Niacin
Sugar
Banking Soda
Methyl (Me)
-CH3
Bicarbonate Ion
CHO3-
..
Osmolyte
Methyl Donor
Methylated
One-Carbon
Buffered Niacin
Niacin Inositol
Trigonelline
Preiss-Handler Pathway
(NaPRT)
Nicotinic Acid
Phosphoribosyltransferase
Ocean Marine Nitrogen
Dinitrogen
A New NAD+ Precursor More Stable than NMN and NR: Trigonelline
https://www.nad.com/news/a-new-nad-precursor-more-stable-than-nmn-and-nr-trigonelline
How is NAD+ Made? Preiss-Handler Pathway
https://www.qualialife.com/how-is-nad-made-preiss-handler-pathway
..
Vitamin B3: Metabolism and Functions
https://themedicalbiochemistrypage.org/vitamin-b3-metabolism-and-functions/
Methylation Donor: Roles in One-Carbon Metabolism and Health
https://biologyinsights.com/methylation-donor-roles-in-one-carbon-metabolism-and-health/
..
Trigonelline
most basic Nitrogen compound found in plants.
Dinitrogen
most basic Nitrogen compound found in Ocean Marine & Atmosphere
..
Methyl
Methyl Radical
Methenium (Cation)
..
Glutamine
vs
Glutamate
Melatonin
vs
Serotonin
..
Nitrotyrosine
Peroxynitrite
vs
NAC
https://en.m.wikipedia.org/wiki/Nitrotyrosine
https://en.m.wikipedia.org/wiki/Sodium_benzoate
..
Phosphorus-Nitrogen Heterocycles Derived from Chelating N-Donor Ligands
https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202404420
..
Niacin
DMSO
Nitrogen
Heterocycles
Hexanicotinate
Quinazoline
Keratinocyte
Nuclear Factor Erythroid 2-Related Factor 2 (NRF2)
Phosphorus-Nitrogen Heterocycles Derived from Chelating N-Donor Ligands:
https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202404420
Seeing red: flushing out instigators of niacin-associated skin toxicity
https://pmc.ncbi.nlm.nih.gov/articles/PMC2912206/
NRF2 Activation by Nitrogen Heterocycles
https://pmc.ncbi.nlm.nih.gov/articles/PMC10058096/
Quinazolinones, the Winning Horse in Drug Discovery
https://pmc.ncbi.nlm.nih.gov/articles/PMC9919317/
Organocatalyzed Synthesis of Quinazolines
https://www.chemistryviews.org/details/ezine/11218877/Organocatalyzed_Synthesis_of_Quinazolines/
organocatalytic protocol for the synthesis of diversely substituted quinazolines promoted by vitamin B3 (niacin), using nitriles as a CN source. The team used various 2-aminobenzylamines and nitriles as substrates, niacin as the catalyst, and dimethylsulfoxide (DMSO) as the solvent. The reaction was performed at 110 °C under air.