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1 .     cerevisterol
    ÏàËƶÈ:96.5%
Helvetica Chimica Acta          2007          Vol. 90          1165
New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori
Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     6,9-epoxyergosta-7,22-dien-3-ol
    ÏàËƶÈ:96.5%
Acta Botanica Sinica          2002          44          1239-1242
Chemical Constituents of One Species of Endophytic Fungus in Taxus chinensis
ZHANGJi-Hui, GUO Shun-Xing YANGJun-Shan, XIAO Pei-Gen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     6,9-Epoxy-ergosta-7,22-dien-3¦Â-ol
    ÏàËƶÈ:96.5%
Biochemical Systematics and Ecology          2007          35          790-793
Triterpenes and steroids from Armillaria mellea Vahl. ex Fr.
Wen-Juan Guo, Shun-Xing Guo, Jun-Shan Yang, Xiao-Mei Chen, Pei-Gen Xiao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     5¦Á,6¦Á-epoxy-24(R)-methylcholesta-7,22-dien-3¦Â-ol
C28H44O2     ÏàËƶÈ:96.5%
Phytochemistry          1999          51          891-898
Antitumor sterols from the mycelia of Cordyceps sinensis
Jin Woo Bok, Leonard Lermer, Jeff Chilton, Hans G. Klingeman, G.H. Neil Towers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     ergosta-7,22-diene-2¦Â,3¦Á,9¦Á-triol
C28H46O3     ÏàËƶÈ:96.5%
Journal of Natural Products          1991          Vol 54          998
Novel Cytotoxic Principles of Formosan Ganoderma lucidum
Chun-Nan Lin, Whey-Pim Tome, Shen-Jeu Won
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     6,9-epoxy-ergosta-7,22-dien-3-ol
C28H44O2     ÏàËƶÈ:96.5%
Acta Pharmaceutica Sinica          2000          Vol 35          367-369
THE STEROL CONSTITUENTS OF MYCENA DENDROBII
CHEN Xiao Mei; YANG Jun Shan; GUO Shun Xing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     5,6-Epoxy-22-en-3-ol-ergosterol
C28H44O2     ÏàËƶÈ:96.5%
Chemical Research in Chinese Universities          1998          14          270-272
Chemical Constituent of Natural Body of Armillaria mellea and Structure of 5, 6-Epoxy-22-en-3-ol-ergosterol
SHI Lei, CAO Rui-min, LU Shi-xiang and WU Guang-xuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     cerevisterol (3¦Â,5¦Á,6¦Â-trihydroxyergosta-7,22-diene)
    ÏàËƶÈ:96.5%
Phytochemistry          1988          27          2777-2779
Cytotoxic steroids from the mushroom Agaricus blazei
Hirokazu Kawagishi,Ryosuke Katsumi,Toshimi Sazawa,Takashi Mizuno,Toshihiko Hagiwara,Takuji Nakamura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     ergosta-6,22-dien-3¦Â,5¦Â,8¦Â-triol
    ÏàËƶÈ:96.5%
Chinese Traditional and Herbal Drugs          2000          31          328-330
ºÖÔ²¿×Å£¸Î¾ú»¯Ñ§³É·ÖµÄÑо¿
Íò»Ô
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:96.5%
Chinese Journal of Medicinal Chemistry          2005          15          221-223
The chemical constituents from the mycel ia of marine fungus Rhizopus sp.
SHI Ying, TIAN Li, PEI Yue-hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     5¦Á,6¦Á-epoxy-24(R)-methylcholesta-7,22-dien-3¦Â-ol
    ÏàËƶÈ:96.5%
Chinese Journal of Medicinal Chemistry          2008          18          452-456
Secondary metabolites produced by Fusarium sp. 2TnP1-2, an endophytic fungus from Trewia nudif lora
DU Zhi-zhi, SONG Cheng-zhi, YU Bu-zhu, LUO Xiao-dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:96.5%
Natural Product Research and Development          2006          18          238-242
Chemical Study on Porandra scandens
HE Zhi-heng; LUO Ying-gang; LI Hong-juan£¨; ZHANG Guo-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:96.5%
Natural Product Research and Development          2006          18          411-414
Phytochemical Study on Zehneria maysorensis
LI Hong-juan;LUO Ying-gang; HE Zhi-heng; ZHANG Guo-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     ergosta-6,22-dien-3¦Â,5¦Â,8¦Â-triol
    ÏàËƶÈ:96.5%
Natural Product Research and Development          1999          11(6)          18-21
THREE STEROLS FROM GYROPORUS CASTANEUS
Wan Hui; Sun Rongqi; Wu Dajun; Guo Beishu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     ergosta-7,22-diene-2¦Â,3¦Á,9¦Á-triol
    ÏàËƶÈ:96.5%
Phytotherapy Research          2011          25          1579-1585
Ergosta-7,22-diene-2¦Â,3¦Á,9¦Á-triol from the Fruit Bodies of Ganoderma lucidum Induces Apoptosis in Human Myelocytic HL-60 Cells
Mi Kyoung Lee, Tran Manh Hung, To Dao Cuong, MinKyun Na, Jin Cheol Kim, Eun-Jung Kim, Hee-Sung Park, Jae Sue Choi, IkSoo Lee, KiHwan Bae, Masao Hattori and Byung Sun Min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     cerevisterol
    ÏàËƶÈ:96.5%
Journal of Guangdong Phamaceutical University          2011          27          256-259
Chemical constituents of the mycelia of Guignardia mangiferae,an endophyte from Smilax glabra
LIANG Fa-liang, LI Dong-li, TAO Mei-hua, ZHANG De-zhi, ZHANG Wei-min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
C28H44O2     ÏàËƶÈ:96.5%
Natural Medicines          1996          50          179-181
Sterol Constituents from the Sclerotium of Polyporus umbellatus Fries
OHTA KOJI,YAOITA YASUNORI,MATSUDA NORIKO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     (22E)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:96.5%
Chinese Journal of Marine Drugs          2012          31          5-10
Studies on chemical constituents of the South China Sea Gorgonian Rumphella aggregata
LIU Cai-xia; LI Ping-lin; TANG Xu-li; LI Guo-qiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     cerevisterol
    ÏàËƶÈ:96.5%
Mycosystema          2010          29          249-253
Steroids from fruiting bodies of Coprinus comatus and their inhibition to tumor cell proliferation
FENG Na; ZHANG Jing-Song TANG Qing-Jiu HAO Rui-Xia LIU Yan-Fang YANG Yan JIA Wei ZHOU Shuai TANG Chuan-Hong ZHONG Jian-Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:96.5%
Chinese Traditional and Herbal Drugs          2012          43          664-666
Studies on chemical constituents of Lasiosphaera fenzlii
SU Ming-zhi; LUO Zhou; YAN Ming; ZHAO Qing-chun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     22E-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËƶÈ:96.5%
Journal of Shenyang Pharmaceutical University          2012          29          678-684
A new disecosteroid from an endolichenic fungal stain Sporormiella irregularis(No.71-11-4-1)
LI Yan-jun; LI Xiao-xia; CHEN Guo-dong; GAO Hao; GUO Liang-dong; YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     (22E,24S)-cerevisterol
    ÏàËƶÈ:96.5%
Journal of Chinese Medicinal Materials          2005          28          998-999
²èË‘×ÓÒ¶¿×¾ú»¯Ñ§³É·ÖµÄÑо¿
ÁõÓñºì, ÐìÁè´¨, Íõ½¨Æ½, Ìï¾°Õñ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     ergost-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:96.5%
Journal of Chinese Medicinal Materials          2010          33          1262-1265
Studies on the Chemical Constituents from Petroleum Ether Portion of Abelmoschus esculentus
JIA Lu, LI Dong, JING Lin-lin, GUO Ming-ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     cerevisterol
    ÏàËƶÈ:96.5%
Journal of Chinese Medicinal Materials          2011          34          549-551
Studies on the Secondary Metabolites of Coriolopsis sp.G066
SANG Zhi-gao, LI Dong-li, TAO Mei-hua, ZHANG Wei-min, TU Guo-quan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     3¦Â,5¦Á,6¦Â-ÈýôÇ»ù-(22E,24R)-Âó½ÇçÞ-7,22-¶þÏ©
    ÏàËƶÈ:96.5%
Journal of Tropical and Subtropical Botany          2011          19          75-78
Steroidal Metabolites of Fimetariella rabenhorstii,Endophytic Fungus from Aquilaria sinensis
TAO, Meihua, YAN, Jian, WEI, Xiaoyi, LI, Dongli, ZHANG, Weimin, TAN, Jianwen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     cerevisterol
    ÏàËƶÈ:93.1%
Phytochemistry          1997          44          1443-1448
Cytochalasins and phytotoxins from the fungus Xylaria obovata
Dawit Abate, Wolf-Rainer Abraham, Holger Meyer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     22E,24R)-ergost-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:93.1%
Academic Journal of Second Military Medical University          2010          31          421-424
Studies on chemical constituents of Anthogorgia sp.
XU Yuan-yuan, LI Ling, YI Yang-hua, ZHANG Wen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:93.1%
Chinese Traditional and Herbal Drugs          2011          42          31-33
Chemical constituents of Dendrobium crystallinum
WANG Lei, ZHANG Chao-feng, WANG Zheng-tao, ZHANG Mian, XU Luo-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     Ergosta-7,22-dien-3¦Â,5¦Á,6¦Á-triol
C28H46O3     ÏàËƶÈ:93.1%
Journal of Anhui Agricultural Sciences          2010          38          2356-2357
Research on the Chemical Componen ts of the Fruit Bodies ofBoletus calopus
ZUOW ei et al
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     (3¦Â,5¦Á,6¦Â,22E)-Âó½ÇçÞ-7,22-¶þÏ©-3,5,6-Èý´¼
C28H46O3     ÏàËƶÈ:93.1%
Chinese Journal of Antibiotics          2011          36          576-580
Antibacterial metabolites from the endophytic fungus R7 of Aquilaria sinensis
Wei, Jing, Dai, Hao-Fu, Yu, Lei, Wang, Hui, and, Mei, Wen-Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     3¦Â,16¦Â,30-trihydroxycycloart-20,24-diene
C30H52O3     ÏàËƶÈ:90%
Zeitschrift f¨¹r Naturforschung C          2002          57          489-495
Microbial Transformation of a Mixture of Argentatin A and Incanilin
Key words: Argentatin A, Incanilin, Biotransformation
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     (3¦Â,5¦Á,6¦Â,22E)-6-methoxyergosta-7,22-diene-3,5-diol
    ÏàËƶÈ:89.6%
Helvetica Chimica Acta          2007          Vol. 90          1165
New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori
Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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33 .     (22E,24R)-23-methylergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
C29H48O3     ÏàËƶÈ:89.6%
Chemical & Pharmaceutical Bulletin          1999          47          847-851
Sterol Constituents from Seven Mushrooms
Yasunori YAOITA,Makiko ENDO,Yoshino TANI,Kaori MACHIDA,Keiko AMEMIYA,Katsuyuki FURUMURA and Masao KIKUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     biemnasterol
C28H44O3     ÏàËƶÈ:89.6%
Journal of Natural Products          1993          Vol 56          2016
Biemnasterol, a New Cytotoxic Sterol with the Rare 22,25-Diene Side Chain, Isolated from the Marine Sponge Biemna sp.
Chun-min Zeng, Masami Ishibashi, Jun'ichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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35 .     3¦Â,5¦Á-dihydroxy-6¦Â-methoxyergosta-7,22-diene
C29H48O3     ÏàËƶÈ:89.6%
Phytochemistry          1988          27          2777-2779
Cytotoxic steroids from the mushroom Agaricus blazei
Hirokazu Kawagishi,Ryosuke Katsumi,Toshimi Sazawa,Takashi Mizuno,Toshihiko Hagiwara,Takuji Nakamura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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36 .     (24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:89.6%
Chinese Pharmaceutical Journal          2006          41          1131-1133
Chemical Constituents of Monascus anka
LI Li-li, CHEN Jie-peng, KONG Ling-yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     (22E,24R)-rgosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:89.6%
Natural Product Research and Development          2007          19          610-613
Chemical Constituents from Schizophyllum commune
MAO Shao-chun; LI Zhu-ying; LI Cong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     6-methoxy-cerevisterol
    ÏàËƶÈ:89.6%
Natural Product Research and Development          2007          19          605-609
Study on the Chemical Constitutes of Hydnellum concrescens
YANG Xiao-long;WANG Fei; SHAO Hong-jun; DONG Ze-jun; DING Zhi-hui; YANG Wan-qiu; LIU Ji-kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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39 .     ergosta-7,22-dien-3,5,6-triol
C28H46O3     ÏàËƶÈ:89.6%
Academic Journal of Second Military Medical University          2007          28          266-271
Isolation,identification,and biological characterization of 6 secondary metabolites extracted from Myxococcus xanthus 095B06
SHI Xiao-qiong, XU Qiang-zhi, LIU Xiao-yu, HAN Wen-ju, LIU Xin-li, JIAO Bing-hua, LI Yue-zhong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     22E-6¦Â-methoxyergosta-7,22-diene-3¦Â,5¦Á-diol
C29H48O3     ÏàËƶÈ:89.6%
Journal of Shenyang Pharmaceutical University          2012          29          678-684
A new disecosteroid from an endolichenic fungal stain Sporormiella irregularis(No.71-11-4-1)
LI Yan-jun; LI Xiao-xia; CHEN Guo-dong; GAO Hao; GUO Liang-dong; YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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41 .     (22E,24R)-6-Acetoxy-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:86.6%
Natural Product Communications          2009          4          1449-1454
Ring B Aromatic Steroids from an Endophytic Fungus, Colletotrichum sp.
Wen Zhang , Siegfried Draeger, Barbara Schulz and Karsten Krohn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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42 .     (22E,24R)-6-Acetoxy-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:86.6%
Natural Product Communications          2009          4          1449-1454
Ring B Aromatic Steroids from an Endophytic Fungus, Colletotrichum sp.
Wen Zhang , Siegfried Draeger, Barbara Schulz and Karsten Krohn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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43 .     ergost-5,22-dien-3¦Â,7¦Â-diol
C28H46O2     ÏàËƶÈ:86.2%
Chinese Traditional and Herbal Drugs          2005          36          510-511+550
Å£¶ú¶ä»¯Ñ§³É·ÖµÄÑо¿
²ÌÏ麣,µËµÂɽ,ÂíÔƱ£,ÂÞÏþ¶«
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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44 .     8,9-epoxyergosta-5,22-dien-3¦Â,15-diol
C28H44O3     ÏàËƶÈ:86.2%
Journal of the Chinese Chemical Society          1991          38          71-76
Studies on the Constituents of Ganoderma lucidum
½ªºêÕÜ(Hung-Cheh Chiang);ÖìÊÀ²ý(Shih-Chang Chu)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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45 .     cholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:86.2%
Journal of Chinese Medicinal Materials          2006          29          555-557
Chemical Constituents from the South China Sea Gorgonian Coral Subergorgia reticulata
YANG Jin, QI Shu-hua, ZHANG Si, LI Qing-xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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46 .     (22E,24R)-6¦Â-¼×Ñõ»ùÂó½ÇçÞ-7,22-¶þÏ©-3¦Â,5¦Á-¶þ´¼
    ÏàËƶÈ:86.2%
Journal of Chinese Medicinal Materials          2008          31          1343-1347
Studies on the Anti-tumor Activity Principles of a Marine-derived Fungus BZYT-21
GAO Zong-hua, MA Li-ying, SHEN Yun-xiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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47 .     5¦Á,6¦Á-epoxy-24(R)-methylcholesta-7,22-dien-3¦Â-ol
C28H44O2     ÏàËƶÈ:86.2%
Guihaia          2011          31          699-701
Chemical constituents of endophyte Talaromyces sp.T1BF from Taxus yunnanensis
LI, Liang-Qun, YANG, Yan-Guang, ZENG, Ying, ZOU, Cheng, ZHAO, Pei-Ji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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48 .     3¦Â-acteoxy-(22E, 24R)-24-methyl-5¦Á-cholest-7, 22-diene-5, 6¦Â-diol
C30H48O4     ÏàËƶÈ:83.3%
Acta Botanica Yunnanica          2002          24(4)          125-128
The Chemical Constituents from Basidiocarps of Sarcodon aspratum
HUANG Yue,DONG Ze-Jun,LIU Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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49 .     5,6¦Â-Dihydroxy-5¦Á-ergosta-7,22-dien-3¦Â-ylacetate
C30H48O4     ÏàËƶÈ:83.3%
Steroids          2006          71          565-577
Regio and stereoselective oxidations of unsaturated steroidal compounds with H2O2 mediated by CH3ReO3
Francesco P. Ballistreri, Rosa Chillemi, Sebastiano Sciuto, Gaetano A. Tomaselli, Rosa M. Toscano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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50 .     cerevisterol
C28H46O3     ÏàËƶÈ:82.7%
Acta Botanica Yunnanica          2006          28(3)          315-318
A New Steroidal Glycoside from the Fruiting Bodies of Tylopilus virens (Boletaceae)
WANG Fei,ZHANGLing, DONG Ze-Jun,LIU Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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51 .     (22E)-27-nor-24-methyl-5(-cholesta-7, 22-diene-3¦Â, 5, 6¦Â-triol
C27H44O3     ÏàËƶÈ:82.7%
Acta Botanica Yunnanica          2002          24(4)          125-128
The Chemical Constituents from Basidiocarps of Sarcodon aspratum
HUANG Yue,DONG Ze-Jun,LIU Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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52 .     ergosta-7,22-diene-3,5,6-triol
C28H46O3     ÏàËƶÈ:82.7%
Chemistry of Natural Compounds          2009          45          124-125
COMPONENTS OF THE SCLEROTIAOF Polyporus umbellatus
Weiwei Zhou, Shunxing Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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53 .     stigmasta-7,22-diene-3¦Â,5¦Á,6¦Á-triol,respectively
C28H46O3     ÏàËƶÈ:82.7%
Chinese Chemical Letters          2006          17          481-484
An Abietane Diterpene and a Sterol from Fungus Phellinus igniarius
Ying WANG, Su Juan WANG, Shun Yan MO, Shuai LI, Yong Chun YANG, Jian Gong SHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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54 .     (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol (=cerevisterol)
    ÏàËƶÈ:82.7%
Steroids          2001          66          771-775
A novel sterol from Chinese truffles Tuber indicum
Gao Jinming, Hu Lin, Liu Jikai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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55 .     5¦Á,6¦Á-Epoxy-26,27-dinorergosta-7,22-en-3¦Â-ol
C26H40O2     ÏàËƶÈ:82.7%
Steroids          2008          73          568-573
A series of new 5,6-epoxysterols from a Chinese sponge Ircinia aruensis
Shihai Xu, Xiaojian Liao, Bin Du, Xulong Zhou, Qichang Huang, Chumei Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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56 .     5¦Á,6¦Á-Epoxyergosta-7-en-3¦Â-ol
C28H46O2     ÏàËƶÈ:82.7%
Steroids          2008          73          568-573
A series of new 5,6-epoxysterols from a Chinese sponge Ircinia aruensis
Shihai Xu, Xiaojian Liao, Bin Du, Xulong Zhou, Qichang Huang, Chumei Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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57 .     5¦Á,6¦Á-Epoxystigmasta-7-en-3¦Â-ol
C29H48O2     ÏàËƶÈ:82.7%
Steroids          2008          73          568-573
A series of new 5,6-epoxysterols from a Chinese sponge Ircinia aruensis
Shihai Xu, Xiaojian Liao, Bin Du, Xulong Zhou, Qichang Huang, Chumei Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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58 .     ergosta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:82.7%
Journal of Asian Natural Products Research          2005          7          165-169
Sterols from the pericarp of Sphaerophysa salsula DC
GUO-YU LI, JIN-HUI WANG and XIAN LI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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59 .     stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËƶÈ:82.7%
Natural Product Research          2008          22          154-166
Antifouling and antibacterial compounds from the gorgonians Subergorgia suberosa and Scripearia gracillis
S. H. Qi; S. Zhang; L. H. Yang; P. Y. Qian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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60 .     6,9-epidioxyergosta-7,22-dien-3¦Â-ol
    ÏàËƶÈ:82.7%
China Journal of Chinese Materia Medica          2007          32          235-237
Studies on chemical constituents from the fruiting bodies of Ganoderma sinense Zhao,Xu et Zhang
LIU Chao , WANG Hongqing, LI Baoming, CHEN Ruoyun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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61 .     (22E,24R)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol
    ÏàËƶÈ:82.7%
Journal of Natural Products          1987          Vol 50          915
Four New Trihydroxylated Sterols from the Sponge Spongionella gracilis Four New Trihydroxylated Sterols from the Sponge Spongionella gracilis
Vincenzo Piccialli, Donato Sica
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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62 .     cerevisterol(3¦Â,5¦Á,6¦Â-trihydroxyergosta-7,22-diene)
C28H46O3     ÏàËƶÈ:82.7%
Phytochemistry          1991          30          4117-4120
Glycosides of ergosterol derivatives from Hericum erinacens
Yoshihisa Takaishi, Minoru Uda, Takashi Ohashi, Kimiko Nakano, Koutarou Murakami, Toshiaki Tomimatsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

