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Synthesis of lipophilic 2‐oxoamides based on γ‐aminobutyric and δ‐aminovaleric analogues and their activity against phospholipase A2
Abstract
A variety of lipophilic 2-oxoamides based on gamma-aminobutyric and delta-aminovaleric analogues were synthesized. 2-oxoamides containing a tetrazole, a thioethyl or a thioacetyl group are weak inhibitors of GIVA cPLA(2), while derivatives containing a methyl tetrazole, a diethyl phosphonate or a thioethyl group are weak inhibitors of GV sPLA(2).
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