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56.62, 98.64, 100.61, 109.18, 100.23, 114.51, 118.48, 118.64, 123.25, 133.91, 157.06, 157.79, 160.54, 163.30, 164.92, 189.67.
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PSA: ½ð±Ò+1, 3u 2014-04-21 15:52:03
fanqingfei: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2014-04-21 16:11:53
²éѯ½á¹û£º¹²²éµ½154¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     longicornuol B
C16H12O5     ÏàËÆ¶È:81.2%
Bulletin of the Korean Chemical Society          2010          31          3025-3026
A New Phenolic Compound from Dendrobium longicornu
Jiangmiao Hu*, Weiwei Fan, Lu Zhou, Youxing Zhao, Jun Zhou*
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     spinosan B
C17H14O5     ÏàËÆ¶È:64.7%
Journal of Natural Products          2006          69          261-264
Metabolites of the ¡°Smoke Tree¡±, Dalea spinosa, Potentiate Antibiotic Activity against Multidrug-Resistant Staphylococcus aureus
Gil Belofsky, Roberto Carreno, Kim Lewis, Anthony Ball, Gabriele Casadei, and George P. Tegos
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     compound 2d
C19H16O3S     ÏàËÆ¶È:58.8%
Tetrahedron Letters          2002          43          6113-6115
A convenient one-pot synthesis of 2-(alkylthio)isoflavones from deoxybenzoins using a phase transfer catalyst
Young-Woo Kim, Robert W Brueggemeier
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     7-methoxy-3',4'-methylenedioxyisoflavone
C17H12O5     ÏàËÆ¶È:56.2%
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     Ì¼Æ×Ä£Äâͼ
5 .     1,3,11a-Trihydroxy-9-(3,5,7-trihydroxy-4H-1-benzopyran-4-on-2-yl)-5a-[1,3,11a-trihydroxy-5a-(3,4-dihydroxyphenyl)-5,6,11-hexahydro-5,6,11-trioxanaphthacen-12-on-9-yl] -5,6,11 - hexahydro -5,6,11-trioxanaphthacen-12-one
    ÏàËÆ¶È:56.2%
Chemistry of Natural Compounds          2008          44          427-431
OLIGOMERIC OXIDATION PRODUCTS OF THE FLAVONOID QUERCETIN
E. M. Chervyakovsky, D. A. Bolibrukh,D. L. Kurovskii, A. A. Gilep, T. M. Vlasova,V. P. Kurchenko, and S. A. Usanov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     coccineone B(75Hz)
    ÏàËÆ¶È:56.2%
Chinese Chemical Letters          2005          16          20-22
Synthesis of 6, 9, 11-Trihydroxy-6a, 12a-dehydrorotenoid
Hong Yan ZHENG, Shao Bai LI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     coccineone B(100Hz)
    ÏàËÆ¶È:56.2%
Chinese Chemical Letters          2005          16          20-22
Synthesis of 6, 9, 11-Trihydroxy-6a, 12a-dehydrorotenoid
Hong Yan ZHENG, Shao Bai LI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     3-Deoxysappanchalcone
C16H14O4     ÏàËÆ¶È:56.2%
Molecules          2008          13          1923-1930
A New 3-Benzylchroman Derivative from Sappan Lignum (Caesalpinia sappan)
Lin-chun Fu, Xin-an Huang, Zhen-yuan Lai, Ying-jie Hu, Hong-jiao Liu and Xiao-ling Cai
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     1,3-dihydroxy-5,6-dimethoxyxanthone
C15H12O6     ÏàËÆ¶È:56.2%
Journal of Natural Products          1988          Vol 51          339
Synthesis of 1,3-Dihydroxy-5,6-Dimethoxyxanthone, a Confirmation of Structure
S. Gil, M. Parra, V. Sanz, A. Tortajada
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     lupinalbin A
    ÏàËÆ¶È:56.2%
Acta Pharmaceutica Sinica          2008          Vol 43          67-70
Chemical constituents from Spatholobus sinensis
YIN Ting; LIU Hua; WANG Bin; TU Guang-zhong; LIANG Hong; ZHAO Yu-ying
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     5,2',5'-Trihydroxy-7-methoxyflavone
C16H12O6     ÏàËÆ¶È:56.2%
Journal of Asian Natural Products Research          2011          Vol.13,No.8          707-713
Neuropective constituents from the rhizomes of Abacopteris penangiana
Han Wei, Guang-Hua Wu, Yong-Fang Lei, Chao-Mei Xiong and Jin-Lan Ruan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     Lupinalbin A
C15H8O6     ÏàËÆ¶È:56.2%
Tetrahedron          2011          67          8654-8658
Total synthesis of the pyranocoumaronochromone lupinalbin H
Mamoalosi A. Selepe, Siegfried E. Drewes, Fanie R. van Heerden
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     2-Methoxy-4,5,7-trihydroxy-anthraquinone
    ÏàËÆ¶È:56.2%
Pharmazie          2000          55          785-786
2-Methoxy-4,5,7-trihydroxy-anthraquinone, a new lichen metabolite produced by Xanthoria parietina
V. Ivanova - R. Schlegel - U. Gräfe
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     compound 4g
C14H12FNO3     ÏàËÆ¶È:56.2%
Archiv der Pharmazie          2003          336          53-71
Relationship between the Structure and Antimycobacterial Activity of Substituted Salicylanilides
Karel Waisser, Otakar Bureš, Pavel Holy, Jiř¨ª Kuneš, Radek Oswald, Lucie Jir¨¢skov¨¢, Milan Pour, V¨§ra Klimešov¨¢, Lenka Kubicov¨¢ and Jarmila Kaustov¨¢
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     5-Hydroxy-3-(4-methoxyphenyl)-4-oxo-4H-chromen-7-yl 2-bromooacetate
C18H13BrO6     ÏàËÆ¶È:56.2%
Bioorganic & Medicinal Chemistry          2012          20          2962-2970
Ester and carbamate ester derivatives of Biochanin A: Synthesis and in vitro evaluation of estrogenic and antiproliferative activities
Nikolas Fokialakis, Xanthippi Alexi, Nektarios Aligiannis, Despina Siriani, Aggeliki K. Meligova, Harris Pratsinis, Sofia Mitakou, Michael N. Alexis
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2014-04-21 14:59:22
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