Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5166349 | Phytochemistry | 2009 | 6 Pages |
Abstract
Di-nor-benzofuran neolignan aldehydes, (ocophyllal A-B) 1-2, and macrophyllin-type bicyclo[3.2.1]octanoid neolignans (ocophyllol A-C) 3-5, as well as 2â²-epi-guianin 6 and (+)-licarin B 7, were isolated from leaves of Ocotea macrophylla. Their structures and absolute configurations were determined by spectroscopic analyses. Inhibition of platelet activating factor (PAF)-induced aggregation of rabbit platelets were tested with neolignans 1-7. Although compound 6 was the most potent PAF-antagonist, compounds 3-5 showed some activity.
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Authors
Ericsson D. Coy-Barrera, Luis E. Cuca-Suárez, Michael Sefkow,