Synthesis of Deuterated Analogs of Honokiol
AbstractThe 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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HÜFNER, A.; SCHÜHLY, W. Synthesis of Deuterated Analogs of Honokiol. Sci. Pharm. 2009, 77, 224.
HÜFNER A, SCHÜHLY W. Synthesis of Deuterated Analogs of Honokiol. Scientia Pharmaceutica. 2009; 77(Posters (PO)):224.Chicago/Turabian Style
HÜFNER, A.; SCHÜHLY, W. 2009. "Synthesis of Deuterated Analogs of Honokiol." Sci. Pharm. 77, Posters (PO): 224.