Substance

ID:182481

3-Acetylpyridine adenine dinucleotide

Names and Identifiers
IUPAC Traditional name
3-acetyl-1-[(2R,3R,4S,5R)-5-[({[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy(hydroxy)phosphoryl phosphonato}oxy)methyl]-3,4-dihydroxyoxolan-2-yl]-1λ5-pyridin-1-ylium
IUPAC name
3-acetyl-1-[(2R,3R,4S,5R)-5-{[({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl phosphonato)oxy]methyl}-3,4-dihydroxyoxolan-2-yl]-1λ5-pyridin-1-ylium
Synonyms
APAD3-Acetylpyridine adenine dinucleotide
Registration numbers
MDL Number
PubChem SID
CAS Number
Properties
Safety Information
Storage Temperature
-20°C
GHS Pictograms
GHS07
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Risk Statements
36/37/38
European Hazard Symbols
Irritant Irritant (Xi)
GHS Signal Word
Warning
GHS Precautionary statements
P261-P305+P351+P338
GHS Hazard statements
H315-H319-H335
Safety Statements
26
German water hazard class
3
Product Information
Purity
≥85%
Molecule Details
Biochem/physiol Actions
APAD is an NAD analog with higher oxidation potential than NAD. It can substitute for NAD as a hydrogen-accepting cofactor in many dehydrogenase reactions; e.g. lactate dehydrogenase from Toxoplasma, Clonorchis, and Plasmodium, bacterial lipoamide dehydrogenase, as well as mammalian dehydrogenases. It can also act as a proton acceptor in various transhydrogenation reactions with NADH or NADPH.
Linkage
Analog of NAD
Molecular Spectra
No Data Available
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References
No Data Available
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