63 .     5¦Á,6¦Á-epoxys-tigmasta-7-en-3¦Â-ol
    ÏàËƶÈ:82.7%
Chinese Journal of Marine Drugs          2009          28(4)          21-25
Studies on chemical constituents of marine sponge Aplysinopsis sp.
LI Xue, SONG Shao-jiang, PIAO Shu-juan, DONG Tao, LIN Hou-wen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

64 .     ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËƶÈ:82.7%
Indian Journal of Chemistry          2005          44B          1291-1294
Sterols and flavonol glycosides from Melothria purpusila
Langoljam,Reena D; Kongbrailatpam,Brajeshwari D; Laitonjam,Warjeet S
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

65 .     (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:82.7%
Chinese Traditional and Herbal Drugs          2010          41          1065-1068
СҶÈ̶¬ÌٵĻ¯Ñ§³É·ÖÑо¿
Áõΰ;°×ËØƽ;Áº»á¾ê;Ô¬ÓÀÁÁ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

66 .     stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:82.7%
Chinese Traditional and Herbal Drugs          2008          39          1606-1609
Chemical constituents of Amtipathes dichotoma
SU Guo-chen; ZHANG Si; QI Shu-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

67 .     (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol
C28H46O3     ÏàËƶÈ:82.7%
Chinese Traditional and Herbal Drugs          1994          25          342-343+390
Studies on the Chemical Constituents of Kuhonggu (Russula rosacea)(¢ò)
Wang Huaibin; Xu Weishen; et al(Institute of Materia Medica; Chinese Academy of Medica Sciences; Beijing);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

68 .     (24R)-ergosta-7,22-diene-3,5,6-triol
    ÏàËƶÈ:82.7%
Chinese Journal of Natural Medicines          2008          6          348-353
Chemical Constituents of Marine Sponge Biemna fortis Topsent
HUANG Xiao-Chun; LIU Hai-Li; GUO Yue-Wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

69 .     3¦Â,5¦Á-Dihydroxy-6¦Â-methoxyergosta-7,22-diene
    ÏàËƶÈ:82.7%
Archives of Pharmacal Research          2002          25          851-855
Cytotoxic ergosterols from paecilomyces sp. J300
Hak Cheol Kwon, Sang Deuk Zee, Sae Yun Cho, Sang Un Choi and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

70 .     cerevisterol
    ÏàËƶÈ:82.7%
Archives of Pharmacal Research          2005          28          889-891
Antibacterial constituents from fruit bodies of Ascomyce Bulgaria inquinans
Peng Zhang, Xian Li, Ning Li, Jing Xu and Zhan-Lin Li, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

71 .     3¦Â,5¦Á-dihydroxy-6¦Â-methoxyergosta-7,22-diene
    ÏàËƶÈ:82.7%
Archives of Pharmacal Research          2006          29          548-555
Cytotoxic and COX-2 inhibitory constituents from the aerial parts ofAralia cordata
Ik Soo Lee, Wen Yi Jin, Xinfeng Zhang, Tran Manh Hung and Kyung Sik Song, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

