Nicotinamide riboside

Catalog No.: A56989
SIRT1/3 Activator
Nicotinamide riboside is an orally active NAD+ precursor that functions as an activator of SIRT1 and SIRT3. This compound elevates NAD+ levels, enhances oxidative metabolism, and provides protective effects against metabolic abnormalities induced by high-fat diets. Additionally, nicotinamide riboside has been shown to mitigate cognitive decline in transgenic mouse models of Alzheimer’s disease, making it a valuable reagent for research in metabolism and neurodegenerative disorders.
Grouped product items
Size Price Stock Qty
5mg
$40.00
In stock
200mg
$185.00
In stock
Bulk Size
Bulk Discount
Free Delivery on orders over $500
Research use only. We do not sell to patients.

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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
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 is an orally active NAD+ precursor that functions as an activator of SIRT1 and SIRT3. This compound elevates NAD+ levels, enhances oxidative metabolism, and provides protective effects against metabolic abnormalities induced by high-fat diets. Additionally, nicotinamide riboside has been shown to mitigate cognitive decline in transgenic mouse models of Alzheimer’s disease, making it a valuable reagent for research in metabolism and neurodegenerative disorders.
Product Information
Catalog NumA56989
FormulaC11H15N2O5
Molecular Weight255.25
CAS Number1341-23-7
SMILESNC(C1=C[N+]([C@H]2[C@@H]([C@@H]([C@H](O2)CO)O)O)=CC=C1)=O
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