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55.22,59.74,103.34,114.36,115.09,115.84,118.18,120.38,122.70,125.70,130.32,132.61,143.73,144.02,144.51,144.69,153.56
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liangtingmei: ½ð±Ò+10 2015-06-01 18:53:20
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1 .     Neotaiwanensol B
C18H18O4     ÏàËÆ¶È:61.1%
Phytochemistry          2013          93          203-209
Neolignans and phenylpropanoids from the roots of Piper taiwanense and their antiplatelet and antitubercular activities
Si Chen, Hung-Yi Huang, Ming-Jen Cheng, Chin-Chung Wu, Tsutomu Ishikawa, Chien-Fang Peng, Hsun-Shou Chang, Chyi-Jia Wang, Su-Ling Wong, Ih-Sheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     6-(2,3-dibromo-4,5-dihydroxybenzyl)-2,3-dibromo-4,5-dihydroxy benzyl methyl ether
C15H14Br2O6     ÏàËÆ¶È:58.8%
Journal of Natural Products          2004          67          1661-1666
Dibenzyl Bromophenols with Diverse Dimerization Patterns from the Brown Alga Leathesia nana
Xiuli Xu, Fuhang Song, Sujuan Wang, Shuai Li, Fan Xiao, Jielu Zhao, Yongchun Yang, Suqing Shang, L Yang, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     rooperol
    ÏàËÆ¶È:58.8%
Phytochemistry          1989          28          153-156
Structure determination of a phenolic pent-1-en-4-yne derivative from Hypoxis rooperi
Siegfried E. Drewes,Ursula J. Scogings,George L. Wenteler
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     isomelacacidin
    ÏàËÆ¶È:58.8%
Phytochemistry          1986          25          1961-1965
Diastereoisomeric leucoanthocyanidins from the heartwood of acacia melanoxylon
Lai Yeap Foo, Herbert Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 5
C17H14O4     ÏàËÆ¶È:58.8%
Tetrahedron          1982          38          1683-1687
Research on African medicinal plants¡ªII: Hypoxoside, a new glycoside of uncommon structure from hypoxis obtusa busch
G.B.Marini Bettolo, M. Patamia, M. Nicoletti, C. Galeffi, I. Messana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     variegatic acid
C18H12O9     ÏàËÆ¶È:55.5%
Bioscience, Biotechnology, and Biochemistry          2009          73          855-860
In Vitro Inhibitory Effects of Pulvinic Acid Derivatives Isolated from Chinese Edible Mushrooms, Boletus calopus and Suillus bovinus, on Cytochrome P450 Activity
Yu-Ting HUANG, Jun-ichi ONOSE, Naoki ABE and Kunie YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     xerocomic acid
C18H12O8     ÏàËÆ¶È:55.5%
Bioscience, Biotechnology, and Biochemistry          2009          73          855-860
In Vitro Inhibitory Effects of Pulvinic Acid Derivatives Isolated from Chinese Edible Mushrooms, Boletus calopus and Suillus bovinus, on Cytochrome P450 Activity
Yu-Ting HUANG, Jun-ichi ONOSE, Naoki ABE and Kunie YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     terphenyllin
    ÏàËÆ¶È:55%
Natural Product Communications          2012          7          1057-1062
Two New p-Terphenyl Derivatives from the Marine Fungal Strain Aspergillus sp. AF119
Shao-Song Liu, Bao-Bing Zhao, Chun-Hua Lu, Jing-Jing Huang and Yue-Mao Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     2-(3-bromo-5-hydroxy-4-methoxyphenyl)-3-(2,3-dibromo-4,5-dihydroxyphenyl)propionic acid methyl ester
    ÏàËÆ¶È:52.9%
Journal of Natural Products          2004          67          1032-1035
Bromophenol Derivatives from the Red Alga Rhodomela confervoides
Jielu Zhao, Xiao Fan, Sujuan Wang, Shuai Li, Suqin Shang, Yongchun Yang, Nianjun Xu, Yang L, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     4'-methoxy-2'',3',3''-tribromo-4'',5',5''-trihydroxydiphenylacetic acid
C15H11O6Br3     ÏàËÆ¶È:52.9%
Journal of Natural Products          2004          67          1032-1035
Bromophenol Derivatives from the Red Alga Rhodomela confervoides
Jielu Zhao, Xiao Fan, Sujuan Wang, Shuai Li, Suqin Shang, Yongchun Yang, Nianjun Xu, Yang L, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     6-(2,3,6-tribromo-4,5-dihydroxybenzyl)-2,5-dibromo-3,4-dihydroxybenzyl methyl ether
