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551476 InSolution™ Q-VD-OPh, Non-O-methylated - Calbiochem

Übersicht

Replacement Information

Key Spec Table

Empirical Formula
C₂₆H₂₅F₂N₃O₆

Preis & Verfügbarkeit

Bestellnummer VerfügbarkeitVerpackung St./Pkg. Preis Menge
551476-1MG
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      Kst.-Ampulle 1 mg
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      Die Mindestmenge muss ein Vielfaches sein von
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      551476-5MG
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      Lieferbar 
      Produkt wurde eingestellt
      Begrenzter Lagerbestand
      Bestätigung der Verfügbarkeit erforderlich
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          Kontakt zum Kundenservice
          Contact Customer Service

          Glasflasche 5 mg
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          Description
          OverviewA cell-permeable, irreversible, broad-spectrum caspase inhibitor (IC50 = 50, 100, 430, and <25 nM for caspase-1,-8, -9, and -3, respectively) with effective antiapoptotic properties against all major caspase-mediated cellular apoptosis pathways. Exhibits no cytotoxic effects even at extremely high concentrations. Shown to reduce ischemic brain damage and stroke-induced programmed cell death in thymus and spleen.
          Catalogue Number551476
          Brand Family Calbiochem®
          SynonymsN-(2-Quinolyl)valyl-aspartyl-(2,6-difluorophenoxy)methyl Ketone
          References
          ReferencesBraun, J.S., et al. 2007. Exp. Neurol. 206, 183.
          Caserta, T.M., et al. 2003. Apoptosis 8, 345.
          Rebbaa, A., et al. 2003. Oncogene 22, 2805.
          Product Information
          ATP CompetitiveN
          FormLiquid
          FormulationSupplied as a 10 mM (1 mg/195 µl) solution in DMSO.
          Hill FormulaC₂₆H₂₅F₂N₃O₆
          Chemical formulaC₂₆H₂₅F₂N₃O₆
          Hygroscopic Hygroscopic
          ReversibleN
          Structure formula ImageStructure formula Image
          Quality LevelMQ100
          Applications
          Biological Information
          Primary Targetcaspase-1
          Primary Target IC<sub>50</sub>50, 100, 430, and <25 nM for caspase-1,-8, -9, and -3, respectively
          Purity≥90% by HPLC
          Physicochemical Information
          Cell permeableY
          Peptide SequenceQ-Val-Asp-CH₂-OPh
          Dimensions
          Materials Information
          Toxicological Information
          Safety Information according to GHS
          Safety Information
          Product Usage Statements
          Storage and Shipping Information
          Ship Code Shipped with Blue Ice or with Dry Ice
          Toxicity Irritant
          Storage -20°C
          Protect from Light Protect from light
          Hygroscopic Hygroscopic
          Do not freeze Ok to freeze
          Special InstructionsFollowing initial thaw, aliquot and freeze (-20°C).
          Packaging Information
          Packaged under inert gas Packaged under inert gas
          Transport Information
          Supplemental Information
          Specifications
          Global Trade Item Number
          Bestellnummer GTIN
          551476-1MG 04055977268898
          551476-5MG 04055977268904

          Documentation

          InSolution™ Q-VD-OPh, Non-O-methylated - Calbiochem SDB

          Titel

          Sicherheitsdatenblatt (SDB) 

          InSolution™ Q-VD-OPh, Non-O-methylated - Calbiochem Analysenzertifikate

          TitelChargennummer
          551476

          Literatur

          Übersicht
          Braun, J.S., et al. 2007. Exp. Neurol. 206, 183.
          Caserta, T.M., et al. 2003. Apoptosis 8, 345.
          Rebbaa, A., et al. 2003. Oncogene 22, 2805.

          Broschüre

          Titel
          Caspases and other Apoptosis Related Tools Brochure

          Literaturstellen

          Titel
        • Braun, J.S., et al. 2007. Exp. Neurol. 206, 183.
        • Jessica H. Dworet and Judy L. Meinkoth. 2006.Molecular Endocrinology 20, 1112.
        • Ademi E. Santiago-Walker, et al. (2005) Protein Kinase C δ Stimulates Apoptosis by Initiating G1 Phase Cell Cycle Progression and S Phase Arrest. Journal of Biological Chemistry 280, 32107-32114.
        • 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.

          Revision28-February-2012 RFH
          SynonymsN-(2-Quinolyl)valyl-aspartyl-(2,6-difluorophenoxy)methyl Ketone
          DescriptionA cell-permeable, irreversible, broad-spectrum caspase inhibitor (IC50 = 50 nM for caspase-1; IC50 = 100 nM for caspase-8; IC50 = 430 nM for caspase-9; IC50 < 25 nM for caspase-3). Exhibits effective anti-apoptotic properties against all major caspase-mediated cellular apoptosis pathways, including caspase 9/3, caspase 8/10, and caspase 12. Does not exhibit toxic effects even at high concentrations. To reduce hydrophobicity of the peptide and facilitate its use in aqueous media the aspartyl residue is not O-methylated. Shown to reduce ischemic brain damage and stroke-induced programmed cell death in thymus and spleen.
          FormLiquid
          FormulationSupplied as a 10 mM (1 mg/195 µl) solution in DMSO.
          Intert gas (Yes/No) Packaged under inert gas
          Chemical formulaC₂₆H₂₅F₂N₃O₆
          Peptide SequenceQ-Val-Asp-CH₂-OPh
          Structure formulaStructure formula
          Purity≥90% by HPLC
          Storage Protect from light
          -20°C
          Hygroscopic
          Do Not Freeze Ok to freeze
          Special InstructionsFollowing initial thaw, aliquot and freeze (-20°C).
          Toxicity Irritant
          ReferencesBraun, J.S., et al. 2007. Exp. Neurol. 206, 183.
          Caserta, T.M., et al. 2003. Apoptosis 8, 345.
          Rebbaa, A., et al. 2003. Oncogene 22, 2805.
          Citation
        • Braun, J.S., et al. 2007. Exp. Neurol. 206, 183.
        • Jessica H. Dworet and Judy L. Meinkoth. 2006.Molecular Endocrinology 20, 1112.
        • Ademi E. Santiago-Walker, et al. (2005) Protein Kinase C δ Stimulates Apoptosis by Initiating G1 Phase Cell Cycle Progression and S Phase Arrest. Journal of Biological Chemistry 280, 32107-32114.