(E)-phenyl- and -heteroaryl-substituted O-benzoyl- (or acyl)oximes as lipoprotein-associated phospholipase A2 inhibitors
A series of (E)-phenyl- and -heteroaryl-substituted O-benzoyl- (or acyl)oximes 3a-n were synthesized for evaluating their human lipoprotein-associated phospholiphase A2 (Lp-PLA2) inhibitory activities. The less lipophilic derivatives 3a-c showed the most potent in vitro inhibitory activity on human...
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Veröffentlicht in: | Bioorganic & medicinal chemistry letters 2005-03, Vol.15 (5), p.1525-1527 |
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Sprache: | eng |
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