Traxanox is an orally available diuretic that enhances phagocytosis of yeast granules by mouse peritoneal macrophages and rat peritoneal polymorphonuclear leukocytes in vitro. Traxanox inhibits IgE-mediated histamine release and cyclic AMP phosphodiesterase activity.Traxanox exhibits anti-inflammatory activity, as it inhibits the anaphylactoid reaction and reduces pleural fluid accumulation in experimental models of inflammation. Traxanox also demonstrates a synergistic effect when combined with hydrocortisone or indomethacin in suppressing adjuvant arthritis in rats.
Molekulargewicht:
299.67
CAS Nummer:
[58712-69-9]
Formel:
C13H6ClN5O2
Target-Kategorie:
Histamine Receptor,Phosphodiesterase (PDE)
Anwendungsbeschreibung:
MCE Product type: Reference compound
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