| Identification | Back Directory | [Name]
3-ACETYLPYRIDINE ADENINE DINUCLEOTIDE | [CAS]
86-08-8 | [Synonyms]
APAD
3-ACETYLPYRIDINE NAD
acetyldiphosphopyridine nucleotide
3-ACETYLPYRIDINE ADENINE DINUCLEOTIDE
3-ACETYLPYRIDINE ADENINE DINUCLEOTIDE, REDUCED FORM
3-Acetylpyridine hypoxanthine dinucleotide，oxidized form
3-Acetylpyridine adenine dinucleotide, oxidised form 92+%
5'-ester with 3-acetyl-1-b-D-ribofuranosylpyridinium, inner salt
3-Acetyl-1-((2R,3R,4S,5R)-5-((((((((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)(hydroxy)phosphoryl)oxy)oxidophosphoryl)oxy)methyl)-3,4-dihydroxytetrahydrofuran-2-yl)pyridin-1-ium | [EINECS(EC#)]
201-649-4 | [Molecular Formula]
C22H28N6O14P2 | [MDL Number]
MFCD00078882 | [MOL File]
86-08-8.mol | [Molecular Weight]
662.44 |
| Hazard Information | Back Directory | [Description]
3-Acetylpyridine NAD (APAD) is an analog of NAD+ (free acid) (nicotinamide adenine dinucleotide; ), a signaling molecule and cofactor or substrate for many enzymes. APAD has been used to study the mechanisms of oxidative phosphorylation. It can be reduced by transdehydrogenase from NADH (sodium salt) . It can be reduced more efficiently and is more stable than NAD+; thus, it is useful as a substitute. | [Definition]
ChEBI: 3-acetylpyridine adenine dinucleotide is an organic molecular entity. |
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