72 .     Cerevisterol
    ÏàËƶÈ:82.7%
Archives of Pharmacal Research          2006          29          479-483
Constituents from the fruiting bodies of Ganoderma applanatum and their aldose reductase inhibitory activity
Sang Hyun Lee, Sang Hee Shim, Ju Sun Kim and Sam Sik Kang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

73 .     ergosta-7,22-diene-3,5,6-triol
C28H46O3     ÏàËƶÈ:82.7%
Chinese Pharmaceutical Journal          2003          38          499-5001
Studies on chemical constituents of Cordyceps sinensis(Berk) Sacc
LI Jie-xiu, LI Jin, XU Li-zhen, YANG Shi-lin, ZOU Zhong-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

74 .     ergosta-7,22-dien-2¦Â,3¦Á,9¦Á-triol
    ÏàËƶÈ:82.7%
Chinese Pharmaceutical Journal          2010          45          413-415
A New Sterol from the Fruiting Bodies of Ganoderma sinense Zhao, Xu et Zhang
LIU Chao, CHEN Ruo-yun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

75 .     22 E-ergosta-7,22-dien-3¦Â,5¦Â,6¦Â-triol
    ÏàËƶÈ:82.7%
Chinese Journal of Medicinal Chemistry          2006          16          98-101
The constituents of marine fungus 97F49
ZHANG Qing-hua, WANG Nai-li, GAO Hao, LIU Hong-wei, SONG Shan-shan, MICHIO Namikoshi, YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

76 .     (22E,24R)-ergos-ta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:82.7%
Journal of Shenyang Pharmaceutical University          2009          26          796-799
Isolation and identification of steroids from the leaves of theMagnolia sieboldii K. Koch
WANG Ru-ping, WU Di, GAO Hui-yuan, SUN Bo-hang, HUANG Jian, WU Li-jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

77 .     (22E,24R)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol
    ÏàËƶÈ:82.7%
Journal of China Pharmaceutical University          2007          38          315-319
Chemical constituents of the aerial parts of Euphorbia sororia
ZHANG Wei-ku; ZHANG Xiao-qi; YE Wen-cai;
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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78 .     24-Ethylcholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:82.7%
Bulletin of the Korean Chemical Society          2011          32          697-700
Isolation of Protein Tyrosine Phosphatase 1B Inhibitory Constituents from the Sclerotia of Polyporus umbellatus Fries
Hee Sang Lee, In Hyun Hwang, Jeong Ah Kim, Ji Young Choi, Tae Su Jang, Hiruyuki Osada, Jong Seog Ahn*, MinKyun Na*, Seung Ho Lee*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

79 .     24-Methylcholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËƶÈ:82.7%
Bulletin of the Korean Chemical Society          2011          32          697-700
Isolation of Protein Tyrosine Phosphatase 1B Inhibitory Constituents from the Sclerotia of Polyporus umbellatus Fries
Hee Sang Lee, In Hyun Hwang, Jeong Ah Kim, Ji Young Choi, Tae Su Jang, Hiruyuki Osada, Jong Seog Ahn*, MinKyun Na*, Seung Ho Lee*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

80 .     ergosta-7,11-dien-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËƶÈ:82.7%
Natural Product Research and Development          2010          22          235-237
Studies on the Chemical Constituents of Rhodobryum giganteum (schwaegr.) Par.
JIAO Wei; LU Gai-li; SHAO Hua-wu; LU Run-hua;
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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1 .     enniatin B
    ÏàËƶÈ:71.4%
Phytochemistry          2002          60          33-38
JM47, a cyclic tetrapeptide HC-toxin analogue from a marine Fusarium species
Zhong Jiang, Marc-Olivier Barret, Kenneth G. Boyd,David R. Adams, Alan S.F. Boyd, J. Grant Burgess
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     compound 9
C15H27NO5     ÏàËƶÈ:64.2%
The Journal of Antibiotics          2004          57          732-738
Enniatin Production by the Entomopathogenic Fungus Verticillium hemipterigenum BCC 1449
SUMALEE SUPOTHINA,MASAHIKO ISAKA,KANYAWIM KIRTIKARA,MORAKOT TANTICHAROEN and YODHATHAI THEBTARANONTH
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     enniatin B
    ÏàËƶÈ:64.2%
Australian Journal of Chemistry          2002          55          225-227
A Novel Compound Enniatin G from the Mangrove Fungus Halosarpheia sp. (strain #732) from the South China Sea
Y. Lin , J. Wang, X. Wu, S. Zhou, L. L. P. Vrijmoed and E. B. G. Jones
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     2-{[(1S,3R,4R,6R)-4-bromo-3,7,7-trimethylbicyclo[4.1.0]hept-3-yl]oxy}ethanol
    ÏàËƶÈ:57.1%
Helvetica Chimica Acta          2011          94          2188-2193
An Efficient Synthesis of Optically Active trans-(3R,4R)-3-Acetoxy-4-aryl-1-(chrysen-6-yl)azetidin-2-ones Using (+)-Car-3-ene as a Chiral Auxiliary (pages 2188¨C2193)
Aarif L. Shaikh, Orlando Esparza and Bimal K. Banik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     4-acetyl-1,7,7-trimethylbicyclo[2.2.1]hept-exo-2-yl acetate
    ÏàËƶÈ:57.1%
Russian Journal of Organic Chemistry          2010          46          1493-1502
Rearrangements and Hydration of 2-Ethynylisoborneol and 2-Ethynylisocamphanol
S. S. Koval¡¯skaya, N. G. Kozlov and E. A. Dikusar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     enniatin B
C33H57N3O9     ÏàËƶÈ:57.1%
Journal of Northwest A&F University (Natural Science)          2005          33          61-64
Identification of fungicidal compounds from endophytic fungi Fusarium proliferatum in celastrus angulatus
JI Zhi qin, WU Wen jun, WANG Ming an, GU Ai guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     Enniatin B
    ÏàËƶÈ:57.1%
Journal of Agricultural and Food Chemistry          1992          40          1076-1082
Production of enniatins by Fusarium acuminatum and Fusarium compactum in liquid culture: isolation and characterization of three new enniatins, B2, B3, and B4
Angelo. Visconti, Lisa A. Blais, John W. ApSimon, Roy. Greenhalgh, J. David. Miller
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     bucharioside
C16H28O7     ÏàËƶÈ:56.2%
Phytochemistry          1999          52          1319-1322
Bucharioside and buchariol from Salvia bucharica
Viqar Uddin Ahmad, Muhammad Zahid, Muhammad Shaiq Ali, Amir Reza Jassbi, Muhammad Abbas, Zul®qar Ali, Muhammad Zafar Iqbal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     L-O-Lac-L-Val-D-O-Hiv-D-Val
C18H32N2O7     ÏàËƶÈ:55.5%
Natural Product Communications          2012          7(2)          211-214
A New Peptide Isolated from a Marine Derived Streptomyces bacillaris
Youcai Hu and John B. MacMillan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     ent-cubeban-11-ol
C15H26O     ÏàËƶÈ:53.3%
Phytochemistry          2005          66          1662-1670
ent-Verticillane-type diterpenoids from the Japanese liverwort Jackiella javanica
Fumihiro Nagashima , Katsuhiro Kishi, Yuko Hamada,Shigeru Takaoka, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     (-)-sophoridine N-oxide
C15H24N2O2     ÏàËƶÈ:53.3%
Chemical & Pharmaceutical Bulletin          1980          28          546-551
The Alkaloid Constituents of Euchresta japonica and the Stereochemical Assignment of Two Isomeric Sophoridine N-Oxides
SHIGERU OHMIYA,HIROTAKA OTOMASU,JOJU HAGINIWA and ISAMU MURAKOSHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     4,10-epi-5¦Â-hydroxydihydroeudesmol
C15H28O2     ÏàËƶÈ:53.3%
Chemical & Pharmaceutical Bulletin          1987          35          1460-1463
Novel Eudesmane-Type Sesquiterpenes from Alpinia japonica (THUNB.) MIQ
HIDEJI ITOKAWA,HIROSHI MORITA and KINZO WATANABE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     10¦Î-hydroperoxy-¦Á-santal-11-ene
C15H24O2     ÏàËƶÈ:53.3%
Phytochemistry          1999          50          1213-1218
Santalane and isocampherenane sesquiterpenoids from Illicium tsangii
Koon-Sin Ngo, Geo}rey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     10¦Î-hydroxy-¦Á-santal-11-ene (¦Á-photosantolol B diastereoisomer)
    ÏàËƶÈ:53.3%
Phytochemistry          1999          50          1213-1218
Santalane and isocampherenane sesquiterpenoids from Illicium tsangii
Koon-Sin Ngo, Geo}rey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

15 .     10¦Î-hydroxy-¦Á-santal-11-ene (¦Á-photosantolol B diastereoisomer)
C15H24O     ÏàËƶÈ:53.3%
Phytochemistry          1999          50          1213-1218
Santalane and isocampherenane sesquiterpenoids from Illicium tsangii
Koon-Sin Ngo, Geo}rey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

16 .     compound 14
C15H26O     ÏàËƶÈ:53.3%
Phytochemistry          1997          46          1203-1208
Terpenoids from the Japanese liverworts Jackiella javanica and Jungermannia infusca
Fumihiro Nagashima, Akiko Tamada, Noriko Fujii, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

17 .     2-(Deca-6,9-diynyloxy)-tetrahydro-2H-pyran
C15H22O2     ÏàËƶÈ:53.3%
The Journal of Organic Chemistry          2011          76          4467-4481
Polyunsaturated Alkyl Amides from Echinacea: Synthesis of Diynes,Enynes, and Dienes
Nicholas J. Matovic, Patricia Y. Hayes, Kerry Penman, Reginald P. Lehmann,and James J. De Voss
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     eudesmandiol diastereomer
    ÏàËƶÈ:53.3%
Phytochemistry          1989          28          936-938
A eudesmanediol from Cymbopogon distans
C.S. Mathela,A.B. Melkani,Alka Pant,Vasu Dev,Thomas E. Nelson,Hakon Hope,Albert T. Bottini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

19 .     Compound 14
    ÏàËƶÈ:53.3%
Magnetic Resonance in Chemistry          2003          41          1034-1037
Complete NMR assignment of (+)-10¦Â, 14-dihydroxy-allo-aromadendrane
Lucin¨¦ia Vizzotto, Rozanna Marques Muzzi and D¨ºnis Pires de Lima
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

20 .     ¡÷13,14-iso-¦Á-santalol
C15H24O     ÏàËƶÈ:53.3%
Phytochemistry          1984          23          595-597
Sesquiterpenes from severinia buxifolia
Wu Tian-Shung, Masatake Niwa, Hiroshi Furukawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

21 .     (+)-vitrenol [(1R,6R,7S,10R)-vitr-4-en-14-ol]
C15H24O     ÏàËƶÈ:53.3%
Journal of the Chemical Society, Perkin Transactions 1          1984                   215-221
Structure and absolute configuration of (+)-vitrenal, a novel carbon skeletal sesquiterpenoid having plant-growth-inhibitory activity, from the liverwort Lepidozia vitrea
Akihiko Matsuo, Seiryo Uto, Hir¨­shi Nozaki and Mitsuru Nakayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

22 .     (1R,2R,4S)-trans-2-hydroxy-1,8-cineole ¦Â-D-glucopyranoside
C16H26O7     ÏàËƶÈ:53.3%
Bioscience, Biotechnology, and Biochemistry          2001          65          950-953
Isolation and Identification of trans-2- and trans-3-Hydroxy-1,8-cineole Glucosides from Alpinia galanga
Yuki SOMEYA, Akio KOBAYASHI, Kikue KUBOTA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

23 .     1-(tert-butyldimethylsilyloxy)-5,9-hexadecadiyne
    ÏàËƶÈ:52.9%
Journal of Natural Products          2002          65          1715-1718
Total Synthesis and Biological Evaluation of (5Z,9Z)-5,9-Hexadecadienoic Acid,an Inhibitor of Human Topoisomerase I
N¨¦stor M. Carballeira,Jos¨¦ E. Betancourt, Elsie A. Orellano, and Fernando A. Gonz¨¢lez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

