General Information of MET (ID: META00304) |
Name |
1-Methylnicotinamide
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Synonyms |
Click to Show/Hide Synonyms of This Metabolite
1-Methyl-3-carbamoylpyridinium; 1-Methyl-3-carbamoylpyridinium cation; 1-Methylnicotinamide cation; 3-(Aminocarbonyl)-1-methylpyridinium; 3-Amido-N-methylpyridinium: 1-methyl-3-pyridinecarboxamide; 3-Carbamoyl-1-methyl-pyridinium; I-methyl nicotinamide', N'-methylnicotinamide, N'Methylnicotinamide, 'N-1-Methylnicotinamide; N(1)-Methylnicotinamide; N(1)-Methylnicotinamide bromide; N(1)-Methylnicotinamide chloride; N(1)-Methylnicotinamide cyanide; N(1)-Methylnicotinamide fluoride; N(1)-Methylnicotinamide iodide; N(1)-Methylnicotinamide iodide, 3-(aminocarbonyl-13C)-labeled; N(1)-Methylnicotinamide methylsulfate; N(1)-Methylnicotinamide perchlorate; N(1)-Methylnicotinamide tetrafluoroborate (1-); N-Methyl-3-carbamidopyridinium; N-Methyl-3-carbamoylpyridinium ion; N1-Methylnicotinamide; Trigonellamide chloride; Trigonellinamide
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Source |
Endogenous;Escherichia Coli Metabolite;Yeast Metabolite;Food;Microbial
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Structure Type |
Pyridinecarboxylic acids and derivatives (Click to Show/Hide the Complete Structure Type Hierarchy)
Organoheterocyclic compounds
Pyridines and derivatives
Pyridinecarboxylic acids and derivatives
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PubChem CID |
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HMDB ID |
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Formula |
C7H9N2O
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Structure |
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3D MOL
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2D MOL
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Click to Show/Hide the Molecular/Functional Data (External Links/Property/Function) of This Metabolite
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KEGG ID |
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DrugBank ID |
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ChEBI ID |
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FooDB ID |
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ChemSpider ID |
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METLIN ID |
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Physicochemical Properties |
Molecular Weight |
137.16 |
Topological Polar Surface Area |
47 |
XlogP |
-0.1 |
Complexity |
136 |
Heavy Atom Count |
10 |
Rotatable Bond Count |
1 |
Hydrogen Bond Donor Count |
1 |
Hydrogen Bond Acceptor Count |
1 |
Function |
1-Methylnicotinamide is a metabolite of nicotinamide and is produced primarily in the liver. It has anti-inflammatory properties. It is a product of nicotinamide N-methyltransferase [EC 2.1.1.1] in the pathway of nicotinate and nicotinamide metabolism (KEGG). 1-Methylnicotinamide may be an endogenous activator of prostacyclin production and thus may regulate thrombotic as well as inflammatory processes in the cardiovascular system.
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Regulatory Network
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