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539690 Protein Synthesis Initiation Inhibitor, NSC 119889 - Calbiochem

The Protein Synthesis Initiation Inhibitor, NSC 119889 blocks 5'-mediated/cap-dependent initiation of protein synthesis. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.

SDB (Sicherheitsdatenblätter), Analysenzertifikate und Qualitätszertifikate, Dossiers, Broschüren und andere verfügbare Dokumente.

Synonyme: 3,4,5,6-Tetrabromofluorescein

Primary Target: human arginine methyl transferase
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539690
Preis & Verfügbarkeit

Übersicht

Replacement Information

Key Spec Table

Empirical Formula
C₂₀H₈Br₄O₅

Preis & Verfügbarkeit

Bestellnummer VerfügbarkeitVerpackung St./Pkg. Preis Menge
539690-25MG
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      		 Kst.-Ampulle 25 mg
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      Description
      OverviewA cell-permeable, xanthenyl compound that prevents mRNA-ribosome interaction and inhibits 5’-mediated/cap-dependent initiation of protein synthesis (>95% inhibition at 50 µM in in vitro translation assays using Krebs, rabbit reticulocyte, or E. coli S30 extract).
      Catalogue Number539690
      Brand Family Calbiochem®
      Synonyms3,4,5,6-Tetrabromofluorescein
      References
      ReferencesNovac, O., et al. 2004. Nucleic Acids Res. 32, 902.
      Tan, Y.J., et al. 2003. J. Cancer Res. Clin. Oncol. 129, 437.
      Product Information
      ATP CompetitiveN
      FormLight brown solid
      Hill FormulaC₂₀H₈Br₄O₅
      Chemical formulaC₂₀H₈Br₄O₅
      ReversibleN
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary Targethuman arginine methyl transferase
      Primary Target IC<sub>50</sub>1.41 µM against human arginine methyl transferase
      Purity≥95% by HPLC
      Physicochemical Information
      Cell permeableY
      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 Irritant
      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 6 months at -20°C.
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Bestellnummer GTIN
      539690-25MG 04055977194227

      Documentation

      Protein Synthesis Initiation Inhibitor, NSC 119889 - Calbiochem SDB

      Titel

      Sicherheitsdatenblatt (SDB) 

      Protein Synthesis Initiation Inhibitor, NSC 119889 - Calbiochem Analysenzertifikate

      TitelChargennummer
      539690

      Literatur

      Übersicht
      Novac, O., et al. 2004. Nucleic Acids Res. 32, 902.
      Tan, Y.J., et al. 2003. J. Cancer Res. Clin. Oncol. 129, 437.
      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.

      Revision05-September-2007 JSW
      Synonyms3,4,5,6-Tetrabromofluorescein
      DescriptionA cell-permeable, xanthenyl compound that prevents mRNA-ribosome interaction and inhibits 5'-mediated/cap-dependent initiation of protein synthesis (>95% inhibition at 50 µM in in vitro translation assays using Krebs, rabbit reticulocyte, or E. coli S30 extract).
      FormLight brown solid
      Chemical formulaC₂₀H₈Br₄O₅
      Structure formulaStructure formula
      Purity≥95% by HPLC
      SolubilityDMSO (200 mg/ml) or Methanol
      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 6 months at -20°C.
      Toxicity Irritant
      ReferencesNovac, O., et al. 2004. Nucleic Acids Res. 32, 902.
      Tan, Y.J., et al. 2003. J. Cancer Res. Clin. Oncol. 129, 437.