Product Description:
Adenosine-5''-O-(1-thiotriphosphate), Sp-isomer is a chiral analog of ATP often used in studies of nucleotide-binding proteins and kinases.
Applications & Uses:
CAS#:
162177-27-9
SYNONYM:
ATP-alpha-S;Adenosine 5'-(1-thiotriphosphate), Sp isomer
FORMULA:
C10H16N5O12P3S
PRODUCT TYPE:
HAZARD:
CATEGORIES:
Research and Development
,
Specialty Chemicals
Technical Specifications
Molecular weight, g/mol :
554.24
Introducing Adenosine-5''-O-(1-thiotriphosphate), Sp-isomer, a high-purity nucleotide analog designed for advanced biochemical research and applications. This compound is a chemically synthesized analog of ATP, where the oxygen in the triphosphate group is replaced with a sulfur atom, providing unique properties for specialized applications. Known for its exceptional stability and reactivity, the Sp-isomer is crucial for studying ATP-dependent processes and enzyme mechanisms with increased resistance to cleavage by phosphatases, making it an indispensable tool in molecular biology and biochemistry laboratories.
Suited for use in a variety of experimental setups, Adenosine-5''-O-(1-thiotriphosphate), Sp-isomer is ideal for investigating intricate enzymatic pathways, signaling cascades, and interactions involving nucleotide-binding proteins. Its role as a non-hydrolyzable ATP analog enables precise control in studies of kinase activities, receptor activation, and membrane transport systems. Additionally, this compound serves as a valuable component in structure-function studies of ATP-binding proteins, providing insights into the energetics and mechanics of ATP-induced conformational changes.
With its distinct sulfhydryl substitution, Adenosine-5''-O-(1-thiotriphosphate), Sp-isomer also functions as an inhibitor for enzymatic reactions that require ATP, offering researchers the capability to dissect the subtleties of ATP-binding sites and the impact of phosphorylation in cellular processes. Invest in the uncompromising quality and performance of this isomer for reliable, repeatable results in your investigative pursuits.