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Bioorg Med Chem Lett ; 18(1): 409-13, 2008 Jan 01.
Article in English | MEDLINE | ID: mdl-17981034

ABSTRACT

Matrix metalloproteinase-9 (MMP-9) has been implicated in the breakdown of the blood-brain barrier during cerebral ischemia. As a result, inhibition of MMP-9 may have utility as a therapeutic intervention in stroke. Towards this end, we have synthesized a series of 1-hydroxy-2-pyridinones that have excellent in vitro potency in inhibiting MMP-9 in addition to MMP-2. Representative compounds also demonstrate good efficacy in the mouse transient mid-cerebral artery occlusion (tMCAO) model of cerebral ischemia.


Subject(s)
Brain Ischemia/drug therapy , Matrix Metalloproteinase Inhibitors , Protease Inhibitors/chemical synthesis , Pyridones/chemical synthesis , Pyridones/pharmacology , Administration, Oral , Animals , Biological Availability , Disease Models, Animal , Inhibitory Concentration 50 , Male , Mice , Mice, Inbred C57BL , Models, Molecular , Protease Inhibitors/chemistry , Protease Inhibitors/pharmacokinetics , Protease Inhibitors/pharmacology , Pyridones/chemistry , Pyridones/pharmacokinetics , Structure-Activity Relationship , Sulfonamides/chemical synthesis , Sulfonamides/chemistry , Sulfonamides/pharmacokinetics , Sulfonamides/pharmacology , Zinc/chemistry , Zinc/metabolism
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