A cell-permeable and reversible 2-benzylsulfanyl imidazole that combines the structural features of cytokine release inhibitors SKF-86002 (Cat. No.
567305) and p38 MAP kinase inhibitor SB 203580 (Cat. No.
559389). Acts as an effective inhibitor of TNF-α and IL-1β release from mononuclear cells in human whole blood and peripheral blood mononuclear cells (IC
50 = 20.3 µM and 3.65 µM for TNF-α; 2.78 µM and 0.88 µM for IL-1β, respectively). Occupies the ATP binding site of p38 MAP kinase and inhibits its activity (IC
50 = 4.0 µM).
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Product information
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Form
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Liquid
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Formulation
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A 10 mM (1 mg/236 µl) solution in DMSO.
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Primary Target
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TNF-α
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Primary Target IC50
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20.3 µM, 3.65 µM
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Secondary target
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2.78 µM and 0.88 µM for IL-1b, f p38 MAP kinase activity (IC50 = 4.0 µM)
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Molar mass
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423.5
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Protect from Light
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Yes
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Hygrocopic
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Yes
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Packaged under inert gas
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Yes
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Cell permeable
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Yes
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Purity
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>95% by HPLC
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Chemical formula
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C22H18FN3OS2
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Declaration
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Sold under license of U.S. Patent 6,432,988.
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Store and ship information
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Storage
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-20°C
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Ship
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Blue or Dry Ice
Irritant
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Safety information
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S Phrase
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S: 26
In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
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R Phrase
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R: 36/38
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