Á-diol from Nardostachys Chinensis
Koichi Masuyama, Hiroshi Morita, Koichi Takeya, Hideji Itokawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     Compound 4c
C26H40N4O6S     ÏàËÆ¶È:53.3%
Bioorganic & Medicinal Chemistry Letters          2006          16          2067-2070
Fluorescent glycosidase inhibiting 1,5-dideoxy-1,5-iminoalditols
Peter Greimel, Herwig Häusler, Inge Lundt, Karen Rupitz, Arnold E. St¨¹tz, Chris A. Tarling, Stephen G. Withers, Tanja M. Wrodnigg
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Subvellerolactones B
C15H22O5     ÏàËÆ¶È:53.3%
Bioorganic & Medicinal Chemistry Letters          2010          20          5385-5388
Lactarane sesquiterpenoids from Lactarius subvellereus and their cytotoxicity
Ki Hyun Kim, Hyung Jun Noh, Sang Un Choi, Ki Moon Park, Soon-Ja Seok, Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     dendronobilin J
C15H22O6     ÏàËÆ¶È:53.3%
Chinese Traditional and Herbal Drugs          2007          38          1771-1774
Sesquiterpenes from Dendrobium nobile
ZHANG Xue; GAO Hao; HAN Hui-ying; LIU Hong-wei; WANG Nai-li; YAO Xin-sheng; WANG Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     enokipodin G
C15H24O3     ÏàËÆ¶È:53.3%
Food Chemistry          2012          132          1346-1353
Bioactive sesquiterpenoids from the solid culture of the edible mushroom Flammulina velutipes growing on cooked rice
Yaqi Wang , Li Bao , Xiaoli Yang , Li Li , Shaifei Li , Hao Gao , Xin-Sheng Yao , Huaan Wen,Hong-Wei Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     compound 30
C15H31N3     ÏàËÆ¶È:53.3%
The Journal of Organic Chemistry          2002          67          245-258
Motuporamines, Anti-Invasion and Anti-Angiogenic Alkaloids from the Marine Sponge Xestospongia exigua (Kirkpatrick): Isolation, Structure Elucidation, Analogue Synthesis, and Conformational Analysis
David E. Williams, Kyle S. Craig, Brian Patrick, Lianne M. McHardy, Rob van Soest, Michel Roberge, and Raymond J. Andersen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     10,11-dihydrocyclonerotriol
C15H30O3     ÏàËÆ¶È:53.3%
Natural Product Communications          2014          9          313-314
Cyclonerol Derivatives from Trichoderma longibrachiatum YM311505
Qi-Cun Xuan, Rong Huang, You-Wei Chen, Cui-Ping Miao, Kai-Xia Ma, Tang Wang and Shao-Hua Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     pterocarpol
C15H26O2     ÏàËÆ¶È:53.3%
Natural Product Research and Development          2014          26          1593-1596
Chennical Constituents of Marine Fungus Penicillium sclerotiorum FS50
TAO Mei-hua, LI Le-jun, CHEN Yu-chan, HUO Guang-hua, ZHONG Wei-min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     cyperusol C
    ÏàËÆ¶È:53.3%
Natural Product Research and Development          2011          23          797-800
The Metabolites of Indolocarbazole Alkloids from the Marine-derived Streptomyces sp. SCSIO 1667
ZHOU, Jun-yong, HUANG, Hong-bo, WANG, Zhong-wen, YANG, Min-he, TIAN, Xin-peng, ZHANG, Si, ZHANG, Chang-sheng, JU, Jian-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     Atractylol A
C15H28O3     ÏàËÆ¶È:53.3%
Tetrahedron          2015          71          1909−1914
New sesquiterpenoids isolated from Atractylodes lancea fermented marine fungus
Hitoshi Kamauchi, Kaoru Kinoshita, Kazuhiko Takatori, Takashi Sugita, Kunio Takahashi, Kiyotaka Koyama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     compound 15b
C17H31NO3     ÏàËÆ¶È:52.9%
Tetrahedron          2003          59          7779-7786
Structures of new alkaloids sessilifoliamides A¨CD from Stemona sessilifolia
Daichi Kakuta, Yukio Hitotsuyanagi, Naofumi Matsuura, Haruhiko Fukaya, Koichi Takeya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     Ecliptamine C
C17H28N4O3     ÏàËÆ¶È:52.9%
Phytochemistry Letters          2015          11          224−228
Ecliptamines A¨CD, four new guanidine alkaloids from Eclipta prostrata L.
Akinori Tabata, Masahiko Taniguchi, Makio Shibano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     lannotinidine B
C16H25NO2     ÏàËÆ¶È:50%
Heterocycles          2009          77          679-729
The Lycopodium Alkaloids
Yusuke Hirasawa, Jun'ichi Kobayashi, and Hiroshi Morita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     2-hydroxycernuine
C16H27N2O2     ÏàËÆ¶È:50%
Biochemical Systematics and Ecology          2012          45          188-190
A new cernuane-type alkaloid from Lycopodium cernuum
S. Morel, I. Kerzaon, V. Roumy, N. Azaroual, S. Sahpaz, H. Joseph, F. Bailleul, T. Hennebelle
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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