24 .     chloropanaxydiol acetate
C21H29ClO5     ÏàËƶÈ:52.9%
Chemical & Pharmaceutical Bulletin          1988          36          4206-4208
A new Cytotoxic Chlorine-Containing Polyacetylene from the Callus of Panax ginseng
YASUO FUJIMOTO and MITSURU SATOH
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

25 .     Boc-Val-Vai-pNA
    ÏàËƶÈ:52.9%
Bioorganic & Medicinal Chemistry          1996          4          2201-2209
Use of BOP-Cl in the presence of Boc-amino monothioacids for the thioacylation of iminoacid residues
Hoang-Thanh Le, Jean-François Gallard, Michel Mayer, Eric Guittet, Robert Michelot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

26 .     antiprotealide
C12H18ClNO4     ÏàËƶÈ:50%
Journal of Natural Products          2009          72          295-297
Antiprotealide Is a Natural Product
Rama Rao Manam, Venkat R. Macherla, Ginger Tsueng, Chris W. Dring, Jeffrey Weiss, Saskia T. C. Neuteboom, Kin S. Lam, and Barbara C. Potts
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

27 .     Octyl ¦Â-D-Glucopyranoside
C14H28O6     ÏàËƶÈ:50%
Chemical & Pharmaceutical Bulletin          2001          49(4)          396-401
Prolyl Endopeptidase Inhibitors from the Underground Part of Rhodiola sachalinensis
Wenzhe FAN,Yasuhiro TEZUKA,Khin May NI,and Shigetoshi KADOTA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

28 .     petroside
C16H26O8     ÏàËƶÈ:50%
Chemical & Pharmaceutical Bulletin          2000          48(7)          1039-1044
Medicinal Foodstuffs. XVIII. Phytoestrogens from the Aerial Part of Petroselinum crispum MILL. (PARSLEY) and Structures of 6"-Acetylapiin and a New Monoterpene Glycoside, Petroside
Masayuki YOSHIKAWA,Toshiaki UEMURA,Hiroshi SHIMODA,Akinobu KISHI,Yuzo KAWAHARA and Hisashi MATSUDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

29 .     (+) (1R*, 2R*, 4R*)-trihydroxy-p-menth-3-ene
C10H20O3     ÏàËƶÈ:50%
Phytochemistry          2006          67          2103-2109
¦Á-Pinene-type monoterpenes and other constituents from Artemisia suksdorfii
Ahmed A. Mahmoud , Ahmed A. Ahmed
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

30 .     salinosporamide J
C15H20NO3Cl     ÏàËƶÈ:50%
Journal of Natural Products          2007          70          269-276
Salinosporamides D-J from the Marine Actinomycete Salinispora tropica, Bromosalinosporamide, and Thioester Derivatives Are Potent Inhibitors of the 20S Proteasome
Katherine A. Reed, Rama Rao Manam, Scott S. Mitchell, Jianlin Xu, Sy Teisan, Ta-Hsiang Chao, Gordafaried Deyanat-Yazdi,Saskia T. C. Neuteboom, Kin S. Lam, and Barbara C. M. Potts
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

31 .     1,5-dodecadiyne
    ÏàËƶÈ:50%
Journal of Natural Products          2002          65          1715-1718
Total Synthesis and Biological Evaluation of (5Z,9Z)-5,9-Hexadecadienoic Acid,an Inhibitor of Human Topoisomerase I
N¨¦stor M. Carballeira,Jos¨¦ E. Betancourt, Elsie A. Orellano, and Fernando A. Gonz¨¢lez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

32 .     5,9-hexadecadiyn-1-ol
    ÏàËƶÈ:50%
Journal of Natural Products          2002          65          1715-1718
Total Synthesis and Biological Evaluation of (5Z,9Z)-5,9-Hexadecadienoic Acid,an Inhibitor of Human Topoisomerase I
N¨¦stor M. Carballeira,Jos¨¦ E. Betancourt, Elsie A. Orellano, and Fernando A. Gonz¨¢lez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

33 .     5,9-hexadecadiynal
    ÏàËƶÈ:50%
Journal of Natural Products          2002          65          1715-1718
Total Synthesis and Biological Evaluation of (5Z,9Z)-5,9-Hexadecadienoic Acid,an Inhibitor of Human Topoisomerase I
N¨¦stor M. Carballeira,Jos¨¦ E. Betancourt, Elsie A. Orellano, and Fernando A. Gonz¨¢lez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

34 .     5,9-hexadecadiynoic Acid
    ÏàËƶÈ:50%
Journal of Natural Products          2002          65          1715-1718
Total Synthesis and Biological Evaluation of (5Z,9Z)-5,9-Hexadecadienoic Acid,an Inhibitor of Human Topoisomerase I
N¨¦stor M. Carballeira,Jos¨¦ E. Betancourt, Elsie A. Orellano, and Fernando A. Gonz¨¢lez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

35 .     valinoctin B
C14H28N2O4     ÏàËƶÈ:50%
Journal of Natural Products          1996          59          232-236
Isolation and Synthesis of Novel Farnesyl Protein Transferase Inhibitors, Valinoctins A and B, from Streptomyces Strain MJ858-NF3
Ryuichi Sekizawa, Hironobu Iinuma, Yasuhiko Muraoka, Hiroshi Naganawa, Naoko Kinoshita, Hikaru Nakamura, Masa Hamada, Tomio Takeuchi, and Kazuo Umezawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

36 .     (3¦Î,4¦Î)-3-isopropyl-3,4-epoxypentane-1,5-diol-1-O-¦Â-D-glucoside
C14H26O8     ÏàËƶÈ:50%
Chemical & Pharmaceutical Bulletin          1996          44          1797-1800
10-Carboxyloganin, Normonoterpenoid Gluosides and Dinormonoterpenoid Glucosides from the Leaves of Cerbera manghas(Studies on Cerbera. 10)
Fumiko ABE and Tatsuo YAMAUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

37 .     (-)-camoensidine N-oxide
C14H22N2O2     ÏàËƶÈ:50%
Chemical & Pharmaceutical Bulletin          1991          39          1123-1125
(-)-Camoensidine N-Oxide; A New Alkaloid from Maackia tashiroi
Shigeru OHMIYA,Hajime KUBO,Yuuichi NAKAAZE,Kazuki SAITO,Isamu MURAKOSHI and Hirotaka OTOMASU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

38 .     compound 6
    ÏàËƶÈ:50%
Chemical & Pharmaceutical Bulletin          1984          32          4833-4841
Studies on the Constituents of Leguminous Plants. VII. The Structure of Triterpenoid Saponins from Fruits of Gymnocladus chinensis BAILLON
TAKAO KONOSHIMA,TOKUNOSUKE SAWADA and TAKEATSU KIMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

39 .     (E)-(R)-2,6-dimethyl-8-hydroxyoct-2-enoic acid methyl ester 8-O-¦Â-D-glucopyranoside (6,7-dihydrofoliamenthoic acid methyl ester 8-O-¦Â-D-glucoside)
    ÏàËƶÈ:50%
Natural Product Research          2004          18          241-246
Glycosidic Monoterpenes from Linaria Capraria
Armandodoriano Bianco; Marcella Guiso; Mauro Ballero; Sebastiano Foddai; Marcello Nicoletti; Antonella Piccin; Mauro Serafini; Lamberto Tomassini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

40 .     beauvericin
C46H59N3O9     ÏàËƶÈ:50%
Journal of Natural Products          1995          Vol 58          733-738
Isolation of Novel Beauvericin Analogues from the Fungus Beauveria bassiana
Sandeep Gupta, Clytia Montllor, Yih-Shen Hwang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

41 .     epiheterodendrin
    ÏàËƶÈ:50%
Phytochemistry          1996          41          779-785
Leucine-derived nitrile glucosides in the rosaceae and their systematic significance
Matthias Lechtenberg, Adolf Nahrsted, Frank R. Fronczek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

42 .     (1S,4R,6R)-1,3,3-trimethyl-2-oxabicyclo[2.2.2]octan-6-O-¦Â-glucopyranoside[(1S,2R,4R)-1,8-epoxy-pmenthan-2-yl-O-¦Â-D-glucopyranoside
C16H28O7     ÏàËƶÈ:50%
Phytochemistry          1995          39          1115-1118
Linalool and cineole type glucosides from Cunila spicata
Detlef Manns
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

43 .     n-octyl ¦Â-glucoside
    ÏàËƶÈ:50%
Phytochemistry          1995          38          351-354
Antifungal terpenoids produced by cypress after infection by Diplodia pinea f. sp. Cupressi
Zion Madar, Hugo E. Gottlieb, Miriam Cojocaru, Joseph Riov, Zvi Solel, Abraham Sztejnberg
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

44 .     (10R,19R)-13,16-Diisopropyl-10,19-dimethyl-1,7-dioxo-14,15-diazacycloheneicosa-13,15-dien-2,6-dione
    ÏàËƶÈ:50%
Chemistry of Natural Compounds          2011          Vol. 47, No. 2          206-209
SYNTHESIS FROM l-MENTHOL OF OPTICALLY ACTIVE MACROHETEROCYCLES CONTAINING ESTER,AZINE, OR HYDRAZIDE GROUPS
G. Yu. Ishmuratov, G. R. Mingaleeva, O. O. Shakhanova,R. R. Muslukhov, E. M. Vyrypaev, and A. G. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

45 .     (11R,20R)-14,17-Diisopropyl-11,20-dimethyl-1,8-dioxo-15,16-diazacyclodocosa-14,17-dien-2,7-dione
    ÏàËƶÈ:50%
Chemistry of Natural Compounds          2011          Vol. 47, No. 2          206-209
SYNTHESIS FROM l-MENTHOL OF OPTICALLY ACTIVE MACROHETEROCYCLES CONTAINING ESTER,AZINE, OR HYDRAZIDE GROUPS
G. Yu. Ishmuratov, G. R. Mingaleeva, O. O. Shakhanova,R. R. Muslukhov, E. M. Vyrypaev, and A. G. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

46 .     (1aS,2S,4aR,4bS,5S)-2-Acetoxymethyl-5-tert-butoxy-4-oxo-pyrrolidino[1,2-b]isoxazolidino[4,5-c]tetrahydrofurane
C15H23NO6     ÏàËƶÈ:50%
Canadian Journal of Chemistry          2006          84          534-539
Synthesis of 8-homocastanospermine1
Konrad Pa niczek, Dariusz Socha, Margarita Jurczak, Jolanta Solecka, and Marek Chmielewski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

47 .     N-octyl-¦Â-valienamine (NOV)
    ÏàËƶÈ:50%
Bioorganic & Medicinal Chemistry Letters          2011          21          7189-7192
Transformation of quercitols into 4-methylenecyclohex-5-ene-1,2,3-triol derivatives, precursors for thechemical chaperones N-octyl-4-epi-¦Â-valienamine (NOEV) and N-octyl-¦Â-valienamine (NOV)
Shinichi Kuno, Atsushi Takahashi, Seiichiro Ogawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

48 .     Tagitinin C
    ÏàËƶÈ:50%
Bioorganic & Medicinal Chemistry Letters          2012          22          2954-2958
Sesquiterpene lactones from Tithonia diversifolia act as peroxisome proliferator-activated receptor agonists
Hsiang-Ru Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

49 .     ¦Ã-methyl-¦Ä-hydroxy pentanoic acid glucoside
C30H41N2O8     ÏàËƶÈ:50%
Chemical & Pharmaceutical Bulletin          2009          57          759-763
Five New Steroidal Glycosides from the Stems of Solanum sodomaeum
Masateru Ono, Yuuki Uenosono, Hideharu Umaoka, Yuki Shiono, Tsuyoshi Ikeda, Masafumi Okawa, Junei Kinjo, Hitoshi Yoshimitsu and Toshihiro Nohara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

50 .     compound 12c
    ÏàËƶÈ:50%
Tetrahedron Letters          2000          41          2633-2637
An efficient method for the synthesis of enantiopure 2,3-anti-propionate aldols involving a 3,5-syn- or anti-diol subunit through chiral borane-mediated enantioselective aldol reaction coupled with radical reduction
Syun-ichi Kiyooka, Kazi A. Shahid
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

