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ding123456: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, 5·Ö 2015-03-15 08:34:38
1 .     cardamomin
    ÏàËÆ¶È:100%
Phytochemistry          1981          20          2503-2506
Phenolic compounds from the rhizomes of Alpinia speciosa
Hideji Itokawa, Makoto Morita, Susumu Mihashi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     Cardamonin
C16H14O4     ÏàËÆ¶È:87.5%
Natural Product Sciences          2007          13          110-113
Cytotoxic Constituents from Boesenbergia pandurate (Roxb.) Schltr
Ching, Amy Yap Li; Lian, Gwendoline Ee Cheng; Rahmani, Mawardi; Khalid, Kaida; Sukari, Mohd Aspollah
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     2',4'-dihydroxy-6'-methoxy-3'-methylchalcone
C17H16O4     ÏàËÆ¶È:82.3%
Zeitschrift f¨¹r Naturforschung C          2004          59          86-92
Prolyl Endopeptidase Inhibitors from Syzygium samarangense (Blume) Merr. & L. M. Perry
E. C.Amor, I. M. Villaseñor, A. Yasin, and M. I. Choudhary
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     stercurensin
C17H16O4     ÏàËÆ¶È:82.3%
Phytotherapy Research          2005          19          246-251
Antihyperglycaemic flavonoids from Syzygium samarangense (Blume) Merr. and Perry
Ma. Hanshella C. Resurreccion-Magno, Irene M. Villaseñor, Nobuyuki Harada and Kenji Monde
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     2',4'-dihydroxy-6'-methoxy-3'-methylchalcone
C17H16O4     ÏàËÆ¶È:82.3%
Pharmaceutical Biology          2007          45          777-783
Cytotoxic C-Methylated Chalcones from Syzygium samarangense.
Evangeline C. Amor, Irene M. Villaseñor, Rowena Antemano, Zeebah Perveen, Gisela P. Concepcion, M.I. Choudhary
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     2',4'-dihydroxy-6'-methoxychalcone
C16H14O4     ÏàËÆ¶È:77.7%
Fitoterapia          2012          83          932-940
Phytochemical and antimicrobial investigations of stilbenoids and flavonoids isolated from three species of Combretaceae
David R. Katerere, Alexander I. Gray, Robert J. Nash, Roger D. Waigh
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     stercurensin
    ÏàËÆ¶È:75%
Planta Medica          2004          70          1237-1239
Isolation and Immunomodulatory Effect of Flavonoids from Syzygium samarangense
Yuh-Chi Kuo , Li-Ming Yang , Lie-Chwen Lin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     cardamonin
C16H14O4     ÏàËÆ¶È:75%
Phytochemistry          1998          47          1117-1123
Stilbenes, monoterpenes, diarylheptanoids, labdanes and chalcones from Alpinia katsumadai
Koon-Sin Ngo, Geoffrey D. Brown
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     compound 4
    ÏàËÆ¶È:75%
Phytochemistry          1988          27          3937-3939
A chalcone derivative from the bark of Lindera umbellata
Hiroko Shimomura,Yutaka Sashida,Yoshihiro Mimaki,Motomu Oohara,Yasuomi Fukai
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     Uvangoletin
C16H16O4     ÏàËÆ¶È:75%
Phytochemistry          1980          19          2036-2038
Dihydrochalcones from Uvaria angolensis
Charles D. Hufford, Babajide O. Oguntimein
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     (E)-1-(2,4-Dihydroxy-6-methoxyphenyl)-3-phenylprop-2-en-1-one
    ÏàËÆ¶È:75%
Archives of Pharmacal Research          2007          30          1359-1367
Structural requirements of 2',4',6'-tris(methoxymethoxy) chalcone derivatives for anti-inflammatory activity: The importance of a 2'-hydroxy moiety
Feng Jin, Xing Yu Jin, Ying Lan Jin, Dae Won Sohn and Soon-Ai Kim, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     2',4'-dihydroxy-3',6'-dimethoxychalcone
    ÏàËÆ¶È:70.5%
Natural Product Sciences          2004          10          207-210
Constituents of Lindera Erythrocarpa Stem Bark
Lee, Hak-Ju; Park, Young-Ki; Park, Il-Kwon; Shin, Sang-Chul
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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