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658425 AG 17 - CAS 10537-47-0 - Calbiochem

Anti-proliferative agent that acts as a selective inhibitor of the platelet-derived growth factor receptor tyrosine kinase (IC₅₀ = 500 nM).

AG 17 - CAS 10537-47-0 - Calbiochem: Ficha de datos de seguridad (MSDS o SDS), certificado de análisis y de calidad (CoA y CoQ), expedientes, folletos y otros documentos disponibles.

Sinónimos: NSC 242557, 3,5-di-t-Butyl-4-hydroxy-benzylidenemalononitrile, α-Cyano-(3,5-di-t-butyl-4-hydroxy)cinnamonitrile, Tyrphostin A9, RG 50872

Primary Target: Platelet-derived growth factor receptor tyrosine kinase
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Descripción

Replacement Information

Tabla espec. clave

CAS #Empirical Formula
10537-47-0C₁₈H₂₂N₂O

Precios y disponibilidad

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658425-5MG
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      Description
      OverviewAnti-proliferative agent that acts as a selective inhibitor of the platelet-derived growth factor receptor tyrosine kinase (IC50 = 500 nM). A potent, cell-permeable, reversible, and substrate competitive inhibitor of TNF-induced tyrosine phosphorylation of PYK2. Uncouples oxidative phosphorylation and induces apoptosis and cell growth arrest in NHL cell lines. Inhibits Cdk2 activity in lymphoma cell lines.
      Catalogue Number658425
      Brand Family Calbiochem®
      SynonymsNSC 242557, 3,5-di-t-Butyl-4-hydroxy-benzylidenemalononitrile, α-Cyano-(3,5-di-t-butyl-4-hydroxy)cinnamonitrile, Tyrphostin A9, RG 50872
      References
      ReferencesFuortes, M., et al. 1999. J. Clin. Invest. 104, 327.
      Palumbo, G.A., et al. 1997. Cancer Res. 57, 2434.
      Burger, A.M., et al. 1995. Cancer Res. 55, 2794.
      Palumbo, G.A., et al. 1994. Blood 84, 296a.
      Bilder, G.E., et al. 1991. Am. J. Physiol. 260, C721.
      Levitzki, A., and Gilon, S. 1991. Trends Pharmacol. Sci. 12, 171.
      Terada, H. 1981. Biochim. Biophys. Acta 639, 225
      Product Information
      CAS number10537-47-0
      ATP CompetitiveY
      FormPale yellow solid
      Hill FormulaC₁₈H₂₂N₂O
      Chemical formulaC₁₈H₂₂N₂O
      ReversibleY
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetPlatelet-derived growth factor receptor tyrosine kinase
      Primary Target IC<sub>50</sub>500 nM against platelet-derived growth factor receptor tyrosine kinase
      Purity≥99% by TLC
      Physicochemical Information
      Cell permeableY
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      RTECSOO3737000
      Safety Information
      R PhraseR: 23/24/25

      Toxic by inhalation, in contact with skin and if swallowed.
      S PhraseS: 36/37/39-45

      Wear suitable protective clothing, gloves and eye/face protection.
      In case of accident or if you feel unwell, seek medical advice immediately (show the label where possible).
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Ambient Temperature Only
      Toxicity Toxic
      Hazardous Materials Attention: Due to the nature of the Hazardous Materials in this shipment, additional shipping charges may be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.
      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
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Número de referencia GTIN
      658425-5MG 04055977261615

      Documentation

      AG 17 - CAS 10537-47-0 - Calbiochem Ficha datos de seguridad (MSDS)

      Título

      Ficha técnica de seguridad del material (MSDS) 

      AG 17 - CAS 10537-47-0 - Calbiochem Certificados de análisis

      CargoNúmero de lote
      658425

      Referencias bibliográficas

      Visión general referencias
      Fuortes, M., et al. 1999. J. Clin. Invest. 104, 327.
      Palumbo, G.A., et al. 1997. Cancer Res. 57, 2434.
      Burger, A.M., et al. 1995. Cancer Res. 55, 2794.
      Palumbo, G.A., et al. 1994. Blood 84, 296a.
      Bilder, G.E., et al. 1991. Am. J. Physiol. 260, C721.
      Levitzki, A., and Gilon, S. 1991. Trends Pharmacol. Sci. 12, 171.
      Terada, H. 1981. Biochim. Biophys. Acta 639, 225

      Folleto

      Cargo
      Caspases and other Apoptosis Related Tools Brochure
      Ficha técnica

      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.

      Revision11-January-2010 RFH
      SynonymsNSC 242557, 3,5-di-t-Butyl-4-hydroxy-benzylidenemalononitrile, α-Cyano-(3,5-di-t-butyl-4-hydroxy)cinnamonitrile, Tyrphostin A9, RG 50872
      DescriptionA selective, cell-permeable, reversible, and substrate competitive inhibitor of the platelet-derived growth factor receptor tyrosine kinase (IC50 = 500 nM). Anti-proliferative agent. Uncoupler of oxidative phosphorylation. Induces apoptosis in vitro and cell growth arrest in NHL cell lines.
      FormPale yellow solid
      CAS number10537-47-0
      RTECSOO3737000
      Chemical formulaC₁₈H₂₂N₂O
      Structure formulaStructure formula
      Purity≥99% by TLC
      SolubilityDMSO (10 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 1 month at -20°C.
      Toxicity Toxic
      ReferencesFuortes, M., et al. 1999. J. Clin. Invest. 104, 327.
      Palumbo, G.A., et al. 1997. Cancer Res. 57, 2434.
      Burger, A.M., et al. 1995. Cancer Res. 55, 2794.
      Palumbo, G.A., et al. 1994. Blood 84, 296a.
      Bilder, G.E., et al. 1991. Am. J. Physiol. 260, C721.
      Levitzki, A., and Gilon, S. 1991. Trends Pharmacol. Sci. 12, 171.
      Terada, H. 1981. Biochim. Biophys. Acta 639, 225