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Sci. Pharm.
Volume 77
Issue 7
10.3797/scipharm.oephg.21.PO-25
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Scientia Pharmaceutica is published by MDPI from Volume 84 Issue 3 (2016). Previous articles were published by another publisher in Open Access under a CC-BY (or CC-BY-NC-ND) licence, and they are hosted by MDPI on mdpi.com as a courtesy and upon agreement with Austrian Pharmaceutical Society (Österreichische Pharmazeutische Gesellschaft, ÖPhG).
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Abstract

Synthesis of Deuterated Analogs of Honokiol

by
A. HÜFNER
1,* and
W. SCHÜHLY
2
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 / Accepted: 16 April 2009 / Published: 16 April 2009
Versions Notes

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 Style

HÜFNER, 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

APA Style

HÜFNER, A., & SCHÜHLY, W. (2009). Synthesis of Deuterated Analogs of Honokiol. Scientia Pharmaceutica, 77(Posters (PO)), 224. https://doi.org/10.3797/scipharm.oephg.21.PO-25

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