2'(3')-O-(4-Benzoylbenzoyl)adenosine 5'-triphosphate triethylammonium salt

93%

  • Product Code: 76773
  CAS:    112898-15-4
Molecular Weight: 715.39 (anhydrous free acid basis) g./mol Molecular Formula: C₂₄H₂₄N₆O₁₆P₃C₆H₁₆NH₂O
EC Number: MDL Number: MFCD00058547
Melting Point: Boiling Point:
Density: Storage Condition: −20°C
Product Description: This compound is widely used in biochemical research, particularly in studies involving ATP-dependent processes. It serves as a photoreactive ATP analog, enabling the investigation of ATP-binding proteins and enzymes. The benzoylbenzoyl group allows for UV-induced cross-linking, making it a valuable tool for identifying and characterizing ATP-binding sites in proteins. It is also employed in mechanistic studies of ATPases, kinases, and other ATP-utilizing enzymes, providing insights into their function and regulation. Additionally, it is utilized in photoaffinity labeling experiments to study protein-ligand interactions and map active sites. Its applications extend to understanding cellular energy metabolism and signal transduction pathways.
Product Specification:
Test Specification
APPEARANCE White to Off-White Powder
PURITY 92.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.005 10-20 days $294.93
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2'(3')-O-(4-Benzoylbenzoyl)adenosine 5'-triphosphate triethylammonium salt
This compound is widely used in biochemical research, particularly in studies involving ATP-dependent processes. It serves as a photoreactive ATP analog, enabling the investigation of ATP-binding proteins and enzymes. The benzoylbenzoyl group allows for UV-induced cross-linking, making it a valuable tool for identifying and characterizing ATP-binding sites in proteins. It is also employed in mechanistic studies of ATPases, kinases, and other ATP-utilizing enzymes, providing insights into their function and regulation. Additionally, it is utilized in photoaffinity labeling experiments to study protein-ligand interactions and map active sites. Its applications extend to understanding cellular energy metabolism and signal transduction pathways.
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