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13C NMR (126 MHz, MeOD) ¦Ä
7.39,25.63,93.69,103.94,105.49,107.92,108.78,117.20,123.44,132.27,155.08,157.21,157.67,158.37,160.12,163.98,183.17
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xieliting: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-06-05 16:51:11
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1 .     ophiopogonone D
C17H14O6     ÏàËÆ¶È:82.3%
Journal of Asian Natural Products Research          2009          11          876-879
Two new homoisoflavonoids from the fibrous roots of Ophiopogon japonicus (Thunb.) Ker-Gawl
Chang-Ling Duanac, Zhi-Yun Kangb, Cheng-Ren Linc, Yong Jianga, Jian-Xun Liuc and Peng-Fei Tu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     2'-hydroxygenistein
C15H10O6     ÏàËÆ¶È:82.3%
BMC Complementary and Alternative Medicine          2014          14          294
Lupinalbin A as the most potent estrogen receptor¦Á- and aryl hydrocarbon receptor agonist inEriosema laurentii de Wild. (Leguminosae)
Sylvin Benjamin Ateba, Dieudonn¨¦ Njamen, Svjetlana Medjakovic, Martin Zehl, Hanspeter Kaehlig, Alois Jungbauer and Liselotte Krenn
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     1,7-dihydroxy-2-methyl-3-methoxy-dibenz[b,f][1,4]oxaze-pin-11-(10H)-one
C15H13NO5     ÏàËÆ¶È:76.4%
Bioorganic & Medicinal Chemistry Letters          2007          17          636-639
Natural dibenzoxazepinones from leaves of Carex distachya: Structural elucidation and radical scavenging activity
Antonio Fiorentino, Brigida D¡¯Abrosca, Severina Pacifico, Giuseppe Cefarelli, Piera Uzzo, Pietro Monaco
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     orobol
C15H10O6     ÏàËÆ¶È:76.4%
Chinese Traditional and Herbal Drugs          2009          40          179-182
Chemical constituents in roots of Flemingia macrophylla
LI Bao-qiang; SONG Qi-shi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     5,7,3',4'-ËÄôÇ»ùÒì»ÆÍª
C15H10O6     ÏàËÆ¶È:76.4%
Chinese Traditional and Herbal Drugs          2009          40          865-868
Ðâëǧ½ï°Î¸ùµÄ»¯Ñ§³É·ÖÑо¿
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Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     2-(2'-methoxy,4'-hydroxy)-aryl-3-methyl-6-hydroxy-benzofuran
C16H14O4     ÏàËÆ¶È:76.4%
Fitoterapia          2013          85          35-40
Three new phenolic compounds from the roots of Glycyrrhiza yunnanensis
Qing Wang, Shuai Ji, Si-wang Yu, Hui-xia Wang, Xiong-hao Lin, Tao-tao Ma, Xue Qiao, Cheng Xiang, Min Ye, De-an Guo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     eriophorin B
C18H16O6     ÏàËÆ¶È:72.2%
Journal of Natural Products          2005          68          1094-1098
Flavonoids from the Stem of Eriophorum scheuchzeri
Milena Maver, Emerson F. Queiroz, Jean-Luc Wolfender, and Kurt Hostettmann
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     hydroxyderrone
    ÏàËÆ¶È:72.2%
Helvetica Chimica Acta          2015          98          561−568
Two New Flavonoids from Retama raetam
Wen-Hui Xu, Adnan J. Al-Rehaily, Muhammad Yousaf, Mohammad S. Ahmad, Shabana I. Khan and Ikhlas A. Khan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     7,2 ,4 -trihydroxy-5-methoxy-3-arylcoumarin
C16H12O6     ÏàËÆ¶È:70.5%
Chemical & Pharmaceutical Bulletin          2008          56(9)          1338-1341
Coumarins from Campylotropis hirtella (FRANCH.) SCHINDL. and Their Inhibitory Activity on Prostate Specific Antigen Secreted from LNCaP Cells
Hui-Ying HAN,Ping WEN,Hong-Wei LIU,Nai-Li WANG,and Xin-Sheng YAO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     eriophorin A
C17H14O6     ÏàËÆ¶È:70.5%
Journal of Natural Products          2005          68          1094-1098
Flavonoids from the Stem of Eriophorum scheuchzeri
