Synthesis of Deuterated Analogs of Honokiol
1
Institute of Pharm. Sciences, Dept. of Pharm. Chemistry, University of Graz, Universitätsplatz 1, 8010 Graz, Austria
2
Institute of Pharm. Sciences, Dept. of Pharmacognosy, University of Graz, Universitätsplatz 4, 8010 Graz, Austria
*
Author to whom correspondence should be addressed.
Sci. Pharm. 2009, 77(7), 224; https://doi.org/10.3797/scipharm.oephg.21.PO-25
Submission received: 16 April 2009
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Accepted: 16 April 2009
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Published: 16 April 2009
Abstract
The genus Magnolia plays a role in American as well as in Asian medicinal systems such as TCM or Japanese Kampo medicine [1, 2]. Main lignan constituents in the seeds of the north american Magnolia grandiflora are honokiol (1) and 4'-O-methyl-honokiol. They are known to possess anti-inflammatory activities with COX-2 inhibitory activity (IC50) of about 0.1 to 3 μM.
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MDPI and ACS Style
HÜFNER, A.; SCHÜHLY, W. Synthesis of Deuterated Analogs of Honokiol. Sci. Pharm. 2009, 77, 224. https://doi.org/10.3797/scipharm.oephg.21.PO-25
AMA Style
HÜFNER A, SCHÜHLY W. Synthesis of Deuterated Analogs of Honokiol. Scientia Pharmaceutica. 2009; 77(Posters (PO)):224. https://doi.org/10.3797/scipharm.oephg.21.PO-25
Chicago/Turabian StyleHÜFNER, A., and W. SCHÜHLY. 2009. "Synthesis of Deuterated Analogs of Honokiol" Scientia Pharmaceutica 77, Posters (PO): 224. https://doi.org/10.3797/scipharm.oephg.21.PO-25
