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 | £222.33 |
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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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