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1 . 6,7,2',4',5'-pentamethoxyisoflavone
C20H20O7 ÏàËÆ¶È:52.3%
Journal of Natural Products 2003 66 210-216
Six New Isoflavones and a 5-Deoxyflavonol Glycoside from the Leaves of Ateleia herbert-smithii
Nigel C. Veitch, Polly S. E. Sutton, Geoffrey C. Kite, and Helen E. Ireland
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
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2 . tatarinoid C
C21H28O7 ÏàËÆ¶È:52.3%
Journal of Natural Products 2010 73 1160-1163
Compounds from Acorus tatarinowii: Determination of Absolute Configuration by Quantum Computations and cAMP Regulation Activity
Xiao-Gang Tong, Gui-Sheng Wu, Cheng-Gang Huang, Qing Lu, Yue-Hu Wang, Chun-Lin Long, Huai-Rong Luo, Hua-Jie Zhu and Yong-Xian Cheng
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
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3 . O-methylpallidine N-oxide
ÏàËÆ¶È:52.3%
Journal of Natural Products 1989 Vol 52 415
O-Methylpallidine N-oxide, the First Morphinandienone N-oxide Alkaloid
Emilia Tojo, Domingo Dominguez, Luis Castedo
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
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4 . (+)-O-methylpallidine N-oxide
C20H23NO5 ÏàËÆ¶È:52.3%
Phytochemistry 1991 30 1005-1010
Alkaloids from Sarcocapnos enneaphylla
Emilia Tojo, Domingo Dominguez, Luis Castedo
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
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5 . 6,2',4',5'-tetramethoxy-7-hydroxyisoflavone
ÏàËÆ¶È:52.3%
Natural Product Communications 2010 5 903-906
Bioactive Isoflavones from Dalbergia vacciniifolia (Fabaceae)
Ester Innocent* Joseph J. Magadula, Charles Kihampa and Matthias Heydenreich
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
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6 . (E)-5,5'-(2-¼×»ùÎì-1-Ï©-1,3-¶þ»ù)¶þ(1,2,4-Èý¼×Ñõ»ù±½)
C24H32O6 ÏàËÆ¶È:52.1%
Chinese Journal of Organic Chemistry 2013 33 1982-1987
Acid-Catalyzed Dimerization of ¦Á-Asarone and Anticancer Evaluation of the Dimers
Xu Yingying, Liang Zhiwu, Liu Kaijian, Chen Hui, Xiang Jiannan
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
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7 . cis-1-(2,4,5-trimethoxy-E-styryl)-2-(2,4,5-trimethoxy-Z-styryl)cyclobutane
C26H32O6 ÏàËÆ¶È:50%
Phytochemistry 2001 56 109-114
Phenylbutanoid dimers from the leaves of Alpinia ¯abellata
Hiroe Kikuzaki a, Shoko Tesaki a, Sigetomo Yonemori b, Nobuji Nakatani
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
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8 . pachypostaudin-A
C22H28O6 ÏàËÆ¶È:50%
Phytochemistry 1989 28 231-234
Pachypophyllin and pachypostaudins A and B: three bisnorlignans from pachypodanthium staudtii
Bonaventure T. Ngadjui,David Lontsi,Johnson Foyere Ayafor,B.Lucas Sondengam
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
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9 . compound 14g
C24H25FO6S ÏàËÆ¶È:50%
European Journal of Organic Chemistry 2010 1798-1808
Regioselective Arylations of ¦Á-Amido Sulfones with Electron-Rich Arenes through Friedel¨CCrafts Alkylations Catalyzed by Ferric Chloride Hexahydrate: Synthesis of Unsymmetrical and Bis-Symmetrical Triarylmethanes
Ponnaboina Thirupathi and Sung Soo Kim
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
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10 . millesianin I
C24H26O7 ÏàËÆ¶È:50%
Fitoterapia 2014 95 154-159
Bioactivity-guided isolation of anti-inflammation flavonoids from the stems of Millettia dielsiana Harms
Haoyu Ye, Wenshuang Wu, Zhuowei Liu, Caifeng Xie, Minghai Tang, Shucai Li, Jianhong Yang, Huan Tang, Kai Chen, Chaofeng Long, Aihua Peng, Yuquam Wei, Lijuan Chen
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ
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11 . compound 1h
ÏàËÆ¶È:50%
Organic Magnetic Resonance 1976 8 324-326
Isobenzopyryliumsalts: VII¡ª13C n.m.r. shifts of 1-arylisobenzopyrylium salts and correlation with Hammett parameters
Miklos Vajda and Wolfgang Voelter
Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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