DETECTION OF A NEW SERIES OF MONOAMINE OXIDASE INHIBITORS

  • 甲斐 麻美子
    Faculty of Pharmaceutical Sciences, Kyushu University
  • 野田 敦子
    Faculty of Pharmaceutical Sciences, Kyushu University
  • 野田 浩司
    Department of Hospital Pharmacy, School of Medicine, University of Occupational and Environmental Health, Japan
  • 後藤 茂
    Faculty of Pharmaceutical Sciences, Kyushu University

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抄録

A new series of monoamine oxidase (MAO) inhibitors structurally analogous to tetrazolo [5,1-a] phthalazine (Tetra-P) was detected using rat brain mitochondrial MAO. In the tricyclic group, naphtetrazole (NTE) indicated a marked potency of MAO inhibition almost equal to that of iproniazid, and naphtriazole (NTR) showed similar potency as did Tetra-P. The nonselective and competitive inhibition for both types, MAO-A and MAO-B, was observed in some Tetra-P analogues.

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