Millipore Sigma Vibrant Logo
Attention: We have moved. Merck Millipore products are no longer available for purchase on MerckMillipore.com.Learn More

116818 Adenosine 3ʹ,5ʹ-cyclic Monophosphorothioate, 8-Bromo-, Sp-Isomer, Sodium Salt - Calbiochem

A potent cell-permeable, metabolically-stable activator of cAMP-dependent protein kinase (PKA).

MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

Synonyms: Sp-8-Br-cAMPS, Na

Primary Target: PKA
View Products on Sigmaaldrich.com
116818
  
Purchase on Sigma-Aldrich

Overview

Replacement Information

Key Spec Table

Empirical Formula
C₁₀H₁₀BrN₅O₅PS · Na
Description
Overview

This product has been discontinued.



A potent cell-permeable, metabolically-stable activator of cAMP-dependent protein kinase (PKA). Induces guanine nucleotide exchange factor activity of GEFI (also known as Epac) and GEFII towards Rap1 both in vivo and in vitro. Significantly more lipophilic and cell-permeable than Sp-cAMPS (Cat. No. 116815). Note: 5 µmol = 2.23 mg.
Catalogue Number116818
Brand Family Calbiochem®
SynonymsSp-8-Br-cAMPS, Na
References
ReferencesKawasaki, H., et al. 1998. Science 282, 2275.
de Rooij, J., et al. 1998. Nature 396, 474.
Holen, I., et al. 1996. Eur. J. Biochem. 236, 163.
Schaap, P., et al. 1993. J. Biol. Chem. 268, 6323.
Yokozaki, H., et al. 1992. Cancer Res. 52, 2504.
Product Information
ATP CompetitiveN
DeclarationSold under license of Patent DE 3,802,865.4 issued to BIOLOG LSI.
FormLyophilized
Hill FormulaC₁₀H₁₀BrN₅O₅PS · Na
Chemical formulaC₁₀H₁₀BrN₅O₅PS · Na
Hygroscopic Hygroscopic
ReversibleN
Structure formula ImageStructure formula Image
Quality LevelMQ100
Applications
Biological Information
Primary TargetPKA
Purity≥99% 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
Hygroscopic Hygroscopic
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
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Catalogue Number GTIN
116818 0

Documentation

Adenosine 3ʹ,5ʹ-cyclic Monophosphorothioate, 8-Bromo-, Sp-Isomer, Sodium Salt - Calbiochem SDS

Title

Safety Data Sheet (SDS) 

Adenosine 3ʹ,5ʹ-cyclic Monophosphorothioate, 8-Bromo-, Sp-Isomer, Sodium Salt - Calbiochem Certificates of Analysis

TitleLot Number
116818

References

Reference overview
Kawasaki, H., et al. 1998. Science 282, 2275.
de Rooij, J., et al. 1998. Nature 396, 474.
Holen, I., et al. 1996. Eur. J. Biochem. 236, 163.
Schaap, P., et al. 1993. J. Biol. Chem. 268, 6323.
Yokozaki, H., et al. 1992. Cancer Res. 52, 2504.
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.

Revision26-September-2007 RFH
SynonymsSp-8-Br-cAMPS, Na
DescriptionA potent cell-permeable, metabolically stable activator of cAMP-dependent protein kinase (PKA). Induces the guanine-nucleotide-exchange factor activity of GEFI, also known as Epac (exchange protein directly activated by cAMP), and GEFII towards Rap1 both in vivo and in vitro. Significantly more lipophilic and cell permeable than Sp-cAMPS (Cat. No. 116815). λmax = 264 nm (H2O, pH 7.0); εmax = 17,000 M-1cm-1. Note: 5 µmol = 2.23 mg.
FormLyophilized
Chemical formulaC₁₀H₁₀BrN₅O₅PS · Na
Structure formulaStructure formula
Purity≥99% by HPLC
SolubilityH₂O (40 mg/ml)
Storage -20°C
Hygroscopic
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
ReferencesKawasaki, H., et al. 1998. Science 282, 2275.
de Rooij, J., et al. 1998. Nature 396, 474.
Holen, I., et al. 1996. Eur. J. Biochem. 236, 163.
Schaap, P., et al. 1993. J. Biol. Chem. 268, 6323.
Yokozaki, H., et al. 1992. Cancer Res. 52, 2504.