Milena Maver, Emerson F. Queiroz, Jean-Luc Wolfender, and Kurt Hostettmann
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     5,7-dihydroxy-2'-methoxy-6-methylisoflavone
C17H14O5     ÏàËÆ¶È:70.5%
Journal of Natural Products          2001          64          313-317
Three New Phenolic Compounds from a Manipulated Plant Cell Culture,Mirabilis jalapa
Shu-Wei Yang, Rosa Ubillas, James McAlpine,Angela Stafford,Dawn M. Ecker, M. Kelly Talbot, and Bruce Rogers
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     2'-hydroxygenistein
    ÏàËÆ¶È:70.5%
Chemical & Pharmaceutical Bulletin          1993          41          394-396
Three New Isoflavonoid Glycosides from Lupinus luteus and L. polyphyllus¡Áarboreus
Kazutaka WATANABE,Junei KINJO and Toshihiro NOHARA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     5,7,2',6'-Tetrahydroxyflavone
C15H10O6     ÏàËÆ¶È:70.5%
Chemistry of Natural Compounds          2002          38          358-406
PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria L. GENUS. DISTRIBUTION, STRUCTURE, AND PROPERTIES
V. M. Malikov and M. P. Yuldashev
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     cajanin
C16H12O6     ÏàËÆ¶È:70.5%
Phytochemistry          2000          53          981-985
Indicanines B and C, two isoflavonoid derivatives from the root bark of Erythrina indica
Alain K. Waffo, Guy A. Azebaze, Augustin E. Nkengfack, Zacharias T. Fomum, Michele Meyer, Bernard Bodo, Fanie R. van Heerden
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     2',4',5,7-tetrahydroxyisoflavone
    ÏàËÆ¶È:70.5%
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
16 .     2',4',5,7-Tetrahydroxyisoflavone
C15H10O6     ÏàËÆ¶È:70.5%
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
17 .     2',5,6',7-Tetrahydroxy flavone
C15H10O6     ÏàËÆ¶È:70.5%
BOOK          2011          µÚÆßÕ          1633,1646
ÌìÈ»Óлú»¯ºÏÎïºË´Å¹²Õñ̼Æ×¼¯
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Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     2'-hydroxygenistein
    ÏàËÆ¶È:70.5%
Phytochemistry          1987          26          295-300
Isoflavones from Lupinus angustifolius root
Geoffrey A. Lane,Roger H. Newman
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     alpinum isoflavone
    ÏàËÆ¶È:70.5%
Chinese Traditional and Herbal Drugs          2008          39          173-175
Chemical constituents of Crotalaria ferruginea
LI Lin-zhen; YANG Xiao-sheng; ZHU Hai-yan; SHI Jing-shan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     alpinumisoflavone
    ÏàËÆ¶È:70.5%
Archives of Pharmacal Research          2005          28          1324-1327
Monoamine oxidase inhibitory constituents from the fruits of Cudrania tricuspidata
Xiang Hua Han, Seong Su Hong, Ji Sang Hwang, Seon Hwa Jeong and Ji Hye Hwang, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
21 .     Boeravinone B
C17H12O6     ÏàËÆ¶È:70.5%
Chemistry of Natural Compounds          2010          46          792-794
Cytotoxic rotenoids from Mirabilis jalapa
Jun-Ju Xu, Chen Qing, Yu-ping Lv, Ya-min Liu and Ying Liu, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
22 .     dihydroalpinumisoflavone
C20H18O5     ÏàËÆ¶È:70.5%
Journal of the Chinese Chemical Society          1996          43          515-518
Three Prenylated Isoflavones from Erythrina variegata
üS¿Ë·å(Keh-Feng Huang);î?Óô·¼(Yuh-Fang Yen)
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
23 .     compound 4
    ÏàËÆ¶È:70.5%
Journal of the Brazilian Chemical Society          1995          6          349-352
Unambiguous 1H- and 13C-NMR Assignments of Isoflavonas from Virola caducifolia.
Solange Aparecida dos Santos, Mario Geraldo de Carvalho and Raimundo Braz-Filho
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