51 .     4¦Â-hydroxy-1-menthyl acetate
    ÏàËƶÈ:50%
Phytochemistry          1988          27          3861-3869
Preparation of biologically active substances and animal and microbial metabolites from menthols,cineoles and kauranes
Yoshinori Asakawa,Reiko Matsuda,Motoo Tori,Toshihiro Hashimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

52 .     2,2-dimethoxycarbonyl-3-(tetrahydropyranyloxy)tetrahydrothiophene
C13H20O6S     ÏàËƶÈ:50%
Heterocycles          2008          76          1337-1360
Synthesis of 2'-Deoxy-4'-C-hydroxymethyl-4'-thioribonucleosides and Their 2', 3'-Dideoxy and 2', 3'-Didehydro-2', 3'-dideoxy Analogues
Junzo Nokami, Masayuki Mae, Satoshi Fukutake, Tomoyuki Ubuka, and Mitsuhiro Yamada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

53 .     Jasminoside K
C16H26O7     ÏàËƶÈ:50%
Helvetica Chimica Acta          2010          93          763-771
Monoterpenoids from the Fruit of Gardenia jasminoides
Yang Yu, Hao Gao, Yi Dai, Ying Wang, He-Ru Chen and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

54 .     Compound 7
    ÏàËƶÈ:50%
Magnetic Resonance in Chemistry          2003          41          1034-1037
Complete NMR assignment of (+)-10¦Â, 14-dihydroxy-allo-aromadendrane
Lucin¨¦ia Vizzotto, Rozanna Marques Muzzi and D¨ºnis Pires de Lima
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

55 .     compound 6
    ÏàËƶÈ:50%
Tetrahedron Letters          2002          43          1175-1177
Analysis of 2-deuterated isopentenyl alcohols by 1H NMR of chiral esters
Jos¨¦-Luis Giner, David Kiemle, Daniel J Zuniga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

56 .     macrosphelide H
    ÏàËƶÈ:50%
Journal of the Chemical Society, Perkin Transactions 1          2001                   3046-3053
Absolute stereostructures of cell-adhesion inhibitors, macrosphelides C, E¨CG and I, produced by a Periconia species separated from an Aplysia sea hare
Takeshi Yamada, Masashi Iritani, Mitsunobu Doi, Katsuhiko Minoura, Tadayoshi Ito and Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

57 .     7-aza-3,3,4-trimethyl-2-thiatricyclo[5.4.0.01,4]undecan-8-one
C12H19NOS     ÏàËƶÈ:50%
Heterocycles          2000          53          2781-2788
Photochemistry of N-3-Butenyl- and N-4-Pentenylglutarimides: Intramolecular Thietane Formation and the Fission of Thietane Ring
Kazuaki Oda,* Takeshi Ishioka, Yuichi Fukuzawa, Naozumi Nishizono, and Minoru Machida*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

58 .     MK1688
C36H63N3O9     ÏàËƶÈ:50%
Tetrahedron          2003          59          1015-1020
Unusual enniatins produced by the insect pathogenic fungus Verticillium hemipterigenum: isolation and studies on precursor-directed biosynthesis
Chongdee Nilanonta, Masahiko Isaka, Rachada Chanphen, Nuntawan Thong-orn, Morakot Tanticharoen, Yodhathai Thebtaranonth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

59 .     Boc-(S)-Me-Val-Gly-OEt
C15H28N2O5     ÏàËƶÈ:50%
Tetrahedron          2000          56          1759-1775
Total Synthesis and Revision of Absolute Stereochemistry of Antillatoxin, an Ichthyotoxic Cyclic Lipopeptide from Marine Cyanobacterium Lyngbya majuscula
Fumiaki Yokokawa, Hideyasu Fujiwara, Takayuki Shioiri
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

60 .     Ahda-Ala-Val
C18H35N3O5     ÏàËƶÈ:50%
Tetrahedron          2000          56          8643-8656
Microginins, Zinc Metalloproteases Inhibitors from the Cyanobacterium Microcystis aeruginosa
Keishi Ishida, Taku Kato, Masahiro Murakami, Masayuki Watanabe, Mariyo F. Watanabe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

61 .     (2S,3R)-and (2R,3S)-2,3-epoxytetradec-5-yn-1-ol
C14H24O2     ÏàËƶÈ:50%
The Journal of Organic Chemistry          1998          63          3925-3932
Absolute Structure and Total Synthesis of Lipogrammistin-A, a Lipophilic Ichthyotoxin of the Soapfish
Hiroyuki Onuki, Kei Ito, Yoshimasa Kobayashi, Nobuaki Matsumori, and Kazuo Tachibana, Nobuhiro Fusetani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

62 .     (3R,5S)-9-(tert-butyldimethylsilyloxy)-3,5,9-trimethyl-decan-1-ol
C19H42O2Si     ÏàËƶÈ:50%
Bioorganic & Medicinal Chemistry          2009          17          1747-1763
13-Methyl-substituted des-C,D analogs of (20S)-1¦Á,25-dihydroxy-2-methylene-19-norvitamin D3 (2MD): Synthesis and biological evaluation
Katarzyna Plonska-Ocypa, Rafal R. Sicinski, Lori A. Plum, Pawel Grzywacz, Jadwiga Frelek, Margaret Clagett-Dame, Hector F. DeLuca
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

63 .     (3S,5S)-9-(tert-butyldimethylsilyloxy)-3,5,9-trimethyl-dec-an-1-ol
C19H42O2Si     ÏàËƶÈ:50%
Bioorganic & Medicinal Chemistry          2009          17          1747-1763
13-Methyl-substituted des-C,D analogs of (20S)-1¦Á,25-dihydroxy-2-methylene-19-norvitamin D3 (2MD): Synthesis and biological evaluation
Katarzyna Plonska-Ocypa, Rafal R. Sicinski, Lori A. Plum, Pawel Grzywacz, Jadwiga Frelek, Margaret Clagett-Dame, Hector F. DeLuca
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

64 .     2-{[(1S,3R,4R,6R)-4-bromo-3,7,7-trimethylbicyclo[4.1.0]hept-3-yl]oxy}acetic acid
    ÏàËƶÈ:50%
Helvetica Chimica Acta          2011          94          2188-2193
An Efficient Synthesis of Optically Active trans-(3R,4R)-3-Acetoxy-4-aryl-1-(chrysen-6-yl)azetidin-2-ones Using (+)-Car-3-ene as a Chiral Auxiliary (pages 2188¨C2193)
Aarif L. Shaikh, Orlando Esparza and Bimal K. Banik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

65 .     (10R,19R)-13,16-diisopropyl-10,19-dimethyl-1,7-dioxa-14,15-diazacyclohenicosa-13,15-diene-2,6-dione
    ÏàËƶÈ:50%
Russian Journal of Organic Chemistry          2011          47          1416-1425
Synthesis of macrocyclic azino and dihydrazido diesters by consecutive [2 + 1]- and [1 + 1]-condensations
G. Yu. Ishmuratov, G. R. Mingaleeva, M. P. Yakovleva, O. O. Shakhanova and R. R. Muslukhov, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

66 .     (11R,20R)-14,17-diisopropyl-11,20-dimethyl-1,8-dioxa-15,16-diazacyclodocosa-14,17-diene-2,7-dione
    ÏàËƶÈ:50%
Russian Journal of Organic Chemistry          2011          47          1416-1425
Synthesis of macrocyclic azino and dihydrazido diesters by consecutive [2 + 1]- and [1 + 1]-condensations
G. Yu. Ishmuratov, G. R. Mingaleeva, M. P. Yakovleva, O. O. Shakhanova and R. R. Muslukhov, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

67 .     L-O-Lac-L-Val-D-O-Hiv-D-Val
C18H32N2O7     ÏàËƶÈ:50%
Natural Product Communications          2012          7(2)          211-214
A New Peptide Isolated from a Marine Derived Streptomyces bacillaris
Youcai Hu and John B. MacMillan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

68 .     beauvericin
C45H57N3O9     ÏàËƶÈ:50%
Zeitschrift f¨¹r Naturforschung C          2010          65          207-210
Nematicidal Activity of Beauvericin Produced by the Fungus Fusarium bulbicola
A. Shimada, S. Fujioka, H. Koshino, and Y. Kimura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

