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[Synthesis of lipoxygenase inhibitors. 1. Synthesis of open-ring amidrazones]
1Institut für Pharmazeutische Chemie, Fachbereich Pharmazie, Martin-Luther-Universität Halle-Wittenberg.
Die Pharmazie
|May 1, 1993
Abstract:
The synthesis of some amidrazones as bioisosteric diazaallyl radicals is described starting from the reaction mechanism of the lipoxygenases which postulates the existence of a radical after hydrogen abstraction from the arachidonic acid, N1,N3-diaryl-, N1-aryl-N3-alkyl-benzamidrazones and N1-arylacetamidrazones are strong inhibitors of the soja lipoxygenase.