Millipore Sigma Vibrant Logo

420119 JNK Inhibitor II - CAS 129-56-6 - Calbiochem

Übersicht

Replacement Information

Key Spec Table

CAS #Empirical Formula
129-56-6C₁₄H₈N₂O

Preis & Verfügbarkeit

Bestellnummer VerfügbarkeitVerpackung St./Pkg. Preis Menge
420119-25MG
Verfügbarkeit wird abgerufen...
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

      Kst.-Ampulle 25 mg
      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
      420119-50MG
      Verfügbarkeit wird abgerufen...
      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

          Kst.-Ampulle 50 mg
          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
          420119-5MG
          Verfügbarkeit wird abgerufen...
          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

              Kst.-Ampulle 5 mg
              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
              Description
              OverviewA potent, cell-permeable, selective, and reversible inhibitor of c-Jun N-terminal kinase (JNK) (IC50 = 40 nM for JNK-1 and JNK-2 and 90 nM for JNK-3). The inhibition is competitive with respect to ATP. Exhibits over 300-fold greater selectivity for JNK as compared to ERK1 and p38-2 MAP kinases. Inhibits the phosphorylation of c-Jun and blocks cellular expression of IL-2, IFN-γ, TNF-α, and COX-2. Blocks IL-1-induced accumulation of phospho-Jun and induction of c-Jun transcription. A 50 mM (5 mg/454 µl) solution of JNK Inhibitor II (Cat. No. 420128) in DMSO is also available.
              Catalogue Number420119
              Brand Family Calbiochem®
              SynonymsSAPK Inhibitor II, Anthra[1,9-cd]pyrazol-6(2H)-one, 1,9-pyrazoloanthrone, SP600125
              References
              ReferencesShin, M., and Boyd, Y.D. 2002. Biochim. Biophys. Acta 1589, 311.
              Bennett, B.L., et al. 2001. Proc. Natl. Acad. Sci. USA 98, 13681.
              Han, Z., et al. 2001. J. Clin. Invest. 108, 73.
              Product Information
              CAS number129-56-6
              ATP CompetitiveY
              FormYellowish orange solid
              Hill FormulaC₁₄H₈N₂O
              Chemical formulaC₁₄H₈N₂O
              ReversibleY
              Structure formula ImageStructure formula Image
              Quality LevelMQ200
              Applications
              ApplicationJNK Inhibitor II, CAS 129-56-6, is a cell-permeable, potent, selective, ATP-competitive, and reversible inhibitor of c-Jun N-terminal kinase (IC50 = 40 nM for JNK-1 & 2 & 90 nM for JNK-3).
              Biological Information
              Primary TargetJNK 1, JNK 2, JNK 3
              Primary Target IC<sub>50</sub>40 nM for JNK-1 and JNK-2 and 90 nM for JNK-3
              Purity≥98% by HPLC
              Physicochemical Information
              Cell permeableY
              Dimensions
              Materials Information
              Toxicological Information
              Safety Information according to GHS
              RTECSCB4585000
              Safety Information
              Product Usage Statements
              Storage and Shipping Information
              Ship Code Ambient Temperature Only
              Toxicity Standard Handling
              Storage -20°C
              Protect from Light Protect from light
              Do not freeze Ok to freeze
              Special InstructionsFollowing reconstitution, aliquot and freeze at -20°C. Stock solutions are stable for up to 2 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
              420119-25MG 04055977187977
              420119-50MG 04055977187991
              420119-5MG 07790788050092

              Documentation

              JNK Inhibitor II - CAS 129-56-6 - Calbiochem SDB

              Titel

              Sicherheitsdatenblatt (SDB) 

              JNK Inhibitor II - CAS 129-56-6 - Calbiochem Analysenzertifikate

              TitelChargennummer
              420119

              Literatur

              Übersicht
              Shin, M., and Boyd, Y.D. 2002. Biochim. Biophys. Acta 1589, 311.
              Bennett, B.L., et al. 2001. Proc. Natl. Acad. Sci. USA 98, 13681.
              Han, Z., et al. 2001. J. Clin. Invest. 108, 73.

              Posters

              Titel
              Human Kinome & InhibitorSelect™ Libraries

              Literaturstellen

              Titel
            • Alexandra Thiel, et al. (2006) Expression of Cyclooxygenase-2 Is Regulated by Glycogen Synthase Kinase-3beta in Gastric Cancer Cells. Journal of Biological Chemistry 281, 4564-4569.
            • Yuseok Moon, Wayne C. Glasgow and Thomas E. Eling. (2005) Curcumin suppresses interleukin 1β-mediated microsomal prostaglandin E synthase 1 (mPGES-1) by altering early growth response gene EGR-1 and other signaling pathways. Journal of Pharmacology and Experimental Therapeutics in press,.
            • Naoto Inukai, et al. (2004) A novel hydrogen peroxide-induced phosphorylation and ubiquitination pathway leading to RNA polymerase II proteolysis. Journal of Biological Chemistry 279, 8190-8195.
            • 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.

              Revision08-June-2009 RFH
              SynonymsSAPK Inhibitor II, Anthra[1,9-cd]pyrazol-6(2H)-one, 1,9-pyrazoloanthrone, SP600125
              DescriptionA potent, cell-permeable, selective, and reversible inhibitor of c-Jun N-terminal kinase (JNK) (IC50 = 40 nM for JNK-1 and JNK-2 and 90 nM for JNK-3). The inhibition is competitive with respect to ATP. Exhibits over 300-fold greater selectivity for JNK as compared to ERK1 and p38-2 MAP kinases. Inhibits the phosphorylation of c-Jun and blocks the expression of IL-2, IFN-γ, TNF-α, and COX-2 in cells. Blocks IL-1-induced accumulation of phospho-Jun and induction of c-Jun transcription.
              FormYellowish orange solid
              Intert gas (Yes/No) Packaged under inert gas
              CAS number129-56-6
              RTECSCB4585000
              Chemical formulaC₁₄H₈N₂O
              Structure formulaStructure formula
              Purity≥98% by HPLC
              SolubilityDMSO (15 mg/ml). For every 10 µM concentration of JNK Inhibitor II, include 0.1% DMSO in the culture medium. Pre-warming of culture medium and addition of BSA to the medium may enhance its solubility.
              Storage Protect from light
              -20°C
              Do Not Freeze Ok to freeze
              Special InstructionsFollowing reconstitution, aliquot and freeze at -20°C. Stock solutions are stable for up to 2 months at -20°C.
              Toxicity Standard Handling
              ReferencesShin, M., and Boyd, Y.D. 2002. Biochim. Biophys. Acta 1589, 311.
              Bennett, B.L., et al. 2001. Proc. Natl. Acad. Sci. USA 98, 13681.
              Han, Z., et al. 2001. J. Clin. Invest. 108, 73.
              Citation
            • Alexandra Thiel, et al. (2006) Expression of Cyclooxygenase-2 Is Regulated by Glycogen Synthase Kinase-3beta in Gastric Cancer Cells. Journal of Biological Chemistry 281, 4564-4569.
            • Yuseok Moon, Wayne C. Glasgow and Thomas E. Eling. (2005) Curcumin suppresses interleukin 1β-mediated microsomal prostaglandin E synthase 1 (mPGES-1) by altering early growth response gene EGR-1 and other signaling pathways. Journal of Pharmacology and Experimental Therapeutics in press,.
            • Naoto Inukai, et al. (2004) A novel hydrogen peroxide-induced phosphorylation and ubiquitination pathway leading to RNA polymerase II proteolysis. Journal of Biological Chemistry 279, 8190-8195.