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352010 Glutaminase Inhibitor, Compound 968 - CAS 311795-38-7 - Calbiochem

Übersicht

Replacement Information

Key Spec Table

CAS #Empirical Formula
311795-38-7C₂₇H₂₇BrN₂O

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352010-10MG
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      Glasflasche 10 mg
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      Description
      OverviewA cell-permeable benzophenanthridinone compound that acts as an allosteric and reversible inhibitor of mitochondrial glutaminase activity and represses the growth and invasive activity in glutaminase upregulated fibroblasts and in tumor cells (IC50 ≤ 10 µM in NIH3T3 cells stably expressing Dbl, Cdc42-F28L, Rac-F28L or RhoC-F30L mutants and in SKBR3 and MDA-MB231 cancer cells). Shown to effectively shrink tumor size in P-493 B xenografted mouse model (200 µg per inj. i.p., 12 days). Also available as a 10 mM solution in DMSO (Cat. No. 506073).
      Catalogue Number352010
      Brand Family Calbiochem®
      Synonyms5-(3-Bromo-4-(dimethylamino)phenyl)-2,2-dimethyl-2,3,5,6-tetrahydrobenzo[a]phenanthridin-4(1H)-one, GAC Inhibitor, GLS1 Inhibitor I, KGA Inhibitor I, Kidney-Type Glutaminase Inhibitor I
      References
      ReferencesWang, J.B., et al. 2010. Cancer Cell 18, 207.
      Product Information
      CAS number311795-38-7
      FormWhite powder
      Hill FormulaC₂₇H₂₇BrN₂O
      Chemical formulaC₂₇H₂₇BrN₂O
      Quality LevelMQ100
      Applications
      Biological Information
      Purity≥99% by HPLC
      Physicochemical Information
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
      Toxicity Standard Handling
      Storage -20°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 3 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
      352010-10MG 04055977193237

      Documentation

      Glutaminase Inhibitor, Compound 968 - CAS 311795-38-7 - Calbiochem SDB

      Titel

      Sicherheitsdatenblatt (SDB) 

      Glutaminase Inhibitor, Compound 968 - CAS 311795-38-7 - Calbiochem Analysenzertifikate

      TitelChargennummer
      352010

      Literatur

      Übersicht
      Wang, J.B., et al. 2010. Cancer Cell 18, 207.
      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.

      Revision10-August-2012 JSW
      Synonyms5-(3-Bromo-4-(dimethylamino)phenyl)-2,2-dimethyl-2,3,5,6-tetrahydrobenzo[a]phenanthridin-4(1H)-one, GAC Inhibitor, GLS1 Inhibitor I, KGA Inhibitor I, Kidney-Type Glutaminase Inhibitor I
      DescriptionA cell-permeable benzophenanthridinone compound that acts as an allosteric and reversible inhibitor of mitochondrial glutaminase activity and represses the growth and invasive activity in glutaminase upregulated fibroblasts and in tumor cells (IC50 ≤ 10 µM in NIH3T3 cells stably expressing Dbl, Cdc42-F28L, Rac-F28L or RhoC-F30L mutants and in SKBR3 and MDA-MB231 cancer cells). Shown to effectively shrink tumor size in P-493 B xenografted mouse model (200 µg per inj. i.p., 12 days).
      FormWhite powder
      Intert gas (Yes/No) Packaged under inert gas
      CAS number311795-38-7
      Chemical formulaC₂₇H₂₇BrN₂O
      Purity≥99% by HPLC
      SolubilityDMSO (5 mg/ml)
      Storage Protect from light
      -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
      ReferencesWang, J.B., et al. 2010. Cancer Cell 18, 207.