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219007 Caspase Inhibitor VI - CAS 161401-82-7 - Calbiochem

Übersicht

Replacement Information

Key Spec Table

CAS #Empirical Formula
161401-82-7C₂₁H₂₈FN₃O₇

Preis & Verfügbarkeit

Bestellnummer VerfügbarkeitVerpackung St./Pkg. Preis Menge
219007-1MG
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      Kst.-Ampulle 1 mg
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      219007-250UG
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      Eingeschränkte Verfügbarkeit
Eingeschränkte Verfügbarkeit
      Lieferbar 
      Produkt wurde eingestellt
      Begrenzter Lagerbestand
      Bestätigung der Verfügbarkeit erforderlich
        Restmenge: Angebot folgt
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          Contact Customer Service

          Kst.-Ampulle 250 μg
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          Die Mindestmenge muss ein Vielfaches sein von
          Maximum Quantity is
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          Description
          OverviewAn irreversible general caspase inhibitor. Useful for studies involving recombinant, isolated, and purified caspase enzymes. Unlike Caspase Inhibitor I (Cat. No. 627610), this inhibitor does not require pretreatment with esterase for in vitro studies. A 10 mM (1 mg/221 µl) solution of Caspase Inhibitor VI (Cat. No. 219011) in DMSO is also available.
          Catalogue Number219007
          Brand Family Calbiochem®
          SynonymsZ-VAD-FMK
          References
          ReferencesMisaghi, S., et al. 2004. Chem. Biol. 11, 1677.
          Product Information
          CAS number161401-82-7
          ATP CompetitiveN
          FormOff-white solid
          Hill FormulaC₂₁H₂₈FN₃O₇
          Chemical formulaC₂₁H₂₈FN₃O₇
          ReversibleN
          Structure formula ImageStructure formula Image
          Quality LevelMQ100
          Applications
          Biological Information
          Primary Targetgeneral caspase inhibitor
          Purity≥98% by HPLC
          Physicochemical Information
          Cell permeableN
          Peptide SequenceZ-Val-Ala-Asp-CH₂F*
          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 -20°C
          Protect from Moisture Protect from moisture
          Do not freeze Ok to freeze
          Special InstructionsFollowing reconstitution aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
          Packaging Information
          Transport Information
          Supplemental Information
          Specifications
          Global Trade Item Number
          Bestellnummer GTIN
          219007-1MG 07790788048648
          219007-250UG 04055977202021

          Documentation

          Caspase Inhibitor VI - CAS 161401-82-7 - Calbiochem SDB

          Titel

          Sicherheitsdatenblatt (SDB) 

          Caspase Inhibitor VI - CAS 161401-82-7 - Calbiochem Analysenzertifikate

          TitelChargennummer
          219007

          Literatur

          Übersicht
          Misaghi, S., et al. 2004. Chem. Biol. 11, 1677.

          Broschüre

          Titel
          Caspases and other Apoptosis Related Tools Brochure

          Literaturstellen

          Titel
        • Liwei Chen, et al. (2005) Chemical ablation of androgen receptor in prostate cancer cells by the histone deacetylase inhibitor LAQ824. Molecular Cancer Therapeutics 4, 1311-1319.
        • Heui-Young Ryu, et al. (2005) Environmental Chemical-Induced Bone Marrow B Cell Apoptosis: Death Receptor-Independent Activation of a Caspase-3 to Caspase-8 Pathway. Molecular Pharmacology 68, 1087-1096.
        • Yumin Zhang, et al. (2004) Peroxynitrite-Induced Neuronal Apoptosis is Mediated by Intracellular Zinc Release and 12-Lipoxygenase Activation. Journal of Neuroscience 24, 10616-10627.
        • Dong Zhang, et al. (2001) Granzymes A and B Directly Cleave Lamins and Disrupt the Nuclear Lamina During Granule-Mediated Cytolysis. Proceedings of the National Academy of Science USA 98, 5746-5751.
        • Brian L. Webb, Elsa Jimenez and G. Steven Martin. (2000) v-Src Generates a p53-Independent Apoptotic Signal. Molecular and Cellular Biology 20, 9271-9280.
        • 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.

          Revision17-July-2014 JSW
          SynonymsZ-VAD-FMK
          DescriptionA cell-permeable, irreversible, and general caspase inhibitor. Also reported to inhibit Peptide: N-glycanase (PNGase) in vitro and in vivo. Useful for studies involving recombinant, isolated, and purified caspase enzymes. Unlike Caspase Inhibitor I (Cat. No. 627610), this inhibitor does not require pretreatment with esterase for in vitro studies.
          FormOff-white solid
          CAS number161401-82-7
          Chemical formulaC₂₁H₂₈FN₃O₇
          Peptide SequenceZ-Val-Ala-Asp-CH₂F*
          Structure formulaStructure formula
          Purity≥98% by HPLC
          SolubilityDMSO (9 mg/ml)
          Storage Protect from moisture
          -20°C
          Do Not Freeze Ok to freeze
          Special InstructionsFollowing reconstitution aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
          Toxicity Standard Handling
          ReferencesMisaghi, S., et al. 2004. Chem. Biol. 11, 1677.
          Citation
        • Liwei Chen, et al. (2005) Chemical ablation of androgen receptor in prostate cancer cells by the histone deacetylase inhibitor LAQ824. Molecular Cancer Therapeutics 4, 1311-1319.
        • Heui-Young Ryu, et al. (2005) Environmental Chemical-Induced Bone Marrow B Cell Apoptosis: Death Receptor-Independent Activation of a Caspase-3 to Caspase-8 Pathway. Molecular Pharmacology 68, 1087-1096.
        • Yumin Zhang, et al. (2004) Peroxynitrite-Induced Neuronal Apoptosis is Mediated by Intracellular Zinc Release and 12-Lipoxygenase Activation. Journal of Neuroscience 24, 10616-10627.
        • Dong Zhang, et al. (2001) Granzymes A and B Directly Cleave Lamins and Disrupt the Nuclear Lamina During Granule-Mediated Cytolysis. Proceedings of the National Academy of Science USA 98, 5746-5751.
        • Brian L. Webb, Elsa Jimenez and G. Steven Martin. (2000) v-Src Generates a p53-Independent Apoptotic Signal. Molecular and Cellular Biology 20, 9271-9280.