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  2. Nicotinamide - Wikipedia

    en.wikipedia.org/wiki/Nicotinamide

    Side effects are minimal. [7] [8] At high doses, liver problems may occur. [7] Normal amounts are safe for use during pregnancy. [9] Nicotinamide is in the vitamin B family of medications, specifically the vitamin B 3 complex. [10] [11] It is an amide of nicotinic acid. [7] Foods that contain nicotinamide include yeast, meat, milk, and green ...

  3. Nicotinic acid - Wikipedia

    en.wikipedia.org/wiki/Nicotinic_acid

    Nicotinic acid was first synthesized in 1867 by oxidative degradation of nicotine with potassium chromate and sulfuric acid [63] — this is the origin of the name. [16] Nicotinic acid is prepared by hydrolysis of nicotinonitrile, which, as described above, is generated by oxidation of 3

  4. Vitamin B3 - Wikipedia

    en.wikipedia.org/wiki/Vitamin_B3

    Although nicotinic acid and nicotinamide are identical in their vitamin activity, nicotinamide does not have the same pharmacological, lipid-modifying effects or side effects as nicotinic acid, i.e., when nicotinic acid takes on the -amide group, it does not reduce cholesterol nor cause flushing.

  5. Nicotine - Wikipedia

    en.wikipedia.org/wiki/Nicotine

    The reaction now proceeds via the NAD salvage cycle to produce nicotinic acid via the conversion of nicotinamide by the enzyme nicotinamidase. [ citation needed ] The N -methyl-Δ 1 -pyrrollidium cation used in the synthesis of nicotine is an intermediate in the synthesis of tropane-derived alkaloids.

  6. Inositol nicotinate - Wikipedia

    en.wikipedia.org/wiki/Inositol_nicotinate

    Inositol nicotinate is generally safe when taken by mouth, but possible side effects include: Stomach upset; Intestinal gas; Nausea; Liver damage (similar to other niacin products) [1] It is marketed as "no-flush" niacin, but research suggests that the lack of flushing may be due to its limited conversion to active niacin. [4]

  7. Nicotinamide riboside - Wikipedia

    en.wikipedia.org/wiki/Nicotinamide_riboside

    Nicotinamide riboside (NR) is now known to be an NAD+ precursor, involved in the biosynthetic pathways that convert B3 vitamins into NAD+. NAD+ is primarily synthesized in mammals de novo from tryptophan, through the Priess-Handler pathway from nicotinic acid (NA) or via a salvage pathway from nicotinamide (NAM).

  8. Nicotinamide mononucleotide - Wikipedia

    en.wikipedia.org/wiki/Nicotinamide_mononucleotide

    Nicotinamide mononucleotide ("NMN" and "β-NMN") is a nucleotide derived from ribose, nicotinamide, nicotinamide riboside and niacin. [1] In humans, several enzymes use NMN to generate nicotinamide adenine dinucleotide (NADH). [1]

  9. 1-Methylnicotinamide - Wikipedia

    en.wikipedia.org/wiki/1-Methylnicotinamide

    1-Methylnicotinamide (1-MNA, trigonellamide) is a prototypic organic cation. [1] 1-Methylnicotinamide is the methylated amide of Nicotinamide (niacinamide, vitamin B 3).1-Methylnicotinamide is an endogenic substance that is produced in the liver when Nicotinamide is metabolized.