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magnolol

Known as: 5,5'-diallyl-2,2'-dihydroxybiphenyl 
National Institutes of Health

Related topics

Related topics

5 relations

Broader (5)

Anti-Arrhythmia AgentsAnti-Inflammatory Agents, Non-SteroidalBiphenyl CompoundsLignans

Papers overview

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2012
2012
Anti-hepatitis B virus constituents from the stem bark of Streblus asper.
2009
2009
Multiple compounds determination and fingerprint analysis of Lidanpaishi tablet and keli by high-performance liquid chromatography.
Highly Cited
2008
Highly Cited
2008
Rapid simultaneous quantification of five active constituents in rat plasma by high-performance liquid chromatography/tandem mass spectrometry after oral administration of Da-Cheng-Qi decoction.
2007
2007
Mechanisms for the magnolol‐induced cell death of CGTH W‐2 thyroid carcinoma cells
Magnolol, a substance purified from the bark of Magnolia officialis, inhibits cell proliferation and induces apoptosis in a… 
Highly Cited
2003
Highly Cited
2003
Inhibition of smooth muscle contraction by magnolol and honokiol in porcine trachea.
Magnolol and honokiol are the two major phenolic constituents of the plant medicine "Houpo" ( Magnolia obovata), which is used in… 
2000
2000
Effects of extract and ingredients isolated from Magnolia obovata thunberg on catecholamine secretion from bovine adrenal chromaffin cells.
Highly Cited
1999
Highly Cited
1999
Antiarrhythmic Effect of Magnolol and Honokiol during Acute Phase of Coronary Occlusion in Anesthetized Rats: Influence of L-NAME and Aspirin
This study was designed to evaluate the in vivo effect of magnolol and honokiol on the acute phase of coronary ligation in the… 
1998
1998
Magnolol protects cortical neuronal cells from chemical hypoxia in rats
THE protective effect of magnolol, a component of Magnolia officinalis, against hypoxia-induced cell injury in cortical neuron… 
1995
1995
Determination of eight constituents of hsiao-cheng-chi-tang by high-performance liquid chromatography.
Highly Cited
1994
Highly Cited
1994
Biphenyl compounds are hydroxyl radical scavengers: their effective inhibition for UV-induced mutation in Salmonella typhimurium TA102.
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