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505308 CDDO-Me - CAS 218600-53-4 - Calbiochem

CDDO-Me - CAS 218600-53-4 - 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: Bardoxolone methyl, BARD, NSC 713200, Methyl-2-cyano-3,12-dioxooleana-1,9(11)-dien-28-oate, Nrf Activator V

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      Descripción

      Replacement Information

      Tabla espec. clave

      CAS #Empirical Formula
      218600-53-4C₃₂H₄₃NO₄
      Description
      OverviewA cell-permeable, bioavailable synthetic oleanane triterpenoid compound with anti-inflammatory, anti-tumor and cytoprotective properties. Shown to significantly reduce the expression of several inflammatory mediators, including IL-6, IL-10, IL-12, TNFα, Mip1α and others. Reverses high fat diet-induced type 2 diabetes in C57BL/6 mice (3 mg/kg) and improves glucose homeostasis and insulin sensitivity. Down-regulates lipogenic gene expression in hepatocytes. Exhibits anti-proliferative activity in osteosarcoma cells (IC50 = 800, 150, 330, and 170 nM in HOB-c, KHOS, KHOSR2, and U2OS cells, respectively). Enhances the effectiveness of chemotherapeutic agents by inducing intrinsic mitochondrial-dependent apoptotic pathway. Reported to interact with multi cellular targets, namely, Nrf2-Keap1, IKK, JAK-STAT, PPARγ, ErbB2, PTEN, mTOR and Arp3 and covalently modify active site Cys residue via Michael addition.
      Catalogue Number505308
      Brand Family Calbiochem®
      SynonymsBardoxolone methyl, BARD, NSC 713200, Methyl-2-cyano-3,12-dioxooleana-1,9(11)-dien-28-oate, Nrf Activator V
      References
      ReferencesLiby, K.T. and Sporn, M.B., 2012. Pharmacol. Rev. 64, 972.
      Saha, P.K. et al. 2010. J. Biol. Chem. 285, 40581.
      Ryu, K., et al. 2010. BMC Cancer 10, 187.
      Liby, K.T., et al. 2007. Nat. Rev. Cancer 7, 357.
      Shishodia S., et al. 2006. Clin. Cancer Res. 12, 1828.
      Zou, W., et al. 2004. Cancer Res. 64, 7570.
      Kim, Y., et al. 2002. J. Biol. Chem. 277, 22320.
      Konopleva, M., et al. 2002. Blood 99, 326.
      Wang, Y., et al. 2000. Mol Endocrinol. 14, 1550.
      Product Information
      CAS number218600-53-4
      FormWhite solid
      Hill FormulaC₃₂H₄₃NO₄
      Chemical formulaC₃₂H₄₃NO₄
      ReversibleN
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Purity≥98% 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 +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
      Packaged under inert gas Packaged under inert gas
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Número de referencia GTIN
      505308 0

      Documentation

      CDDO-Me - CAS 218600-53-4 - Calbiochem Ficha datos de seguridad (MSDS)

      Título

      Ficha técnica de seguridad del material (MSDS) 

      Referencias bibliográficas

      Visión general referencias
      Liby, K.T. and Sporn, M.B., 2012. Pharmacol. Rev. 64, 972.
      Saha, P.K. et al. 2010. J. Biol. Chem. 285, 40581.
      Ryu, K., et al. 2010. BMC Cancer 10, 187.
      Liby, K.T., et al. 2007. Nat. Rev. Cancer 7, 357.
      Shishodia S., et al. 2006. Clin. Cancer Res. 12, 1828.
      Zou, W., et al. 2004. Cancer Res. 64, 7570.
      Kim, Y., et al. 2002. J. Biol. Chem. 277, 22320.
      Konopleva, M., et al. 2002. Blood 99, 326.
      Wang, Y., et al. 2000. Mol Endocrinol. 14, 1550.
      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.

      Revision26-July-2013 JSW
      SynonymsBardoxolone methyl, BARD, NSC 713200, Methyl-2-cyano-3,12-dioxooleana-1,9(11)-dien-28-oate, Nrf Activator V
      DescriptionA cell-permeable, bioavailable synthetic oleanane triterpenoid compound with anti-inflammatory, anti-tumor and cytoprotective properties. Shown to significantly reduce the expression of several inflammatory mediators, including IL-6, IL-10, IL-12, TNFα, Mip1α and others. Reverses high fat diet-induced type 2 diabetes in C57BL/6 mice (3 mg/kg) and improves glucose homeostasis and insulin sensitivity. Down-regulates lipogenic gene expression in hepatocytes. Exhibits anti-proliferative activity in osteosarcoma cells (IC50 = 800, 150, 330, and 170 nM in HOB-c, KHOS, KHOSR2, and U2OS cells, respectively). Enhances the effectiveness of chemotherapeutic agents by inducing intrinsic mitochondrial-dependent apoptotic pathway. Reported to interact with multi cellular targets, namely, Nrf2-Keap1, IKK, JAK-STAT, PPARγ, ErbB2, PTEN, mTOR and Arp3 and covalently modify active site Cys residue via Michael addition.
      FormWhite solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number218600-53-4
      Chemical formulaC₃₂H₄₃NO₄
      Structure formulaStructure formula
      Purity≥98% by HPLC
      SolubilityDMSO (50 mg/ml). Use only fresh DMSO for reconstitution.
      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 Standard Handling
      ReferencesLiby, K.T. and Sporn, M.B., 2012. Pharmacol. Rev. 64, 972.
      Saha, P.K. et al. 2010. J. Biol. Chem. 285, 40581.
      Ryu, K., et al. 2010. BMC Cancer 10, 187.
      Liby, K.T., et al. 2007. Nat. Rev. Cancer 7, 357.
      Shishodia S., et al. 2006. Clin. Cancer Res. 12, 1828.
      Zou, W., et al. 2004. Cancer Res. 64, 7570.
      Kim, Y., et al. 2002. J. Biol. Chem. 277, 22320.
      Konopleva, M., et al. 2002. Blood 99, 326.
      Wang, Y., et al. 2000. Mol Endocrinol. 14, 1550.