69 .     lateritin
C15H19NO3     ÏàËƶÈ:50%
The Journal of Antibiotics          1993          46          1782-1787
LATERITIN, A NEW INHIBITOR OF ACYL-CoA: CHOLESTEROL ACYLTRANSFERASE PRODUCED BY Gibberella lateritium IFO 7188
KEIJI HASUMI, CHIKARA SHINOHARA, TAKASHI IWANAGA, AKIRA ENDO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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70 .     compound 37
    ÏàËƶÈ:50%
European Journal of Organic Chemistry          2011                   7116-7132
Synthetic Strategies Directed Towards 5a-Carbahexopyranoses and Derivatives Based on 6-endo-trig Radical Cyclizations
Ana M. G¨®mez, Clara Uriel, Maria D. Company and J. Crist¨®bal L¨®pez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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71 .     (2R,3R,4aR,7S,12aS)-octahydro-2,3-dimethoxy-2,3,7-trimethyl-4aH-[1,4]dioxino[2,3-c]oxecin-5(7H)-one
C16H28O6     ÏàËƶÈ:50%
Australian Journal of Chemistry          2005          58          511-516
A Chemoenzymatic Total Synthesis of the Undecenolide (¨C)-Cladospolide C
Martin G. Banwell, David T. J. Loong and Anthony C. Willis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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72 .     (4aR,6S,8aS)-2,2-di-tert-butyl-6-propylhexahydropyrano[3,2-d][1,3,2]dioxasiline
C17H34O3Si     ÏàËƶÈ:50%
Tetrahedron          2012          68          8994-9003
Enantiodivergent synthesis of (+)- and (−-isolaurepan
Gonzalo Pazos, Manuel P¨¦rez, Zoila G¨¢ndara, Generosa G¨®mez, Yagamare Fall
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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73 .     tert-butyl (S)-3-methyl-1-((S)-4-methylpent-1-en-3-ylamino)-1-oxobutan-2-ylcarbamate
C16H30N2O3     ÏàËƶÈ:50%
Tetrahedron          2012          68          10114-10121
An efficient entry to highly substituted chiral 2-oxopiperazines from ¦Á-amino acids via iodocyclization
Amit Kumar Jana, Sanjit Kumar Das, Gautam Panda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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74 .     compound 79
C16H29NO3     ÏàËƶÈ:50%
Journal of Medicinal Chemistry          1992          35          4284-4296
Design and synthesis of novel FKBP inhibitors
James R. Hauske, Peter Dorff, Susan Julin, Joseph DiBrino, Robin Spencer, Rebecca Williams
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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75 .     beauvericin
    ÏàËƶÈ:50%
Chinese Pharmaceutical Journal          2013          48          17-21
Secondary Metabolites from Endophyte Fungus Fusariums sp. LC £­1
HU Xiao-lan, XU Wen-feng, LU Xuan, WU Xin, BAI Jiao, , PEI Yue-hu,
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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76 .     3-Ethyl-4-methylpentanol ¦Â-D-glucopyranose
C14H28O6     ÏàËƶÈ:50%
Journal of Natural Medicines          2011          65          212-216
Prenylated flavonoid glucoside and two aliphatic alcohol glycosides from the leaves of Euodia meliaefolia (Hance) Benth.
Yuka Koyama ,Miwako Yamamoto ,Katsuyoshi Matsunami ,Hideaki Otsuka ,Takakazu Shinzato ,Yoshio Takeda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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77 .     12-Bromododec-2-yne
C12H21Br     ÏàËƶÈ:50%
Tetrahedron          2012          68          7695-7700
An efficient route to the musk odorant (R,Z)-5-muscenone via base-metal-catalysis
Konrad Lehr, Alois F¨¹rstner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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78 .     Methyl [3¦Á,4a¦Â,5¦Â,8¦Â,8a¦Â]-5-(Octahydro-5,8-epoxy-1H-2-benzopyran-3-yl)-5-iodopentanoate
    ÏàËƶÈ:50%
Journal of Medicinal Chemistry          1986          29          2335-2347
9,11-Epoxy-9-homo-14-oxaprosta-5-enoic acid derivatives. Novel inhibitors of fatty acid cyclooxygenase
Steven E. Hall, Wen Ching Han, Martin F. Haslanger, Don N. Harris, Martin L. Ogletree
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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79 .     compound 30
    ÏàËƶÈ:50%
The Journal of Antibiotics          2012          65          541-549
Revisiting the enniatins: a review of their isolation, biosynthesis, structure determination and biological activities FREE
Arlene A Sy-Cordero, Cedric J Pearce and Nicholas H Oberlies
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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80 .     compound 31
    ÏàËƶÈ:50%
The Journal of Antibiotics          2012          65          541-549
Revisiting the enniatins: a review of their isolation, biosynthesis, structure determination and biological activities FREE
Arlene A Sy-Cordero, Cedric J Pearce and Nicholas H Oberlies
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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81 .     Ethyl 1-Azido-2-{[(tert-butyl)dimethylsilyl]oxy}cyclopentanepropanoate
C16H31N3O3Si     ÏàËƶÈ:50%
Helvetica Chimica Acta          2012          95          2502-2514
Formal Synthesis of (−-Cephalotaxine
Monica G. Gonçalves-Martin, Sarunas Sigmantas and Philippe Renaud
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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82 .     (4S)-4-isopropylcyclohex-1-enecarboxylic acid 4-O-¦Â-D-glucopyranoside
C16H26O8     ÏàËƶÈ:50%
Acta Pharmaceutica Sinica          2012          47          1179-1182
A new monoterpenoid glucoside from the twigs of Chamaecyparis obtusa var.breviramea f.crippsii
XU Jian; ZHANG Yu-mei; CHEN Ke-li; TAN Ning-hua; LIU Yi-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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83 .     (S)-3-Hex-1-ynylnon-4-yne-2,3-diol
C15H24O2     ÏàËƶÈ:50%
The Journal of Organic Chemistry          2012          77          8657-8668
Synthesis of Furan-3-carboxylic and 4-Methylene-4,5-dihydrofuran-3-carboxylic Esters by Direct Palladium Iodide Catalyzed Oxidative Carbonylation of 3-Yne-1,2-diol Derivatives
Bartolo Gabriele, Raffaella Mancuso, Vito Maltese, Lucia Veltri, and Giuseppe Salerno
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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1 .     (E)-3-(4-hydroxy-2-methoxy-phenyl)-propenoic acid 4-hydroxy-3-methoxyphenyl ester
C17H16O6     ÏàËƶÈ:77.7%
Chinese Journal of Natural Medicines          2009          7          351-353
A New Phenylpropionate Derivative from the Rhizomes of Hedysarum polybotrys
CHENG Fan; ZOU Kun; ZHU Shu; KATSUKO Komatsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     4 -(4''-hydroxyphenyl-3'''-methoxy)-2''-oxo-3''- butenyl-3-(4'-hydroxyphenyl)-propenoate
C20H18O6     ÏàËƶÈ:75%
Chemical & Pharmaceutical Bulletin          2007          55(6)          940-943
New Sesquiterpenes and Calebin Derivatives from Curcuma longa
YongChi ZENG,Feng QIU,Kyoko TAKAHASHI,JianMu LIANG,GeXia QU,and XinSheng YAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     4''-(4'''-hydroxyphenyl)-2''-oxo-3''-butenyl-3-(4'-hydroxyphenyl- 3'-methoxy)-propenoate
C20H18O6     ÏàËƶÈ:75%
Chemical & Pharmaceutical Bulletin          2007          55(6)          940-943
New Sesquiterpenes and Calebin Derivatives from Curcuma longa
YongChi ZENG,Feng QIU,Kyoko TAKAHASHI,JianMu LIANG,GeXia QU,and XinSheng YAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     p-hydroxyphenylethanol ferulate
    ÏàËƶÈ:72.2%
China Journal of Chinese Materia Medica          2009          34          1512-1516
Chemical constituents of fresh celery
ZHOU Kailan, WU Bing, ZHUANG Yulei, DING Liqin , LIU Zhihui, QIU Feng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     2-O-caffeoyl-3-O-isoferuloyltartaric acid
    ÏàËƶÈ:72.2%
Natural Product Communications          2012          7          1353-1356
Efficient Counter-current Chromatographic Isolation and Structural Identification of Two New Cinnamic Acids from Echinacea purpurea
Ying Lu, JiaYin Li, MiLu Li, Xia Hu, Jun Tan and Zhong Hua Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     °¢ÎºËá-¶ÔôÇ»ù±½ÒÒ´¼õ¥
    ÏàËƶÈ:72.2%
Chinese Traditional and Herbal Drugs          2012          43          1289-1292
Chemical constituents in Oenanthe javanica
ZHANG Jian; LI Sheng-hua; GU Rong-hui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     1-O-feruloyl-3-O-p-coumaroylglycerol
C22H22O8     ÏàËƶÈ:70%
Modern Chinese Medicine          2009          11(6)          9-11
Chemical Constituents from the Stems of Asparagus officinalis
Sun Zhouxuan, Huang Xuefeng, Kong Lingyi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     1-(3-Fluoro-phenyl)-1,2-dihydro-naphtho[1,2-e][1,3] oxazin-3-one
C18H12FNO2     ÏàËƶÈ:68.4%
Journal of Heterocyclic Chemistry          2012          49          589-595
Lewis Acid Catalyzed Synthesis of 1-Aryl-1,2-dihydro-naphtho[1,2-e][1,3]oxazin-3-ones under Solvent Free Conditions: A Mechanistic Approach
Mukul Sharma, Sunny Manohar and Diwan S. Rawat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     4'-carbomethoxy-2'-hydroxyphenyl ferulate
C18H16O7     ÏàËƶÈ:66.6%
Natural Product Research          2007          21          736-741
New cinnamic acid esters from Ocimum basilicum
Bina S. Siddiqui; Huma Aslam; Sabira Begum; Syed Tariq Ali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     3,6-di-O-[3-(4'-hydroxy-3'-methoxyphenyl)-2-pro-penoyl]-myo-inositol
C26H28O12     ÏàËƶÈ:66.6%
Bioorganic & Medicinal Chemistry Letters          2000          10          1439-1442
Synthesis of feruloyl-myo-inositols and their inhibitory effects on superoxide generation
Asao Hosoda, Eisaku Nomura, Akira Murakami, Koichi Koshimizu, Hajime Ohigashi, Kazuhiko Mizuno, Hisaji Taniguchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     Tribulusimide D
C18H17NO6     ÏàËƶÈ:66.6%
Archives of Pharmacal Research          2010          33          67-70
Tribuli fructus constituents protect against tacrine-induced cytotoxicity in HepG2 cells
Erisa Byun, Gil-Saeng Jeong, Ren-Bo An, Tae Sun Min and Youn-Chul Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     4-[(3',4'-Dihydroxycinnamoyl)-oxy]-methyl cinnamate
C19H16O6     ÏàËƶÈ:66.6%
Chemistry of Natural Compounds          2010          46          184-186
A new naphthoquinone and a new neolignan from Ligularia vellerea rhizomes
C. F. Wang, Y. Zhao, S. Y. Shi, J. P. Li and Z. Z. Zhang, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     Vanillin
    ÏàËƶÈ:66.6%
Tetrahedron Letters          2001          42          6531-6534
Isochromans from 2-(3',4'-dihydroxy)phenylethanol
Marcella Guiso, Carolina Marra, Claudia Cavarischia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     N3-(6-nitro-1,3-benzothiazol-2-yl)-2-[(3,4,5-trifluorophenyl)amino]-3-pyridine carboxamide
C19H10F3N5O3S     ÏàËƶÈ:66.6%
Bioorganic & Medicinal Chemistry          2011          19          7136-7150
2-Anilinonicotinyl linked 2-aminobenzothiazoles and [1,2,4]triazolo[1,5-b] [1,2,4]benzothiadiazine conjugates as potential mitochondrial apoptotic inducers
Ahmed Kamal, Y.V.V. Srikanth, M. Naseer Ahmed Khan, Md. Ashraf, M. Kashi Reddy, Farheen Sultana, Tandeep Kaur, Gousia Chashoo, Nitasha Suri, Irum Sehar, Zahoor A. Wani, Arpita Saxena, Parduman R. Sharma, Shashi Bhushan, Dilip M. Mondhe, Ajit K. Saxena
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     p-Hydroxyphenethyl trans-Ferulate
C18H18O5     ÏàËƶÈ:66.6%
Journal of Agricultural and Food Chemistry          2006          54          8417-8424
Isolation and Identification of Phase II Enzyme-Inducing Agents from Nonpolar Extracts of Green Onion (Allium spp.)
Hang Xiao and Kirk Parkin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     3-ôÇ»ù-4-¼×Ñõ»ù±½¼×Ëá
    ÏàËƶÈ:66.6%
China Journal of Chinese Materia Medica          2012          37          2092-2099
Non-anthraquinones constituents from the roots of Knoxia valerianoides
ZHAO Feng; WANG Sujuan; WU Xiuli; YU Yang; YUE Zhenggang; LIU Bo; LIN Sheng; ZHU Chenggen; YANG Yongchun; SHI Jiangong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     9,9¡ä-O-di-(Z)-feruloyl-(-)-secoisolariciresinol
C40H42O12     ÏàËƶÈ:65%
Journal of Natural Products          2008          71(6)          1016-1021
Dihydroagarofuranoid Sesquiterpenes, a Lignan Derivative, a Benzenoid,and Antitubercular Constituents from the Stem of Microtropis japonica
Jih-Jung Chen, Chang-Syun Yang, Chien-Fang Peng, Ih-Sheng Chen, and Chang-Ling Miaw
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     Compound 13
C22H18FNO5S     ÏàËƶÈ:65%
Bioorganic & Medicinal Chemistry Letters          2009          19          1481-1483
Synthesis of sulfonyl curcumin mimics exerting a vasodilatation effect on the basilar artery of rabbits
Chan Mug Ahn, Byong-Gon Park, Ho Bum Woo, Jungyeob Ham, Woon-Seob Shin, Seokjoon Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     2-Acetoxy-benzoic acid 2-[3-(4-hydroxy-3-methoxyphenyl)-acryloyloxy]-ethyl ester
C21H20O8     ÏàËƶÈ:65%
Archiv der Pharmazie          2010          343          215-221
Novel Conjugates of Aspirin with Phenolic Acid as Anti-inflammatory Agents Having Significantly Reduced Gastrointestinal Toxicity
Shan Jiang, Ning Ding, Wei Zhang, Yichun Zhang, Meiyu Geng and Yingxia Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     Cinnaretamine
C20H23NO6     ÏàËƶÈ:65%
Natural Product Research          2011          25          26-30
A new amide from the stems of Cinnamomum reticulatum Hay
Chung-Yi Chen; Hung-Chun Yeh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     1-O-feruloyl-3-O-p-coumaroylglycerol
    ÏàËƶÈ:65%
Chinese Traditional and Herbal Drugs          2012          43          1061-1064
Chemical constituents from Sparganii Rhizoma
LIANG Qiao-li; KONG Li-juan; WU Qi-nan; Duan Jin-ao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     clinopodic acid B
C19H18O8     ÏàËƶÈ:63.1%
Journal of Natural Products          2009          72          1379-1384
Matrix Metalloproteinase-2 Inhibitors from Clinopodium chinense var. parWiflorum
Toshihiro Murata,Kenroh Sasaki,Kumiko Sato, Fumihiko Yoshizaki, Haruna Yamada, Hiromichi Mutoh, Kaoru Umehara,Toshio Miyase,Tsutomu Warashina,Hiroaki Aoshima, Homare Tabata, and Kouichi Matsubara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     cimiracemate A
C19H18O7     ÏàËƶÈ:63.1%
Phytochemistry          2002          61          409-413
Cimiracemates A¨CD, phenylpropanoid esters from the rhizomes of Cimicifuga racemosa
Shao-Nong Chen, Daniel S. Fabricant, Zhi-Zhen Lu, Hongjie Zhang,Harry H.S. Fong, Norman R. Farnsworth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     3-methoxy-4-hrdroxyphenylpropyl caffeate
C19H20O6     ÏàËƶÈ:63.1%
Acta Pharmaceutica Sinica          2007          Vol 42          621-624
Chemical constituents of Ligularia duciformis
FU Kai-zhou; YU Neng-jiang; ZHANG Yang; ZHAO Yi-m
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     (-)-divanillyltetrahydrofuran ferulate
C30H32O8     ÏàËƶÈ:63.1%
Phytochemistry          1985          24          626-628
Lignan from calyces of Diospyros kaki
Shin Matsuura, Munekazu Iinuma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     2-Hydroxy-benzoic acid 2-[3-(4-hydroxy-3-methoxyphenyl)-acryloyloxy]-ethyl ester
C19H18O7     ÏàËƶÈ:63.1%
Archiv der Pharmazie          2010          343          215-221
Novel Conjugates of Aspirin with Phenolic Acid as Anti-inflammatory Agents Having Significantly Reduced Gastrointestinal Toxicity
Shan Jiang, Ning Ding, Wei Zhang, Yichun Zhang, Meiyu Geng and Yingxia Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     (E,E)-1-(Benzotriazol-1-yl)-4,4-dichloro-1-(4-fluorophenylimino)-3-(4-methoxyphenylamino)-2-nitro-but-2-ene
C23H18Cl2FN6O3     ÏàËƶÈ:63.1%
Zeitschrift f¨¹r Naturforschung B          2010          65          843-860
Chemistry of Polyhalogenated Nitrobutadienes, Part 9: Acyclic and Heterocyclic Nitroenamines and Nitroimines from 2-Nitroperchlorobuta-1,3-diene
V. A. Zapol'skii, J. C. Namyslo, M. Gjikaj, and D. E. Kaufmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     6-(3,4-dimethoxyphenyl)-1,2-dimethoxynaphthalene
    ÏàËƶÈ:63.1%
Bioorganic & Medicinal Chemistry          2010          18          5194-5201
New 2-arylnaphthalenediols and triol inhibitors of HIV-1 integrase¡ªDiscovery of a new polyhydroxylated antiviral agent
C¨¦dric Maurin, C¨¦dric Lion, Fabrice Bailly, Nadia Touati, Herv¨¦ Vezin, Gladys Mbemba, Jean François Mouscadet, Zeger Debyser, Myriam Witvrouw, Philippe Cotelle
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

