| General Information of MET (ID: META00805) |
| Name |
N-Acetylmannosamine
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| Synonyms |
Click to Show/Hide Synonyms of This Metabolite
2-Acetamido-2-deoxy-D-mannopyranose; 2-Acetamido-2-deoxy-D-mannose; ManNAc; N-Acetyl-D-mannosamine; N-Acetyl-beta-mannosamine; N-Acetylmannosamine, (D)-isomer; N-Acetylmannosamine, (L)-isomer; beta-ManNAc
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| Source |
Endogenous;Escherichia Coli Metabolite;Food
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| Structure Type |
Carbohydrates and carbohydrate conjugates (Click to Show/Hide the Complete Structure Type Hierarchy)
Organic oxygen compounds
Organooxygen compounds
Carbohydrates and carbohydrate conjugates
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| PubChem CID |
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| HMDB ID |
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| Formula |
C8H15NO6
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| Structure |
<iframe style="width: 300px; height: 300px;" frameborder="0" src="https://embed.molview.org/v1/?mode=balls&cid=11096158"></iframe>
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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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| 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 |
221.21 |
Topological Polar Surface Area |
119 |
| XlogP |
-1.7 |
Complexity |
235 |
| Heavy Atom Count |
15 |
Rotatable Bond Count |
2 |
| Hydrogen Bond Donor Count |
5 |
Hydrogen Bond Acceptor Count |
6 |
| Function |
N-Acetylmannosamine is a monosaccharide that is used as a precursor in the chemical or enzymatic synthesis of the neuraminic acids found in glycolipids and glycoproteins. N-Acetyl-D-mannosamine (ManNAc) is a specific substrate for the synthesis of N-acetylneuraminic acid, the essential precursor of bacterial capsular polysialic acid (PA). N-Acetyl-D-mannosamine is used for the synthesis of sialic acid. It is also a synthetic intermediate for a number of carbohydrate-derived families of biologically active compounds and pharmaceutical candidates. N-Acetylmannosamine is a microbial metabolite of Escherichia.
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Regulatory Network
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Induced Change