Millipore Sigma Vibrant Logo

401489 IKK Inhibitor X - CAS 431898-65-6 - Calbiochem

401489
  
Preis wird abgerufen...
Preis nicht abrufbar
Die Mindestmenge muss ein Vielfaches sein von
Maximum Quantity is
Bei Bestätigung Weitere Informationen
Sie haben () gespart
 
Bitte erfragen
Eingeschränkte Verfügbarkeit
Eingeschränkte Verfügbarkeit
Lieferbar 
Produkt wurde eingestellt
Begrenzter Lagerbestand
Bestätigung der Verfügbarkeit erforderlich
    Restmenge: Angebot folgt
      Restmenge: Angebot folgt
      Bitte erfragen
      Kontakt zum Kundenservice
      Contact Customer Service

       

      Kontakt zum Kundenservice

      Übersicht

      Replacement Information

      Key Spec Table

      CAS #Empirical Formula
      431898-65-6C₁₇H₁₁ClN₄O
      Description
      Overview

      This product has been discontinued.



      A cell-permeable β-carboline compound that displays anti-inflammatory properties. Acts as a potent, ATP-competitive, and reversible inhibitor of IKK (IC50 = 88 nM) with selectivity over 14 other commonly studied kinases (IC50 > 100 µM), including NF-κB inducing kinase. Blocks cellular IκBα phosphorylation and NF-κB activation (EC50 = 5 µM in TNF-α-treated HeLa cells) in vitro and reduces TNF-α release in plasma of LPS-challenged mice in vivo (50 mg/ml, p.o.).

      Catalogue Number401489
      Brand Family Calbiochem®
      SynonymsN-(6-Chloro-9H-β-carbolin-8-yl)nicotinamide, PS-1145
      References
      ReferencesCatley, M.C., et al. 2006. Mol. Pharmacol. 70, 697.
      Wen, D., et al. 2006. J. Pharm. Exp. Ther. 317, 989.
      Castro, A.C., et al. 2003. Bioorg. Med. Chem. Lett. 13, 2419.
      Hideshima, T., et al. 2002. J. Biol. Chem. 277, 16639.
      Product Information
      CAS number431898-65-6
      ATP CompetitiveY
      FormYellow solid
      Hill FormulaC₁₇H₁₁ClN₄O
      Chemical formulaC₁₇H₁₁ClN₄O
      ReversibleY
      Structure formula ImageStructure formula Image
      Applications
      Biological Information
      Primary TargetIKK
      Primary Target IC<sub>50</sub>88 nM against IKK
      Purity≥98% by HPLC
      Physicochemical Information
      Cell permeableY
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Ambient Temperature Only
      Toxicity Standard Handling
      Storage +2°C to +8°C
      Protect from Light Protect from light
      Do not freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.
      Packaging Information
      Packaged under inert gas Packaged under inert gas
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Bestellnummer GTIN
      401489 0

      Documentation

      IKK Inhibitor X - CAS 431898-65-6 - Calbiochem Analysenzertifikate

      TitelChargennummer
      401489

      Literatur

      Übersicht
      Catley, M.C., et al. 2006. Mol. Pharmacol. 70, 697.
      Wen, D., et al. 2006. J. Pharm. Exp. Ther. 317, 989.
      Castro, A.C., et al. 2003. Bioorg. Med. Chem. Lett. 13, 2419.
      Hideshima, T., et al. 2002. J. Biol. Chem. 277, 16639.
      Datenblatt

      Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

      Revision13-April-2011 RFH
      SynonymsN-(6-Chloro-9H-β-carbolin-8-yl)nicotinamide, PS-1145
      DescriptionA cell-permeable β-carboline compound that displays anti-inflammatory properties. Acts as a potent, ATP-competitive, and reversible inhibitor of IKK (IC50 =88 nM) with selectivity over 14 other commonly studied kinases (IC50 > 100 µM), including NF-κB inducing kinase. Blocks cellular IκBα phosphorylation and NF-κB activation (EC50 = 5 µM in TNF-α-treated HeLa cells) in vitro and reduces TNF-α release in plasma of LPS-challenged mice in vivo (50 mg/ml p.o.).
      FormYellow solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number431898-65-6
      Chemical formulaC₁₇H₁₁ClN₄O
      Structure formulaStructure formula
      Purity≥98% by HPLC
      SolubilityDMSO (50 mg/ml)
      Storage Protect from light
      +2°C to +8°C
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.
      Toxicity Standard Handling
      ReferencesCatley, M.C., et al. 2006. Mol. Pharmacol. 70, 697.
      Wen, D., et al. 2006. J. Pharm. Exp. Ther. 317, 989.
      Castro, A.C., et al. 2003. Bioorg. Med. Chem. Lett. 13, 2419.
      Hideshima, T., et al. 2002. J. Biol. Chem. 277, 16639.