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Luteolin

Known as: 3',4',5,7-Tetrahydroxyflavone, Luteolin [Chemical/Ingredient], Luteoline 
5,7,3',4'-tetrahydroxy-flavone, one of the FLAVONES.
National Institutes of Health

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22 relations

Narrower (13)

6-hydroxyluteolinIsoorientin-6-O-glucosidehomoorientinluteolin 5-rutinoside
In BloodProcess of secretionagonistsantagonists & inhibitors

Papers overview

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Highly Cited
2010
Highly Cited
2010
Luteolin inhibits microglia and alters hippocampal-dependent spatial working memory in aged mice.
A dysregulated overexpression of inflammatory mediators by microglia may facilitate cognitive aging and neurodegeneration… 
Highly Cited
2007
Highly Cited
2007
Luteolin protects rat PC12 and C6 cells against MPP+ induced toxicity via an ERK dependent Keap1-Nrf2-ARE pathway.
Oxidative stress is central to neuronal damage in neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease… 
Highly Cited
2003
Highly Cited
2003
Inhibition of 15-lipoxygenases by flavonoids: structure-activity relations and mode of action.
Highly Cited
2002
Highly Cited
2002
Inhibition of LPS‐stimulated pathways in macrophages by the flavonoid luteolin
We have previously shown that the flavonoid luteolin inhibits the expression of pro‐inflammatory molecules induced by LPS. In the… 
Highly Cited
2002
Highly Cited
2002
Wogonin and fisetin induce apoptosis in human promyeloleukemic cells, accompanied by a decrease of reactive oxygen species, and activation of caspase 3 and Ca(2+)-dependent endonuclease.
Highly Cited
2000
Highly Cited
2000
Flavonols from Heterotheca inuloides: tyrosinase inhibitory activity and structural criteria.
Highly Cited
2000
Highly Cited
2000
On the ability of four flavonoids, baicilein, luteolin, naringenin, and quercetin, to suppress the fenton reaction of the iron-ATP complex
Four flavonoids, baicilein, luteolin, naringenin, and quercetin were investigated for their ability to suppress the Fenton… 
Highly Cited
1994
Highly Cited
1994
Terpenoids from Salvia sclarea.
Highly Cited
1990
Highly Cited
1990
Structure-activity relationships of polymethoxyflavones and other flavonoids as inhibitors of non-enzymic lipid peroxidation.
Highly Cited
1989
Highly Cited
1989
Protein kinase C inhibition by plant flavonoids. Kinetic mechanisms and structure-activity relationships.
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