Structure-activity relationships of acetylated flavone glycosides from Galeopsis ladanum L. (Lamiaceae)

Food Chemistry

Volumn 120, Issue 3, 2010, Pages 679-683

  Uriarte Pueyo, Inigo ^a   Calvo, María Isabel ^a  

^a UNIVERSITY OF NAVARRA   (Spain)

Author keywords

Acetylated flavones; Acetylcholinesterase inhibitors; Antioxidant activity; Galeopsis ladanum; Hypolaetin; Isoscutellarein; Neuroprotective effect

Indexed keywords

ACETYLCHOLINESTERASE; ANTIOXIDANT; CHOLINESTERASE INHIBITOR; FLAVONE DERIVATIVE; FLAVONOID; GLYCOSIDE; HYDROXYL GROUP; HYPOLAETIN 4' METHYL ETHER 7 (2'' ALLOSYL)GLUCOSIDE DIACETYLATED; HYPOLAETIN 4' METHYL ETHER 7 (2'' ALLOSYL)GLUCOSIDE MONOACETYLATED; HYPOLAETIN 7 (2'' ALLOSYL)GLUCOSIDE MONOACETYLATED; ISOSCUTELLAREIN 4' METHYL ETHER 7 (2'' ALLOSYL)GLUCOSIDE MONOACETYLATED; ISOSCUTELLAREIN 7 (2'' ALLOSYL)GLUCOSIDE DIACETYLATED; ISOSCUTELLAREIN 7 (2'' ALLOSYL)GLUCOSIDE MONOACETYLATED; UNCLASSIFIED DRUG;

ALZHEIMER DISEASE; ANGIOSPERM; ANTIOXIDANT ACTIVITY; ARTICLE; CELL SURVIVAL; CYTOTOXICITY; DRUG ACETYLATION; DRUG ACTIVITY; DRUG HYDROXYLATION; DRUG ISOLATION; DRUG STRUCTURE; GALEOPSIS LADANUM; HUMAN; HUMAN CELL; MASS SPECTROMETRY; METHYLATION; NEUROPROTECTION; NONHUMAN; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ACTIVITY RELATION; ULTRAVIOLET SPECTROPHOTOMETRY; ULTRAVIOLET SPECTROSCOPY;

GALEOPSIS LADANUM; LAMIACEAE;

EID: 74049158915     PISSN: 03088146     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.foodchem.2009.10.060     Document Type: Article

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