Millipore Sigma Vibrant Logo

115500 Adenophostin A, Hexasodium Salt - Calbiochem

Adenophostin A, Hexasodium Salt, is a potent agonist of type 1 inositol 1,4,5-trisphosphate receptor (InsP3R; EC50 = 10.9 nM). Exhibits about 50- to 100-fold greater affinity for IP3R than IP3.

Adenophostin A, Hexasodium Salt - Calbiochem: Ficha de datos de seguridad (MSDS o SDS), certificado de análisis y de calidad (CoA y CoQ), expedientes, folletos y otros documentos disponibles.
Primary Target: Type 1 inositol 1,4,5-trisphosphate receptor (InsP3R)
View Products on Sigmaaldrich.com
115500
Ver precios y disponibilidad

Descripción

Replacement Information

Tabla espec. clave

Empirical Formula
C₁₆H₂₀N₅O₁₈P₃ · 6Na

Precios y disponibilidad

Número de referencia DisponiblidadEmbalaje Cant./Env. Precio Cantidad
115500-50UG
Comprobando disponibilidad...
—
Disponibilidad a confirmar Disponibilidad a confirmar
Ingrese cantidad 
Suspendido
Cantidades limitadas disponibles
Debe confirmarse disponibilidad
    El resto: se avisará
      El resto: se avisará
      Se avisará
      Póngase en contacto con el Servicio de Atención al Cliente
      Contact Customer Service

      		 50 μg
      Recuperando precio...
      No pudo obtenerse el precio
      La cantidad mínima tiene que ser múltiplo de
      Maximum Quantity is
      Al finalizar el pedido Más información
      Ahorró ()
       
      —
      Solicitar precio
      		 —
      Description
      OverviewOne of the most potent known agonist of type 1 inositol 1,4,5-trisphosphate receptor (InsP3R; EC50 = 10.9 nM). Exhibits about 50- to 100-fold greater affinity for IP3R than IP3. Stimulates Ca2+ release from Ins(1,4,5)P3-sensitive Ca2+ stores in microsomal preparations, permeabilized cells, and lipid vesicles containing purified InsP3R (EC50 = 14.7 nM for Ca2+ release from permeabilized hepatocytes). Does not bind to Ins(1,3,4,5)P4 binding sites and is resistant to enzymatic degradation.
      Catalogue Number115500
      Brand Family Calbiochem®
      References
      ReferencesCorrea, V., et al. 2001. Mol. Pharmacol. 59, 1206.
      Marchant, J.S., and Taylor, C.W. 1998. Biochemistry 37, 11524.
      DeLisle, S., et al. 1997. J. Biol. Chem. 272, 9956.
      Hartzell, H.C., et al. 1997. Mol. Pharmacol. 51, 683.
      Marchant, J.S., et al. 1997. Biochemistry 36, 12780.
      Hirota, J., et al. 1995. FEBS Lett. 368, 248.
      Takahashi, M., et al. 1994. J. Biol. Chem. 269, 369.
      Product Information
      ATP CompetitiveN
      FormWhite solid
      Hill FormulaC₁₆H₂₀N₅O₁₈P₃ · 6Na
      Chemical formulaC₁₆H₂₀N₅O₁₈P₃ · 6Na
      Hygroscopic Hygroscopic
      ReversibleN
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      ApplicationAdenophostin A, Hexasodium Salt, is a potent agonist of type 1 inositol 1,4,5-trisphosphate receptor (InsP3R; EC50 = 10.9 nM). Exhibits about 50- to 100-fold greater affinity for IP3R than IP3.
      Biological Information
      Primary TargetType 1 inositol 1,4,5-trisphosphate receptor (InsP3R)
      Primary Target IC<sub>50</sub>EC50 = 10.9 nM against InsP3R
      Purity≥90% by HPLC
      Physicochemical Information
      Cell permeableN
      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
      Hygroscopic Hygroscopic
      Do not freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable up to 3 months at -20°C.
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Número de referencia GTIN
      115500-50UG 07790788060244

