Synthesis, cytotoxicity, and antioxidative activity of minor prenylated chalcones from Humulus lupulus

Journal of Natural Products

Volumn 71, Issue 7, 2008, Pages 1237-1241

  Vogel, Susanne ^a   Heilmann, Jörg ^a  

^a UNIVERSITY OF REGENSBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

1'',2'' DIHYDROXANTHOHUMOL C (2'',2'' DIMETHYL 3'',4'' DIHYDRO (2H) PYRANO[2'',3'':3',4'] 2',4 DIHYDROXY 6' METHOXYCHALCONE; 2',4 DIHYDROXY 4',6' DIMETHOXY 3' METHYLCHALCONE; 2',4 DIHYDROXY 4',6' DIMETHOXYCHALCONE (FLAVOWAKIN); 2',4,4' TRIHYDROXY 6' METHOXY 3',5' DIPRENYLCHALCONE (5' PRENYLXANTHOHUMOL); 2',4,4',6' TETRAHYDROXY 3' GERANYLCHALCONE (3' GERANYLCHALCONARINGENIN); 3' GERANYL 2',4,4' TRIHYDROXY 6' METHOXYCHALCONE (3' GERANYL 6' O METHYLCHALCONARINGENIN); 4,4',6' TRIHYDROXY 2' METHOXY 3' PRENYLCHALCONE (2' O METHYL 3' PRENYLCHALCONARINGENIN, XANTHOFLORIANOL); CHALCONE DERIVATIVE; OXYGEN RADICAL; TROLOX C; XANTHOHUMOL C; XANTHOHUMOL H;

ANTIOXIDANT ACTIVITY; ARTICLE; CYTOTOXICITY; DRUG STRUCTURE; DRUG SYNTHESIS; FLUORESCENCE; HELA CELL; HUMULUS LUPULUS; IC 50;

ANTIOXIDANTS; CHALCONES; HELA CELLS; HUMANS; HUMULUS; INHIBITORY CONCENTRATION 50; MOLECULAR STRUCTURE; PROPIOPHENONES;

HUMULUS LUPULUS;

EID: 49049089964     PISSN: 01633864     EISSN: None     Source Type: Journal    
DOI: 10.1021/np800188b     Document Type: Article

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