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266788 Diacylglycerol Kinase Inhibitor II - CAS 120166-69-0 - Calbiochem

The Diacylglycerol Kinase Inhibitor II, also referenced under CAS 120166-69-0, controls the biological activity of Diacylglycerol KInase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.

FDS (Fiches de données de sécurité), certificats d’analyse (CoA) et de qualité (CoQ), dossiers, brochures et autres documents disponibles.

Synonymes: R59949, 3-{2-[4-[bis-(4-Fluorophenyl)methylene]-1-piperidinyl]ethyl}-2,3-dihydro-2-thioxo-4(1H)quinazolinone, DGK Inhibitor II

Primary Target: Diacylglycerol Kinase
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266788
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Replacement Information

Tableau de caractéristiques principal

CAS #Empirical Formula
120166-69-0C₂₈H₂₅F₂N₃OS

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266788-5MG
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      Description
      OverviewInhibits diacylglycerol kinase in isolated platelet membranes (IC50 = 300 nM) and in intact platelets (IC50 = 120 nM) by binding to the catalytic domain. A more potent analog of diacylglycerol kinase inhibitor I (Cat. No. 266785).
      Catalogue Number266788
      Brand Family Calbiochem®
      SynonymsR59949, 3-{2-[4-[bis-(4-Fluorophenyl)methylene]-1-piperidinyl]ethyl}-2,3-dihydro-2-thioxo-4(1H)quinazolinone, DGK Inhibitor II
      References
      ReferencesJiang, Y., et al. 2000. Biochem. Pharmacol. 59, 763.
      Jones, D.R., et al. 1999. J. Biol. Chem. 274, 16846.
      Rodriguez-Linares, B., et al. 1991. Biochem. Pharmacol. 41, 835.
      de Chaffoy de Courcelles, D., et al. 1989. J. Biol. Chem. 264, 3274.
      Product Information
      CAS number120166-69-0
      ATP CompetitiveN
      FormWhite solid
      Hill FormulaC₂₈H₂₅F₂N₃OS
      Chemical formulaC₂₈H₂₅F₂N₃OS
      ReversibleN
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetDiacylglycerol Kinase
      Primary Target IC<sub>50</sub>300 nM and 120 nM against diacylglycerol kinase in isolated platelet membranes and in intact platelets, respectively
      Purity≥98% by HPLC
      Physicochemical Information
      Cell permeableN
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      R PhraseR: 36/37/38

      Irritating to eyes, respiratory system and skin.
      S PhraseS: 26-36

      In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
      Wear suitable protective clothing.
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Ambient Temperature Only
      Toxicity Irritant
      Storage +15°C to +30°C
      Do not freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot, flush with an inert gas and freeze at -20°C. Stock solutions are stable for up to 6 months at -20°C.
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Référence GTIN
      266788-5MG 04055977197778

      Documentation

      Diacylglycerol Kinase Inhibitor II - CAS 120166-69-0 - Calbiochem FDS

      Titre

      Fiche de données de sécurité des matériaux (FDS) 

      Diacylglycerol Kinase Inhibitor II - CAS 120166-69-0 - Calbiochem Certificats d'analyse

      TitreNuméro de lot
      266788

      Références bibliographiques

      Aperçu de la référence bibliographique
      Jiang, Y., et al. 2000. Biochem. Pharmacol. 59, 763.
      Jones, D.R., et al. 1999. J. Biol. Chem. 274, 16846.
      Rodriguez-Linares, B., et al. 1991. Biochem. Pharmacol. 41, 835.
      de Chaffoy de Courcelles, D., et al. 1989. J. Biol. Chem. 264, 3274.

      Citations

      Titre
    • Fernando C. Gómez-Merino, et al. (2005) Arabidopsis AtDGK7, the smallest member of plant diacylglycerol kinases, displays unique biochemical features and saturates at low substrate concentration-the DGK inhibitor R59022 differentially affects AtDGK2 and AtDGK7 activity in vitro, and alters plan. Journal of Biological Chemistry 280, 34888-34899.
    • Rick B. Vega, et al. (2004) Protein Kinases C and D Mediate Agonist-Dependent Cardiac Hypertrophy through Nuclear Export of Histone Deacetylase 5. Molecular and Cellular Biology 24, 8374-8385.
      		•
      Fiche technique

      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-March-2009 RFH
      SynonymsR59949, 3-{2-[4-[bis-(4-Fluorophenyl)methylene]-1-piperidinyl]ethyl}-2,3-dihydro-2-thioxo-4(1H)quinazolinone, DGK Inhibitor II
      DescriptionInhibitor useful for elucidating roles of protein kinase C. Inhibits diacylglycerol (DAG) kinase in isolated platelet membranes (IC50 = 300 nM) and in intact platelets (IC50 = 120 nM). A more potent analog of DAG kinase inhibitor I.
      FormWhite solid
      CAS number120166-69-0
      Chemical formulaC₂₈H₂₅F₂N₃OS
      Structure formulaStructure formula
      Purity≥98% by HPLC
      SolubilityDMSO (12.5 mg/ml)
      Storage +15°C to +30°C
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot, flush with an inert gas and freeze at -20°C. Stock solutions are stable for up to 6 months at -20°C.
      Toxicity Irritant
      ReferencesJiang, Y., et al. 2000. Biochem. Pharmacol. 59, 763.
      Jones, D.R., et al. 1999. J. Biol. Chem. 274, 16846.
      Rodriguez-Linares, B., et al. 1991. Biochem. Pharmacol. 41, 835.
      de Chaffoy de Courcelles, D., et al. 1989. J. Biol. Chem. 264, 3274.
      Citation
    • Fernando C. Gómez-Merino, et al. (2005) Arabidopsis AtDGK7, the smallest member of plant diacylglycerol kinases, displays unique biochemical features and saturates at low substrate concentration-the DGK inhibitor R59022 differentially affects AtDGK2 and AtDGK7 activity in vitro, and alters plan. Journal of Biological Chemistry 280, 34888-34899.
    • Rick B. Vega, et al. (2004) Protein Kinases C and D Mediate Agonist-Dependent Cardiac Hypertrophy through Nuclear Export of Histone Deacetylase 5. Molecular and Cellular Biology 24, 8374-8385.
      		•