Ro 106-9920
Chemical Name: 6-(Phenylsulfinyl)tetrazolo[1,5-b]pyridazine
Purity: ≥99%
Biological Activity
Ro 106-9920 is an inhibitor of NF-κB activation, possibly via selective inhibition of LPS- and TNF-α-induced IκBα ubiquitination (IC50 = 3 μM). Blocks subsequent production of TNF-α, IL-1β and IL-6. Inhibits mucin production in an in vitro model of COPD, and is anti-inflammatory following oral administration in vivo. Also weakly inhibits EGFR, 5-lipoxygenase and iNOS.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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Anticancer agents. XII. Pyridazine and benzodiazine derivatives.
Conalty et al.
Proc.R.Ir.Acad.B., 1976;76:151 -
A small molecule ubiquitination inhibitor blocks NF-κB-dependent cytokine expression in cells and rats.
Swinney et al.
J.Biol.Chem., 2002;277:23573 -
Glucocorticoid modulation of MUC5AC secretion in H292 cells.
Baginski et al.
Am.Soc.Cell Biol.Abstr., 2002;:765
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Citations for Ro 106-9920
The citations listed below are publications that use Tocris products. Selected citations for Ro 106-9920 include:
4 Citations: Showing 1 - 4
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Galectin-3 is required for the microglia-mediated brain inflammation in a model of Huntington's disease.
Authors: Siew Et al.
Nat Commun 2019;10:3473
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ATF4 is a novel regulator of MCP-1 in microvascular endothelial cells.
Authors: Huang Et al.
J Inflamm (Lond) 2015;12:31
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Ligand engagement of Toll-like receptors regulates their expression in cortical microglia and astrocytes.
Authors: Marinelli Et al.
PLoS One 2015;12:244
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Regulation of neutrophil extracellular trap formation by anti-inflammatory drugs.
Authors: Lapponi Et al.
J Pharmacol Exp Ther 2013;345:430
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