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475846 MIF Antagonist III, 4-IPP - CAS 41270-96-6 - Calbiochem

Übersicht

Replacement Information

Key Spec Table

CAS #Empirical Formula
41270-96-6C₁₀H₇IN₂

Preis & Verfügbarkeit

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475846-10MG
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      Glasflasche 10 mg
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      Description
      OverviewA cell-permeable iodo-pyrimidine compound that covalently modifies MIF N-terminal proline and exhibits higher MIF inhibitory potency than ISO-1 (Cat. No. 475837) in cell-free dopachrome tautomerase activity assays (IC50 ~5 vs. 50 µM, respectively, using recombinant human MIF) as well as in cell-based migration assays (50% vs 0% inhibition with respective inhibitor at 10 µM) and anchorage-independent growth (57% vs 0% inhibition with respective inhibitor at 10 µM) using human lung adenocarcinoma A549. Also shown to reduce A549 cellular active Rac1 population (50 µM, 16 h) in vitro and effectively decrease liver tautomerase activity by 50% in mice (1 mg/animal/day or ~50 mg/kg/day via i.p.) in vivo.
      Catalogue Number475846
      Brand Family Calbiochem®
      SynonymsMacrophage Migration Inhibitory Factor Antagonist III, 4-IPP, 4-Iodo-6-phenylpyrimidine
      References
      ReferencesWinner, M., et al. 2008. Cancer Res. 68, 7253.
      Product Information
      CAS number41270-96-6
      FormAmber solid
      Hill FormulaC₁₀H₇IN₂
      Chemical formulaC₁₀H₇IN₂
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Purity≥90% 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 +2°C to +8°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
      475846-10MG 04055977185010

      Documentation

      MIF Antagonist III, 4-IPP - CAS 41270-96-6 - Calbiochem SDB

      Titel

      Sicherheitsdatenblatt (SDB) 

      MIF Antagonist III, 4-IPP - CAS 41270-96-6 - Calbiochem Analysenzertifikate

      TitelChargennummer
      475846

      Literatur

      Übersicht
      Winner, M., et al. 2008. Cancer Res. 68, 7253.
      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.

      Revision14-March-2011 RFH
      SynonymsMacrophage Migration Inhibitory Factor Antagonist III, 4-IPP, 4-Iodo-6-phenylpyrimidine
      DescriptionA cell-permeable iodo-pyrimidine compound that covalently modifies MIF N-terminal proline and exhibits higher MIF inhibitory potency than ISO-1 (Cat. No. 475837) in cell-free dopachrome tautomerase activity assays (IC50 ~5 vs. 50 µM, respectively, using recombinant human MIF) as well as in cell-based migration assays (50% vs 0% inhibition with respective inhibitor at 10 µM) and anchorage-independent growth (57% vs 0% inhibition with respective inhibitor at 10 µM) using human lung adenocarcinoma A549. Also shown to reduce A549 cellular active Rac1 population (50 µM, 16 h) in vitro and effectively decrease liver tautomerase activity by 50% in mice (1 mg/animal/day or ~50 mg/kg/day via i.p.) in vivo.
      FormAmber solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number41270-96-6
      Chemical formulaC₁₀H₇IN₂
      Structure formulaStructure formula
      Purity≥90% by HPLC
      SolubilityDMSO (50 mg/ml)
      Storage Protect from light
      +2°C to +8°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
      ReferencesWinner, M., et al. 2008. Cancer Res. 68, 7253.