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324623 Eg5 Inhibitor IV, VS-83 - CAS 909250-29-9 - Calbiochem

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CAS #Empirical Formula
909250-29-9C₁₄H₁₁FN₂OS

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324623-5MG
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      Description
      OverviewA cell-permeable Monastrol (Cat. No. 475879) analog with much enhanced potency and selectivity (over 8 other kinesins) in inhibiting mitotic kinesin Eg5-ATPase activity (IC50 = 1.17 vs. 20.73 µM for VS-83 and Monastrol, respectively) and in inducing monoasters formation (EC50 = 7.27 vs. 58.74 µM for BSC-1 cells treated with VS-83 and Monastrol, respectively). Shown to exhibit ≥10-fold antiproliferative activity than Monastrol against U-87 MG, U-118 MG, and U-373 MG glioblastoma cells.
      Catalogue Number324623
      Brand Family Calbiochem®
      Synonyms5-Fluoro-3,4-dihydro-4(3ʹ-hydroxyphenyl)quinazoline-2(1H)-thione
      References
      ReferencesMuller, C., et al. 2007. Cancer Chemother. Pharmacol. 59, 157.
      Santamaria, A., et al. 2007. Mol. Biol. Cell 18, 4024.
      Sarli, V., et al. 2005. ChemBioChem 6, 2005.
      Product Information
      CAS number909250-29-9
      FormWhite solid
      Hill FormulaC₁₄H₁₁FN₂OS
      Chemical formulaC₁₄H₁₁FN₂OS
      Structure formula ImageStructure formula Image
      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 Ambient Temperature Only
      Toxicity Regulatory Review
      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
      Référence GTIN
      324623-5MG 04055977197389

      Documentation

      Eg5 Inhibitor IV, VS-83 - CAS 909250-29-9 - Calbiochem FDS

      Titre

      Fiche de données de sécurité des matériaux (FDS) 

      Références bibliographiques

      Aperçu de la référence bibliographique
      Muller, C., et al. 2007. Cancer Chemother. Pharmacol. 59, 157.
      Santamaria, A., et al. 2007. Mol. Biol. Cell 18, 4024.
      Sarli, V., et al. 2005. ChemBioChem 6, 2005.
      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.

      Revision15-February-2008 JSW
      Synonyms5-Fluoro-3,4-dihydro-4(3ʹ-hydroxyphenyl)quinazoline-2(1H)-thione
      DescriptionA cell-permeable Monastrol (Cat. No. 475879) analog with much enhanced potency and selectivity (over 8 other kinesins) in inhibiting mitotic kinesin Eg5-ATPase activity (IC50 = 1.17 vs. 20.73 µM for VS-83 and Monastrol, respectively) and in inducing monoasters formation (EC50 = 7.27 vs. 58.74 µM for BSC-1 cells treated with VS-83 and Monastrol, respectively). Shown to exhibit ≥10-fold antiproliferative activity than Monastrol against U-87 MG, U-118 MG, and U-373 MG glioblastoma cells.
      FormWhite solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number909250-29-9
      Chemical formulaC₁₄H₁₁FN₂OS
      Structure formulaStructure formula
      Purity≥99% by HPLC
      SolubilityDMSO (50 mg/ml) or Ethanol (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 Regulatory Review
      ReferencesMuller, C., et al. 2007. Cancer Chemother. Pharmacol. 59, 157.
      Santamaria, A., et al. 2007. Mol. Biol. Cell 18, 4024.
      Sarli, V., et al. 2005. ChemBioChem 6, 2005.