Artigo Revisado por pares

Synthesis of 5-Substituted Pyrrolo[1,2-b]pyridazines with Antioxidant Properties

2001; Wiley; Volume: 334; Issue: 1 Linguagem: Inglês

10.1002/1521-4184(200101)334

ISSN

1521-4184

Autores

Ole Benny Østby, Lise‐Lotte Gundersen, Frode Rise, Øyvind Antonsen, Kjetil Fosnes, Vibeke Larsen, Aalt Bast, Ilse Custers, Guido R.M.M. Haenen,

Tópico(s)

Retinoids in leukemia and cellular processes

Resumo

5-Substituted pyrrolo[1,2-b]pyridazines have been prepared by cyclisation of pyridazine with diphenylcyclopropenone followed by further functionalisations in the pyrrolo[1,2-b]pyridazine 5-position. Several compound exhibit profound inhibition of lipid peroxidation in vitro. Lipid peroxidation of boiled rat liver microsomes was induced by ascorbic acid/FeSO4 and the peroxidation was determined by measuring the thiobarbituric acid reactive material.

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