(Q28279025)

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The kinetic factors that determine the affinity and selectivity for slow binding inhibition of human prostaglandin H synthase 1 and 2 by indomethacin and flurbiprofen

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The kinetic factors that determine the affinity and selectivity for slow binding inhibition of human prostaglandin H synthase 1 and 2 by indomethacin and flurbiprofen (English)

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author name string

O H Callan

1

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O Y So

2

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D C Swinney

3

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publication date

16 February 1996

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Journal of Biological Chemistry

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271

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7

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3548-54

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Inhibition of prostaglandin synthesis as a mechanism of action for aspirin-like drugs

1 reference

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Structural requirements for time-dependent inhibition of prostaglandin biosynthesis by anti-inflammatory drugs

1 reference

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Effect of inhibitor time-dependency on selectivity towards cyclooxygenase isoforms

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The X-ray crystal structure of the membrane protein prostaglandin H2 synthase-1

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Possible role for water dissociation in the slow binding of phosphorus-containing transition-state-analogue inhibitors of thermolysin

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Mechanism of selective inhibition of the inducible isoform of prostaglandin G/H synthase

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Time-dependent inhibition of platelet cyclo-oxygenase by indomethacin is slowly reversible

1 reference

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Purification, characterization and selective inhibition of human prostaglandin G/H synthase 1 and 2 expressed in the baculovirus system

1 reference

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Studies on the kinetic and chemical mechanism of inhibition of stromelysin by an N-(carboxyalkyl)dipeptide

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Solvent isotope effects on the onset of inhibition of porcine pepsin by pepstatin

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Etodolac selectively inhibits human prostaglandin G/H synthase 2 (PGHS-2) versus human PGHS-1

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10.1074/JBC.271.7.3548

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