29 .     6-(benzofuran-2-yl)-2-chloro-9-(4-methoxyphenylmeth-yl)-9H-purine
C21H15ClN4O2     ÏàËƶÈ:63.1%
Bioorganic & Medicinal Chemistry          2009          17          6512-6516
Synthesis, structure, and antimycobacterial activity of 6-[1(3H)-isobenzofuranylidenemethyl]purines and analogs
Morten Brændvang, Vebjørn Bakken, Lise-Lotte Gundersen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

30 .     Compound 17
    ÏàËƶÈ:61.9%
Bioorganic & Medicinal Chemistry Letters          2005          15          3782-3786
Synthesis of novel curcumin mimics with asymmetrical units and their anti-angiogenic activity
Ho Bum Woo, Woon-Seob Shin, Seokjoon Lee, Chan Mug Ahn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

31 .     furan-2-carboxylic acid {3-[3-(4-hydroxy-3-methoxy-phenyl)-acryloyl]-phenyl}-amide
C21H17NO5     ÏàËƶÈ:61.9%
Bioorganic & Medicinal Chemistry          2008          16          3608-3615
Synthesis of curcumin mimics with multidrug resistance reversal activities
Yumi Um, Sungsik Cho, Ho Bum Woo, Yong Kee Kim, Hanna Kim, Jungyeob Ham, Su-Nam Kim, Chan Mug Ahn, Seokjoon Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

32 .     2-O-caffeoyl-3-O-feruloyltartaric acid
    ÏàËƶÈ:61.9%
Natural Product Communications          2012          7          1353-1356
Efficient Counter-current Chromatographic Isolation and Structural Identification of Two New Cinnamic Acids from Echinacea purpurea
Ying Lu, JiaYin Li, MiLu Li, Xia Hu, Jun Tan and Zhong Hua Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

33 .     candenatenin A
C18H20O5     ÏàËƶÈ:61.1%
Journal of Natural Products          2009          72          1395-1398
Candenatenins A-F, Phenolic Compounds from the Heartwood of Dalbergia candenatensis
Sarot Cheenpracha, Chatchanok Karalai, Chanita Ponglimanont, and Akkharawit Kanjana-Opas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

