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Ro 106-9920

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    Ro 106-<wbr/>9920
  • Ro 106-<wbr/>9920
Cat No: 15373
Biochemicals - Small Molecule Inhibitors
Cayman

Transcriptional activation by NF-κB is limited by IκBα binding, which masks the NF-κB nuclear localization signal that initiates nuclear translocation. Cytokines trigger a signaling cascade of kinases that target IκBα for degradation, enabling NF-κB to...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 6-(phenylsulfinyl)-tetrazolo[1,5-b]pyridazine
Correlated keywords:
  • cytokines inflammation I?B? IkappaBalpha I.kappa.B.alpha. IkBa NF-?B NF-.kappa.B NF-kappaB NF-kB transcriptions factors inflammatory diseases inhibitors inhibits inhibitions ubiquitination Ros 1069920 Ro-106-9920 Ro106-9920 Ro-1069920 Ro1069920 Ro-106 9920 Ro106 106 TNFs TNF? TNFa TNFalpha TNF.alpha. interleukins ILs ubiquitin proteasomes signals transductions intracellular signaling interleukin-1? IL-1? interleukin-1.beta. interleukin-1beta interleukin-1b IL-1.beta. IL-1beta IL-1b interleukin-6 IL-6
Product Overview:
Transcriptional activation by NF-κB is limited by IκBα binding, which masks the NF-κB nuclear localization signal that initiates nuclear translocation. Cytokines trigger a signaling cascade of kinases that target IκBα for degradation, enabling NF-κB to promote gene expression. Because NF-κB regulates the transcription of inflammatory mediators, blocking its signaling activity is regarded as an effective means to treat inflammatory diseases. Ro 106-9920 is a small molecule inhibitor of NF-κB-dependent expression of TNF-α, interleukin-1β, and interleukin-6 (IC50 50 value of 2.3 µM demonstrating little activity against the ubiquitin-activating enzyme E1 (IC50s >100 µM), the ubiquinating-conjugating enzyme E2UBCH7, nonspecific ubiquitination of cellular proteins, and 97 other molecular targets.{25615} In two different models of acute inflammation, Ro 106-9920 at 10-100 mg/kg has been shown to dose-dependently inhibit cytokine production in rat.{25615}
Size 1 mg
Shipping dry ice
CAS Number 62645-28-7
Molecular Formula C10H7N5OS
SMILES O=S(C(C=C1)=NN2C1=NN=N2)C3=CC=CC=C3
Molecular Weight 245,3
Formulation A crystalline solid
Purity ≥95%
Custom Code 2930.90
UNSPSC code 12352100

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Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

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ISO Guide 34:2009

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