C15H11Br5O5     ÏàËÆ¶È:52.9%
Journal of Natural Products          2007          70          1210-1213
Highly Brominated Mono- and Bis-phenols from the Marine Red Alga Symphyocladia latiuscula with Radical-Scavenging Activity
Xiao-Juan Duan,Xiao-Ming Li,and Bin-Gui Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     3,6-dihydroxy-5-methoxy-7-phenyl-3H-benzo[de]isochromene-1-one
C19H12O5     ÏàËÆ¶È:52.9%
Journal of Natural Products          2002          65          1122-1130
Phenylphenalenone-Related Compounds: Chemotaxonomic Markers of the Haemodoraceae from Xiphidium caeruleum
Stefan Opitz, Dirk Hölscher, Neil J. Oldham, Stefan Bartram, and Bernd Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     4-methoxy-9,10-dihydrophenanthrene-2,3,6,7-tetrol
C15H14O5     ÏàËÆ¶È:52.9%
Phytochemistry          1999          50          1237-1241
Phenanthrene and other aromatic constituents of Bulbophyllum vaginatum
Yuan-Wah Leong¦Á,Leslie J. Harrison¦Á, Andrew D. Powell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     2,2',3-tribromo-3',4,4',5-tetrahydroxy-6'-hydroxymethyldiphenylmethane
    ÏàËÆ¶È:52.9%
Chinese Journal of Marine Drugs          2003          22(2)          1-4,10
Studies on the chemical constituents of the marine alga Rhodomela confervoides
XU Nian-jun, FAN Xiao, SHI Jian-gong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     7,3',4'-Trihydroxy-3-benzyl-2H-chromene
C16H14O4     ÏàËÆ¶È:52.9%
Journal of Natural Medicines          2008          62          325-327
A new homoisoflavan from Caesalpinia sappan
Huanxin Zhao, Hong Bai, Yuanshu Wang, Wei Li and Kazuo Koike
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     2,3,3'-tribromo-4,4',5,5'-tetrahydroxyl-1'-ethyloxymethyldiphenyl methane
    ÏàËÆ¶È:52.9%
Chinese Traditional and Herbal Drugs          2007          38          652-655
Cytotoxic constituents from red alga Gymnogongrus flabelliformis
YUAN Zhao-hui; HAN Li-jun; FAN Xiao; LI Shuai; SHI Da-yong; SUN Jie; YANG Yong-chun; SHI Jian-gong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     3-bromo-4-(2,3-dibromo-4,5-dihydroxybenzyl)-5-methoxymethylpyrocatechol
    ÏàËÆ¶È:52.9%
Chinese Traditional and Herbal Drugs          2006          37          1462-1465
Chemical constituents from Polysiphonia urceolata
LIU Quan-wen; LI Gui-hua; LIU Ke; ZHANG Ting; FAN Xiao; GUO Hong-yan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     rosmarinic acid
    ÏàËÆ¶È:52.9%
Chinese Journal of Natural Medicines          2007          5          27-30
Water-Soluble Constituents of Clerodendranthus spicatus
WANG Min; LIANG Jing-Yu; CHEN Xue-Ying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     3,4,3',4'-tetrahydroxy-chalcone
    ÏàËÆ¶È:52.9%
Food Chemistry          2011          126          241-248
Hydroxychalcones as potent antioxidants: Structure¨Cactivity relationship analysis and mechanism considerations
Yi-Ping Qian, Ya-Jing Shang, Qing-Feng Teng, Jin Chang, Gui-Juan Fan, Xia Wei, Ran-Ran Li, Hong-Ping Li, Xiao-Jun Yao, Fang Dai, Bo Zhou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     hypoxoside
    ÏàËÆ¶È:52.9%
Food Chemistry          2007          101          1425-1437
Isolation, characterization and antioxidant capacity assessment of the bioactive compounds derived from Hypoxis rooperi corm extract (African potato)
Olga Laporta, Laura P¨¦rez-Fons, Ricardo Mallavia, Nuria Caturla, Vicente Micol
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     3-amino-N'-[1-(2,5-dimethoxyphenyl)ethylidene)-5,6-dihydro-4H-cyclopenta-thiophene-2-carbohydrazide
C18H21N3O3S     ÏàËÆ¶È:52.9%
Archives of Pharmacal Research          2012          35          965-973
Antitumor activity of novel pyridine, thiophene and thiazole derivatives
Mostafa M. Ghorab and Mansour S. Al-Said
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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