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28745 Adenosine 3ʹ,5ʹ-cyclic Monophosphate, N⁶,O2ʹ-Dibutyryl-, Sodium Salt - CAS 16980-89-5 - Calbiochem

This Dibutyryl-cAMP, CAS 16980-89-5, is a cell-permeable cAMP analog that preferentially activates PKA.

Ficha de datos de seguridad (MSDS o SDS), certificado de análisis y de calidad (CoA y CoQ), expedientes, folletos y otros documentos disponibles.

Sinónimos: Dibutyryl-cAMP, Na

Primary Target: PKA
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28745
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Replacement Information

Tabla espec. clave

CAS #Empirical Formula
16980-89-5C₁₈H₂₃N₅O₈P · Na

Precios y disponibilidad

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28745-100MG
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      28745-25MG
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          Description
          OverviewA cell-permeable cAMP analog that preferentially activates cAMP-dependent protein kinase (PKA). Causes an increase in the steady state level of parathyroid hormone-related peptide mRNA. Also acts as a Hh pathway antagonist. Shown to induce apoptosis in vascular smooth muscle cells.
          Catalogue Number28745
          Brand Family Calbiochem®
          SynonymsDibutyryl-cAMP, Na
          References
          ReferencesNoveen, A., et al. 1996. Biochem. Biophys. Res. Commun. 219, 180.
          Tsai, C.H., et al. 1995. J. Cell. Physiol. 164, 108.
          Leszczynski, D., et al. 1994. Am. J. Pathol. 145, 1265.
          Miller, C., et al. 1994. J. Neurosci. Res. 38, 56.
          Hinko, A., and Soloff, M.S. 1993. Endocrinology 132, 126.
          Ikeda, K., et al. 1993. J. Biol. Chem. 268, 1174.
          Park, E.A., et al. 1993. J. Biol. Chem. 268, 613.
          Hei, Y-J., et al. 1991. Mol. Pharmacol. 39, 233.
          Posternak, T., and Weimann, G. 1974. Methods Enzymol. 38, 399.
          Product Information
          CAS number16980-89-5
          ATP CompetitiveN
          FormWhite lyophilized solid
          Hill FormulaC₁₈H₂₃N₅O₈P · Na
          Chemical formulaC₁₈H₂₃N₅O₈P · Na
          Hygroscopic Hygroscopic
          ReversibleN
          Structure formula ImageStructure formula Image
          Quality LevelMQ200
          Applications
          Biological Information
          Primary TargetPKA
          Purity≥95% by HPLC
          Physicochemical Information
          Cell permeableY
          Dimensions
          Materials Information
          Toxicological Information
          Safety Information according to GHS
          RTECSES5055500
          Safety Information
          Product Usage Statements
          Storage and Shipping Information
          Ship Code Ambient Temperature Only
          Toxicity Standard Handling
          Storage -20°C
          Hygroscopic Hygroscopic
          Do not freeze Ok to freeze
          Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C) for long-term storage or refrigerate (4°C) for short-term storage. Aqueous stock solutions are stable for up to 3 days at 4°C or for up to 3 months at -20°C. Avoid pH >8.5.
          Packaging Information
          Transport Information
          Supplemental Information
          Specifications
          Global Trade Item Number
          Número de referencia GTIN
          28745-100MG 04055977197839
          28745-25MG 04055977090970

          Documentation

          Licencias necesarias

          Título
          CARTA DE USO GENERAL 2016
          PRODUCTO REGULADO POR LA SECRETARÍA DE SALUD

          Adenosine 3ʹ,5ʹ-cyclic Monophosphate, N⁶,O2ʹ-Dibutyryl-, Sodium Salt - CAS 16980-89-5 - Calbiochem Ficha datos de seguridad (MSDS)

          Título

          Ficha técnica de seguridad del material (MSDS) 

          Adenosine 3ʹ,5ʹ-cyclic Monophosphate, N⁶,O2ʹ-Dibutyryl-, Sodium Salt - CAS 16980-89-5 - Calbiochem Certificados de análisis

          CargoNúmero de lote
          28745

          Referencias bibliográficas

          Visión general referencias
          Noveen, A., et al. 1996. Biochem. Biophys. Res. Commun. 219, 180.
          Tsai, C.H., et al. 1995. J. Cell. Physiol. 164, 108.
          Leszczynski, D., et al. 1994. Am. J. Pathol. 145, 1265.
          Miller, C., et al. 1994. J. Neurosci. Res. 38, 56.
          Hinko, A., and Soloff, M.S. 1993. Endocrinology 132, 126.
          Ikeda, K., et al. 1993. J. Biol. Chem. 268, 1174.
          Park, E.A., et al. 1993. J. Biol. Chem. 268, 613.
          Hei, Y-J., et al. 1991. Mol. Pharmacol. 39, 233.
          Posternak, T., and Weimann, G. 1974. Methods Enzymol. 38, 399.
          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-March-2008 JSW
          SynonymsDibutyryl-cAMP, Na
          DescriptionCell-permeable cAMP analog that preferentially activates cAMP-dependent protein kinase (PKA). Known to cause an increase in the steady state level of the parathyroid hormone related peptide mRNA. Also acts as a Hh pathway antagonist. Shown to induce apoptosis in vascular smooth muscle cells.
          FormWhite lyophilized solid
          CAS number16980-89-5
          RTECSES5055500
          Chemical formulaC₁₈H₂₃N₅O₈P · Na
          Structure formulaStructure formula
          Purity≥95% by HPLC
          SolubilityH₂O (1 mg/ml)
          Storage -20°C
          Hygroscopic
          Do Not Freeze Ok to freeze
          Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C) for long-term storage or refrigerate (4°C) for short-term storage. Aqueous stock solutions are stable for up to 3 days at 4°C or for up to 3 months at -20°C. Avoid pH >8.5.
          Toxicity Standard Handling
          ReferencesNoveen, A., et al. 1996. Biochem. Biophys. Res. Commun. 219, 180.
          Tsai, C.H., et al. 1995. J. Cell. Physiol. 164, 108.
          Leszczynski, D., et al. 1994. Am. J. Pathol. 145, 1265.
          Miller, C., et al. 1994. J. Neurosci. Res. 38, 56.
          Hinko, A., and Soloff, M.S. 1993. Endocrinology 132, 126.
          Ikeda, K., et al. 1993. J. Biol. Chem. 268, 1174.
          Park, E.A., et al. 1993. J. Biol. Chem. 268, 613.
          Hei, Y-J., et al. 1991. Mol. Pharmacol. 39, 233.
          Posternak, T., and Weimann, G. 1974. Methods Enzymol. 38, 399.