Biochem/physiol Actions
Primary TargetMIF dopachrome tautomerase
Cell permeable: yes
General description
A cell-permeable isoxazoline compound that displays anti-inflammatory properties. Inhibits MIF dopachrome tautomerase activity by binding to its catalytic active site (IC50 = 7 µM for D-dopachrome tautomerase) and suppresses the production of TNFα, PGE2 and COX-2 in human monocytes and arachidonic acid in RAW 264.7 macrophages. Shown to exhibit antidiabetogenic properties in immunoinflammatory diabetic mouse model.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Other Notes
Cvetkovic, I., et al. 2005. Endocrinology146, 2942.Lubetsky, J.B., et al. 2002. J. Biol. Chem.277, 24976.
Packaging
Packaged under inert gas
10 mg in Glass bottle
Physical form
A 50 mM (10 mg/850 µL) sterile-filtered solution of MIF Antagonist, ISO-1 (Cat. No. 475837) in DMSO.
Reconstitution
Following initial thaw, aliquot and freeze (-70°C). Aliquots are stable for up to 1 year at -70°C.
Warning
Toxicity: Irritant (B)
This product has met the following criteria to qualify for the following awards: