XT2

2 Cited Publications
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Based on 2 publication(s) in Google Scholar

XT2 is a potent, orally active, and selective inhibitor of NF-κB-inducing kinase (NIK) with an IC50 of 9.1 nM. XT2 suppresses CCl4-induced upregulation of ALT, a key biomarker of acute liver injury. XT2 also decreases immune cell infiltration into the injured liver tissue. XT2 has the potential for the research of liver inflammatory diseases. XT2 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

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  • Reinheit: 99.60%
  • CAS. Nr.: 2582816-37-1
  • Formel: C19H14FN5OS
  • Molecular Weight:379.41
  • Speicherung:
    Powder   -20°C, 3 years , 4°C, 2 years ; In solvent   -80°C, 6 months , -20°C, 1 month
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Publications Citing Use of MedChemExpress (MCE) XT2

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