      Documentation

      Licencias necesarias

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

      Adenophostin A, Hexasodium Salt - Calbiochem Ficha datos de seguridad (MSDS)

      Título

      Ficha técnica de seguridad del material (MSDS) 

      Adenophostin A, Hexasodium Salt - Calbiochem Certificados de análisis

      CargoNúmero de lote
      115500

      Referencias bibliográficas

      Visión general referencias
      Correa, V., et al. 2001. Mol. Pharmacol. 59, 1206.
      Marchant, J.S., and Taylor, C.W. 1998. Biochemistry 37, 11524.
      DeLisle, S., et al. 1997. J. Biol. Chem. 272, 9956.
      Hartzell, H.C., et al. 1997. Mol. Pharmacol. 51, 683.
      Marchant, J.S., et al. 1997. Biochemistry 36, 12780.
      Hirota, J., et al. 1995. FEBS Lett. 368, 248.
      Takahashi, M., et al. 1994. J. Biol. Chem. 269, 369.

      Folleto

      Cargo
      Inorganics & Solvents for classical analysis
      Safety Connects - Solvents Withdrawal System 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.

      Revision07-April-2008 RFH
      DescriptionA glyconucleotide originally isolated from the culture broth of Penicillium brevicompactum. Adenophostin A is the most potent known agonist of type 1 inositol 1,4,5-trisphosphate receptor (InsP3R). Exhibits about 50-100 fold greater affinity for the InsP3R than IP3. Stimulates Ca2+ release from Ins(1,4,5)P3-sensitive Ca2+ stores in microsomal preparations, permeabilized cells, and lipid vesicles containing purified InsP3R. Does not bind to Ins(1,3,4,5)P4 binding sites and is resistant to degradation by the enzymes that metabolize (1,4,5)InsP3.
      FormWhite solid
      Chemical formulaC₁₆H₂₀N₅O₁₈P₃ · 6Na
      Structure formulaStructure formula
      Purity≥90% by HPLC
      SolubilityH₂O (1 mg/ml)
      Storage -20°C
      Hygroscopic
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable up to 3 months at -20°C.
      Toxicity Standard Handling
      ReferencesCorrea, V., et al. 2001. Mol. Pharmacol. 59, 1206.
      Marchant, J.S., and Taylor, C.W. 1998. Biochemistry 37, 11524.
      DeLisle, S., et al. 1997. J. Biol. Chem. 272, 9956.
      Hartzell, H.C., et al. 1997. Mol. Pharmacol. 51, 683.
      Marchant, J.S., et al. 1997. Biochemistry 36, 12780.
      Hirota, J., et al. 1995. FEBS Lett. 368, 248.
      Takahashi, M., et al. 1994. J. Biol. Chem. 269, 369.

      Productos y aplicaciones relacionados

      Accessories (Primary)

      Número de referencia Descripción  
      101114 Sistema de toma Precios y disponibilidad
      106710 Sistema de toma para barriles y tambores de acero inoxidable Precios y disponibilidad
      108803 Llave para tambores Precios y disponibilidad
      902698 Seguro contra sobrepresión 0,5 bar Precios y disponibilidad
      963533 Recipiente de transporte de seguridad Precios y disponibilidad
      964205 Descompresor, 0,2 bar con 2 empalmes de tubos 6 x 8 mm y seguro integrado contra hipertensión 0,5 bar Precios y disponibilidad

      Accessories (Secondary)

      Número de referencia Descripción  
      100801 Juego de etiquetas según GHS Precios y disponibilidad
      107070 Dispositivo antiestático Precios y disponibilidad
      108801 Llave para frascos Precios y disponibilidad
      119171 Sistema de toma para disolventes Precios y disponibilidad

      Categorías

      Life Science Research > Inhibitors and Biochemicals > Small Molecules & Inhibitors > Calcium Signaling > IP3 and Ryanodine Channel Modulators