Nicotinamide riboside malate

Catalog No.: A56966
Endogenous Metabolite
Nicotinamide riboside malate is an endogenous metabolite that acts as an orally active precursor of NAD+. This compound is known to elevate NAD+ levels and activate sirtuin enzymes SIRT1 and SIRT3, playing a crucial role in enhancing oxidative metabolism. Additionally, nicotinamide riboside malate has demonstrated protective effects against metabolic disorders induced by high-fat diets and mitigates cognitive decline in transgenic mouse models of Alzheimer’s disease. It serves as a valuable tool for research into metabolic health and neurodegeneration.
Grouped product items
Size Price Stock Qty
100mg
$45.00
In stock
500mg
$70.00
In stock
1g
$90.00
In stock
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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
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Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
DescriptionNicotinamide riboside malate is an endogenous metabolite that acts as an orally active precursor of NAD+. This compound is known to elevate NAD+ levels and activate sirtuin enzymes SIRT1 and SIRT3, playing a crucial role in enhancing oxidative metabolism. Additionally, nicotinamide riboside malate has demonstrated protective effects against metabolic disorders induced by high-fat diets and mitigates cognitive decline in transgenic mouse models of Alzheimer’s disease. It serves as a valuable tool for research into metabolic health and neurodegeneration.
Product Information
Catalog NumA56966
FormulaC15H20N2O10
Molecular Weight388.33
CAS Number2415659-01-5
SMILESNC(C1=C[N+]([C@H]2[C@@H]([C@@H]([C@H](O2)CO)O)O)=CC=C1)=O.O[C@H](C(O)=O)CC([O-])=O
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