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Cellular Processes » Signal Transduction » Cytokine and NF-κB Signaling » NF-κB & IκB » Ro 106-9920
Ro 106-9920Cat No. 1778 |
Price and Availability |
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Chemical Name: 6-(Phenylsulfinyl)tetrazolo[1,5-b]pyridazine |
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Biological Activity
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
M.Wt:245.26
Formula:C10H7N5OS
Solubility:Soluble to 5 mM in ethanol and to 100 mM in DMSO
Purity: >99 %
Storage:Store at +4°C
CAS No:[62645-28-7]
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis and MSDS.
Resources
Certificate of Analysis / MSDS
Certificate of Analysis: View current batch
Material Safety Data Sheet: View current batch
References
Conalty et al (1976) Anticancer agents. XII. Pyridazine and benzodiazine derivatives. Proc.R.Ir.Acad. 76 151. Swinney et al (2002) A small molecule ubiquitination inhibitor blocks NF-kB-dependent cytokine expression in cells and rats. J.Biol.Chem. 277 23573. Baginski et al (2002) Glucocorticoid modulation of MUC5AC secretion in H292 cells. Am.Soc.Cell Biol.Abstr. 765.If you know of a useful citation for this product please let us know.
Keywords: Ro 106-9920, inhibitors, NF-κB, NF-kappaB, NF-kB, activation, Transcription, Factors, Nuclear, Factor, Kappa, B, Ro106-9920
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