34 .     4-hydroxy-3-methoxyphenyl ferulate
C17H16O6     ÏàËƶÈ:61.1%
Planta Medica          2005          71          680-682
Cytotoxicities of Xanthones and Cinnamate Esters from Hypericum hookerianum
Rujida Wilairat, Jiradej Manosroi , Aranya Manosroi,Anake Kijjoa,Maria São Jos¨¦ Nascimento ,Madalena Pinto ,Artur M. S. Silva ,Graham Eaton,Werner Herz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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35 .     messerschmidin
C18H14O7     ÏàËƶÈ:61.1%
Chinese Chemical Letters          1992          3          975-976
TWO NEW NEOLIGNANS FROM MESSERSCHMIDIA SIBIRCA L.SSP.
ZHI ZHONG SONG,ZI MIN LIU,ZHONG JIAN JIA AND QI XIU ZHU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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36 .     (E)-3'-hydroxy-4'-(1''-hydroxyethyl)-phenyl-4-methoxycinnamate
C18H18O5     ÏàËƶÈ:61.1%
Natural Product Research          2007          21          736-741
New cinnamic acid esters from Ocimum basilicum
Bina S. Siddiqui; Huma Aslam; Sabira Begum; Syed Tariq Ali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     nordehydrocyclodercitin
C18H10N3S     ÏàËƶÈ:61.1%
Natural Product Research          2007          21          782-786
Nordehydrocyclodercitin, a hexacyclic pyridoacridine alkaloid from the marine ascidian, Aplidium sp.
Madhavi S. Agrawal; Bruce F. Bowden
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     p-Hydroxycinnamyl p-coumarate coniferyl p-coumarate
    ÏàËƶÈ:61.1%
Phytochemistry          1996          43          1189-1194
p-coumaroylated syringyl units in maize lignin: Implications for ¦Â-ether cleavage by thioacidolysis
John H. Grabber, Stephane Quideau, John Ralph
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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39 .     tamariscina ester A
    ÏàËƶÈ:61.1%
Acta Pharmaceutica Sinica          2004          Vol 39          41-45
Isolation and structural identification of chemical constituents from Selaginella tamariscina (Beauv.)Spring
BI Yue feng; ZHENG Xiao ke; FENG Wei sheng; SHI She po
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     N-trans-feruloyl trramine
    ÏàËƶÈ:61.1%
Phytochemistry          1992          31          2869-2872
Alkaloids of Fumaria indica
Atta-ur-Rahman, M.Khalid Bhatti, Farzana Akhtar, M.Iqbal Choudhary
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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41 .     2-((2-Carboxy-4-fluorophenyl)amino)-3-methoxybenzoic acid
    ÏàËƶÈ:61.1%
Bioorganic & Medicinal Chemistry          2011          19          2190-2198
Radiosynthesis and in vivo evaluation of 1-[18F]fluoroelacridar as a positron emission tomography tracer for P-glycoprotein and breast cancer resistance protein
Bernd Dörner,Claudia Kuntner,Jens P. Bankstahl ,Thomas Wanek ,Marion Bankstahl ,Johann Stanek , Julia M¨¹llauer , Florian Bauer , Severin Mairinger,Wolfgang Löscher ,Donald W. Miller , Peter Chiba , Markus M¨¹ller, Thomas Erker , Oliver Langer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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42 .     (Z)-6-hydroxy-2-(3-methoxybenzylidene)benzofuran-3(2H)-one
C16H12O4     ÏàËƶÈ:61.1%
Bioorganic & Medicinal Chemistry Letters          2011          21          4520-4523
Synthesis of aurones and their inhibitory effects on nitric oxide and PGE2 productions in LPS-induced RAW 264.7 cells
Seo Young Shin, Min Cheol Shin, Ji-Sun Shin, Kyung-Tae Lee, Yong Sup Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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43 .     4',8-dihydroxy-3'-methoxy-7-methylisoflavone
C17H14O5     ÏàËƶÈ:61.1%
Chemical & Pharmaceutical Bulletin          2009          57          346-360
Synthesis of Various Kinds of Isoflavones, Isoflavanes, and Biphenyl-Ketones and Their 1,1-Diphenyl-2-picrylhydrazyl Radical-Scavenging Activities
Hideyuki Goto, Yoshiyasu Terao and Shuji Akai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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44 .     6,7-dihydroxy-4-(3,4-dihydroxyphenyl)-naphthalene-2-carboxylic acid
    ÏàËƶÈ:61.1%
Phytochemistry          1989          28          867-869
Isolation and synthesis of 6,7-dihydroxy-4-(3,4-dihydroxyphenyl)naphthalene-2-carboxylic acid from Pellia epiphylla
Markus Rischmann,R¨¹diger Mues,Hans Geiger,Hans Josef Laas,Theophil Eicher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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45 .     2-bromo-N-isoquinol-5-yl-4,5-dimethoxybenzamide
    ÏàËƶÈ:61.1%
Journal of Heterocyclic Chemistry          2006          43          1261-1265
Synthesis of benzo[c][1,8]phenanthrolin-6-one through cyclization of N-(isoquinol-5-yl)-2-bromo-benzamide derivatives
Soizic Prado,Sylvie Michel,François Tillequin and Michel Koch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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46 .     bis-(2-bromo-4,5-dimethoxybenzoyl)(isoquinolin-5-yl)azane
    ÏàËƶÈ:61.1%
Journal of Heterocyclic Chemistry          2006          43          1261-1265
Synthesis of benzo[c][1,8]phenanthrolin-6-one through cyclization of N-(isoquinol-5-yl)-2-bromo-benzamide derivatives
Soizic Prado,Sylvie Michel,François Tillequin and Michel Koch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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47 .     4-(2,3-dihydroxyphenyl)-4,5-dihydropyrrolo[1,2-a]quinoxaline
C17H14N2O2     ÏàËƶÈ:61.1%
Journal of Heterocyclic Chemistry          2001          38          671-674
A versatile synthesis of 4,5-dihydropyrrolo[1,2-a]quinoxalines
Rodrigo Abonia, Braulio Insuasty, Jairo Quiroga, Heinz Kolshorn and Herbert Meier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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48 .     3-(3,4-dimethoxyphenyl)-4-methyl-2H-chromen-2-one
C18H14O4     ÏàËƶÈ:61.1%
Bioorganic & Medicinal Chemistry Letters          2010          20          3889-3892
A novel synthesis of 3-aryl coumarins and evaluation of their antioxidant and lipoxygenase inhibitory activity
Marina Roussaki, Christos A. Kontogiorgis, Dimitra Hadjipavlou-Litina, Stylianos Hamilakis, Anastasia Detsi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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49 .     N-(4-methoxybenzoyl)-N'-(1-methylindolyl-3-methylene)-hydrazine
C18H17N3O2Br     ÏàËƶÈ:61.1%
Molecules          2010          15          2187-2202
Novel Indole-Based Analogs of Melatonin: Synthesis and in Vitro Antioxidant Activity Studies
Hanif Shirinzadeh, Burcu Eren, Hande Gurer-Orhan, Sibel Suzen and Seçkin Özden
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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50 .     Compound 3c
    ÏàËƶÈ:61.1%
Magnetic Resonance in Chemistry          2007          45          265-268
1H and 13C NMR spectral characterization of some novel 7H-1, 2, 4-triazolo[3, 4-b] [1, 3, 4] thiadiazine derivatives (pages 265¨C268)
Xinxiang Lei, Lixue Zhang, Anjiang Zhang, Xiaoxia Ye and Jing Xiong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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51 .     N-(¶ÔôÇ»ù±½ÒÒ»ù)°¢ÎºËáõ£°·
    ÏàËƶÈ:61.1%
Chinese Traditional and Herbal Drugs          2010          41          867-870
´óѪÌٵĻ¯Ñ§³É·ÖÑо¿(¢ò)
³ÂÖÇÏÉ;¸ßÎÄÔ¶;Áõá·ÁÕ;ÕÅÌú¾ü
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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52 .     rosmarinic acid
    ÏàËƶÈ:61.1%
Chinese Pharmaceutical Journal          2004          39          335-336
Studies on chemical constituents of phenolic acids in Rabdosia rubescens
ZHENG Xiao-ke, LI Qin, FENG Wei-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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53 .     2-[(4-Hydroxy-3-methoxyphenyl)methylene]6,7-dihydroxybenzofuran-3-one
C16H12O6     ÏàËƶÈ:61.1%
Bioscience, Biotechnology, and Biochemistry          2004          68          2183-2185
Synthesis and Antioxidative Activity of 3¡ä,4¡ä,6,7-Tetrahydroxyaurone, a Metabolite of Bidens frondosa
Somepalli VENKATESWARLU, Gopala K. PANCHAGNULA and Gottumukkala V. SUBBARAJU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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54 .     2-(2,2-diphenylvinyl)hydroquinone
    ÏàËƶÈ:61.1%
Heterocycles          2002          57          1049-1055
Synthesis of Coumaran-5-ols ¡ª New Model Compounds for Bioantioxidants
Uta Schädel and Wolf D. Habicher*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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55 .     6,7-dimethoxy-2-[2-(4-nitrophenyl)ethyl]-1,2,3,4-tetrahydroisoquinoline
C19H22N2O4     ÏàËƶÈ:61.1%
Bioorganic & Medicinal Chemistry          2009          17          2524-2535
Synthesis and biological evaluation of a small molecule library of 3rd generation multidrug resistance modulators
Werner Klinkhammer, Henrik M¨¹ller, Christoph Globisch, Ilza K. Pajeva, Michael Wiese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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56 .     3'-methoxy-aurone
    ÏàËƶÈ:61.1%
Bioorganic & Medicinal Chemistry          2009          17          8073-8085
Natural and synthetic 2'-hydroxy-chalcones and aurones: Synthesis, characterization and evaluation of the antioxidant and soybean lipoxygenase inhibitory activity
Anastasia Detsi, Maya Majdalani, Christos A. Kontogiorgis, Dimitra Hadjipavlou-Litina, Panagiotis Kefalas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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57 .     3-(4-methyl-4,5-dihydropyrrolo[1,2-a]quinoxalin-4-yl)phenol
C18H16N2O     ÏàËƶÈ:61.1%
European Journal of Organic Chemistry          2010                   4719-4731
AuI-Catalyzed Direct Hydroamination/Hydroarylation and Double Hydroamination of Terminal Alkynes
Nitin T. Patil, Pediredla G. V. V. Lakshmi and Vipender Singh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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58 .     3-(4-methyl-4,5-dihydropyrrolo[1,2-a]quinoxalin-4-yl)aniline
C18H17N3     ÏàËƶÈ:61.1%
European Journal of Organic Chemistry          2010                   4719-4731
AuI-Catalyzed Direct Hydroamination/Hydroarylation and Double Hydroamination of Terminal Alkynes
Nitin T. Patil, Pediredla G. V. V. Lakshmi and Vipender Singh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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59 .     (3-nitrophenyl)-(9H-pyrido[2,3-b]indol-4-yl)amine
C17H12N4O2     ÏàËƶÈ:61.1%
European Journal of Organic Chemistry          2010                   6665-6677
Synthesis of 2-, 3-, and 4-Substituted Pyrido[2,3-b]indoles by C¨CN, C¨CO, and C¨CC(sp) Bond Formation
C¨¦dric Schneider, David Goyard, David Gueyrard, Benoît Joseph and Peter G. Goekjian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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60 .     compound 38
    ÏàËƶÈ:61.1%
Organic Magnetic Resonance          1984          22          491-504
13C nuclear magnetic resonance of some derivatives of phenothiazines, pyridobenzothiazines and phenoxazines
Misa V. Jovanovic and Edward R. Biehl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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61 .     Rosmarinic acid
    ÏàËƶÈ:61.1%
Records of Natural Products          2011          5          12-21
Relationship Between Chemical Structure and Antioxidant Activity of Luteolin and Its Glycosides Isolated from Thymus sipyleus subsp. sipyleus var. sipyleus
Ufuk Özgen*, Ahmet Mavi, Zeynep Terzi, Cavit Kazaz, Ali Asçı, Yusuf Kaya and Hasan Seçen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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62 .     (E)-1-(3-azidophenyl)-3-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-one
    ÏàËƶÈ:61.1%
Bioorganic & Medicinal Chemistry Letters          2011          21          3573-3577
Synthesis of substituted triazolyl curcumin mimics that inhibit RANKL-induced osteoclastogenesis
Sang-Kyu Park, Sangtae Oh, Hye Kyoung Shin, Seong Hwan Kim, Jungyeob Ham, Jae-Seok Song, Seokjoon Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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63 .     3',4'-Dimethoxyaurone (Z)
C17H14O4     ÏàËƶÈ:61.1%
Journal of Agricultural and Food Chemistry          2007          55          700-705
Synthesis and Insect Antifeedant Activity of Aurones against Spodoptera litura Larvae
Masanori Morimoto, Hiromi Fukumoto, Toki Nozoe, Ai Hagiwara, and Koichiro Komai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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64 .     4'-Hydroxy-3'-methoxyaurone
C16H12O4     ÏàËƶÈ:61.1%
Journal of Agricultural and Food Chemistry          2007          55          700-705
Synthesis and Insect Antifeedant Activity of Aurones against Spodoptera litura Larvae
Masanori Morimoto, Hiromi Fukumoto, Toki Nozoe, Ai Hagiwara, and Koichiro Komai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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65 .     compound 6a
    ÏàËƶÈ:61.1%
Journal of Agricultural and Food Chemistry          1998          46          2911-2913
Facile Synthesis of 4-Hydroxycinnamyl p-Coumarates
Fachuang Lu and John Ralph
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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66 .     6-(2-furyl)indolo[1,2-c]quinazoline
C19H12N2O     ÏàËƶÈ:61.1%
Journal of the Brazilian Chemical Society          2010          21          897-904
Synthesis of Some New Mono, Bis-Indolo[1, 2-c]quinazolines: Evaluation of their Antimicrobial Studies
Rondla Rohini, P. Muralidhar Reddy, Kanne Shanker, Anren Hu and Vadde Ravinder
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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67 .     6,7-¶þ¼×Ñõ»ù-2-ÝÁÒÒËá
C13H12O4     ÏàËƶÈ:61.1%
Natural Product Research and Development          2012          24          1210-1213
Chemical Constituents in Herb of Incarvillea younghusbandii Sprague
SHEN Lan; JIANG Si-ping; ZHU Hua-jie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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68 .     (Z)-2-[5-(4-Methoxyphenyl)pyrazol-3-yl]-3-(pyrrol-2-yl) acrylonitrile
    ÏàËƶÈ:61.1%
Bioorganic & Medicinal Chemistry          1999          7          1425-1436
Synthesis of E- and Z-Pyrazolylacrylonitriles and their evaluation as novel antioxidants
Virinder S Parmar, Ajay Kumar, Ashok K Prasad, Sanjay K Singh, Naresh Kumar, Shubhasish Mukherjee, Hanumantharao G Raj, Sanjay Goel, William Errington, Mohindar S Puar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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69 .     laurolitsine
C18H19NO4     ÏàËƶÈ:61.1%
Journal of Tropical and Subtropical Botany          2000          8          324-328
²òƤÕÁºÍÔ²Ò¶²òƤÕÁÖеİ¢ÆÓ·ÈÉúÎï¼î³É·Ö
ÑÏСºì, κТÒå, лº£»Ô, Áõ÷·¼, ÕÅ·ïÏÉ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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70 .     populoside C
C23H26O10     ÏàËƶÈ:60.8%
Journal of Natural Products          2006          69          1370-1373
Phenolic Glycosides with Antioxidant Activity from the Stem Bark of Populus davidiana
XinFeng Zhang, Phuong Thien Thuong, Byung-Sun Min, Tran Minh Ngoc, Tran Manh Hung, Ik Soo Lee, MinKyun Na, Yeon-Hee Seong, Kyung-Sik Song, and KiHwan Bae
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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71 .     N,N'-[2,2'-(5,5'-dihydroxy-4,4'-bi-1H-indol-3,3'-yl)diethyl]-diferulamide
    ÏàËƶÈ:60%
Chemical & Pharmaceutical Bulletin          1997          45          1910-1914
Antioxidative Compounds Isolated from Safflower (Carthamus tinctorius L.) Oil Cake
Hui Li ZHANG,Akito NAGATSU,Toshihiro WATANABE,SAKAKIBARA and Harumi OKUYAMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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72 .     9,9'-O-diferuloyl-(-)-secoisolarciresinol
    ÏàËƶÈ:60%
Chemical & Pharmaceutical Bulletin          1995          43          1937-1942
Chemical Evaluation of Betula Species in Japan. I.Constituents of Betula ermanii
Hiroyuki FUCHINO,Tetsuya SATOH and Nobutoshi TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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73 .     demethoxycurcumin
    ÏàËƶÈ:60%
China Journal of Chinese Materia Medica          2009          34          2891-2894
Chemical constituents from Piper longum
LIU Wenfeng, JIANG Zhiyong, CHEN Jijun, ZHANG Xuemei, MA Yunbao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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74 .     dihydroconiferyl ferulate
C20H22O6     ÏàËƶÈ:60%
Phytochemistry          2000          53          1075-1078
Alkaloids and phenylpropanoids from Peganum nigellastrum
Zhong-Ze Ma, Yoshio Hano, Taro Nomura, Ying-Jie Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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75 .     (¡À)-9,9'-O-diferuloylsccoisolariciresinol
    ÏàËƶÈ:60%
Phytochemistry          1991          30          315-319
A butanolide and phenolics from Machilus thunbergii
Hiroyuki Karikome, Yoshihiro Mimaki, Yutaka Sashida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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76 .     Threo-(-)-¿ª»·ÒìÂäÒ¶ËÉÖ¬´¼¶þ°¢ÎºËáõ¥
C40H46NO12     ÏàËƶÈ:60%
Chemical Journal of Chinese Universities          2010          31          947-952
Total Synthesis of the Dilignan threo(-)Diferuloysecoisolariciresinol
XIA Ya-Mu, WANG Wei,YANG Feng-Ke, CHANG Liang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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77 .     9,9'-O-Di-(E)-feruloyl-(-)-secoisolariciresinol
C40H42O12     ÏàËƶÈ:60%
Natural Product Research          2011          Vol. 25, No. 13          1243-1249
Chemical constituents from the roots of Xanthium sibiricum
Suqin Kan, Guangying Chen, Changri Han, Zhong Chen, Xinming Song, Ming Ren and Hong Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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78 .     Cinnabutamine
C20H23NO6     ÏàËƶÈ:60%
Natural Product Communications          2011          Vol. 6, No. 9          1297-1298
Amides from the Stems of Cinnamomum burmannii
Zi-Ling Hong, Jin-Cherng Huang, Soong-Yu Kuo and Chung-Yi Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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79 .     threo-(¡À)-¿ª»·ÒìÂäÒ¶ËÉÖ¬´¼¶þ°¢ÎºËáõ¥
C40H42NO12     ÏàËƶÈ:60%
Acta Chimica Sinica          2010          31          947-952
Total Synthesis of the Dilignan threo-(¡À)-D iferuloysecoisolariciresinol
XIA Ya-Mu,WANG Wei,YANG Feng-Ke,CHANG L iang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

80 .     1'-O-¦Â-D-(3,4-dihydroxyphenyl)-ethyl-6'-O-vanilloyl-glucopyranoside
    ÏàËƶÈ:60%
Journal of Shenyang Pharmaceutical University          2011          28          116-119
Isolation and identification of chemical constituents from stems of Stauntonia brachyanthera Hand. - Mazz.
CHEN Chao, LI Zhen-xing, MENG Da-li, LI Ning, LI Xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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1 .     (E)-3-(4-hydroxy-2-methoxy-phenyl)-propenoic acid 4-hydro ...

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