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Home  > Adenosine 5'-(trihydrogen diphosphate), 3'-(dihydrogen phosphate), P'→5'-ester with 3-acetyl-1-β-D-ribofuranosylpyridinium, inner salt, disodium salt (9CI)

AA08092

102029-67-4 | Adenosine 5'-(trihydrogen diphosphate), 3'-(dihydrogen phosphate), P'→5'-ester with 3-acetyl-1-β-D-ribofuranosylpyridinium, inner salt, disodium salt (9CI)

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Description
Catalog Number: AA08092
Chemical Name: Adenosine 5'-(trihydrogen diphosphate), 3'-(dihydrogen phosphate), P'→5'-ester with 3-acetyl-1-β-D-ribofuranosylpyridinium, inner salt, disodium salt (9CI)
CAS Number: 102029-67-4
Molecular Formula: C22H30N6NaO17P3+
Molecular Weight: 766.4147
MDL Number: MFCD00078837
SMILES: OC1C(COP(=O)(OP(=O)(OCC2OC(C(C2OP(=O)(O)O)O)n2cnc3c2ncnc3N)O)O)OC(C1O)[n+]1cccc(c1)C(=O)C.[Na]

 

Upstream Synthesis Route
  • 3-Acetylpyridine adenine dinucleotide phosphate sodium salt, also known as AcPyADP-Na, is a crucial cofactor and redox-active compound used in various chemical synthesis processes. With its ability to transfer high-energy electrons in enzymatic reactions, this compound plays a vital role in biochemistry and biotechnology applications.In chemical synthesis, 3-Acetylpyridine adenine dinucleotide phosphate sodium salt serves as a cofactor in enzymatic reactions, where it facilitates the transfer of acetyl groups and electrons between different substrates. This enables the conversion of various molecules, such as aldehydes and ketones, through redox reactions and acetylation processes.Furthermore, AcPyADP-Na is commonly utilized in the synthesis of pharmaceutical compounds, organic chemicals, and bioactive molecules. Its unique properties make it a valuable tool in the development of novel drugs, fine chemicals, and biochemical research.Overall, the application of 3-Acetylpyridine adenine dinucleotide phosphate sodium salt in chemical synthesis allows for efficient and selective transformations of organic compounds, contributing to advancements in the field of chemistry and biotechnology.
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