251650 Damnacanthal - CAS 477-84-9 - Calbiochem

251650
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Empirical FormulaCAS #
C₁₆H₁₀O₅ 477-84-9

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251650-1MGCN
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      Plastic ampoule 1 mg
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      Description
      OverviewA cell-permeable, potent, reversible, and selective inhibitor of p56lck tyrosine kinase. Inhibits p56lck autophosphorylation (IC50 = 17 nM) and phosphorylation of an exogenous peptide by p56lck (IC50 = 620 nM). Exhibits over 100-fold greater selectivity for p56lck over PKA and PKC, 40-fold greater selectivity for p56lck over EGF receptor kinase, c-ErbB2, insulin receptor kinase, and PDGF receptor kinase, and 7 - 20-fold greater selectivity for p56lck over p60src and p59fyn. Inhibition of p56lck is not significantly affected by the presence of sulfhydryl reagents. Also known to have antimalarial properties and to reverse the phenotype of ras-transformed cells.
      Catalogue Number251650
      Brand Family Calbiochem®
      Synonyms3-Hydroxy-1-methoxyanthraquinone-2-aldehyde
      References
      ReferencesFaltynek, C.R., et al. 1995. Biochemistry 34, 12404.
      Hiramatsu, T., et al. 1993. Cancer Lett. 73, 161.
      Koumaglo, K., et al. 1992. Planta Med. 58, 533.
      Product Information
      CAS number477-84-9
      ATP CompetitiveN
      FormOrange-yellow solid
      Hill FormulaC₁₆H₁₀O₅
      Chemical formulaC₁₆H₁₀O₅
      ReversibleY
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary Targetp56lck autophosphorylation
      Primary Target IC<sub>50</sub>17 nM against p56lck autophosphorylation
      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 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 1 month at -20°C.
      Packaging Information
      Packaged under inert gas Packaged under inert gas
      Transport Information
      Supplemental Information
      Specifications

      Documentation

      Damnacanthal - CAS 477-84-9 - Calbiochem MSDS

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      물질안전보건자료(MSDS) 

      Damnacanthal - CAS 477-84-9 - Calbiochem Certificates of Analysis

      TitleLot Number
      251650

      References

      참고문헌 보기
      Faltynek, C.R., et al. 1995. Biochemistry 34, 12404.
      Hiramatsu, T., et al. 1993. Cancer Lett. 73, 161.
      Koumaglo, K., et al. 1992. Planta Med. 58, 533.
      Data Sheet

      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.

      Revision21-April-2011 JSW
      Synonyms3-Hydroxy-1-methoxyanthraquinone-2-aldehyde
      DescriptionA cell-permeable, potent, reversible, and selective inhibitor of p56lck tyrosine kinase activity. Inhibits p56lck autophosphorylation (IC50 = 17 nM) and phosphorylation of an exogenous peptide by p56lck over PKA and PKC and >40 fold selectivity for p56lck over EGF, c-erbB2, insulin, and the PDGF receptor tyrosine kinases. In addition, damnacanthal exhibits 7-20 fold selectivity for p56lck over pp60src and pp59fyn. Inhibition of p56lck by damnacanthal appears to be reversible, not time-dependent and not significantly affected by the presence of sulfhydryl reagents. Also known to have antimalarial properties, and to reverse the phenotype of ras-transformed cells.
      FormOrange-yellow solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number477-84-9
      Chemical formulaC₁₆H₁₀O₅
      Structure formulaStructure formula
      Purity≥95% by HPLC
      SolubilityDMSO (5 mg/ml)
      Storage -20°C
      Protect from light
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 1 month at -20°C.
      Toxicity Standard Handling
      ReferencesFaltynek, C.R., et al. 1995. Biochemistry 34, 12404.
      Hiramatsu, T., et al. 1993. Cancer Lett. 73, 161.
      Koumaglo, K., et al. 1992. Planta Med. 58, 533.