The synthesis of the structure, 1, assigned to the anti-inflammatory natural product myrsinoic acid F is reported together with a means for preparing its Z-isomer 21. While neither of these compounds corresponds to the natural product, both of them are anti-inflammatory agents (as determined using a mouse ear edema assay) with congener 1 being notably more potent than the widely prescribed NSAID indometacin.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.orglett.8b01558 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!