Cyclic N-Acetyl-D-mannosamine
CAS No. 7772-94-3
Cyclic N-Acetyl-D-mannosamine( 2-ACETAMIDO-2-DEOXY-D-MANNOPYRANOSE HYDRATE )
Catalog No. M19663 CAS No. 7772-94-3
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.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | 37 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameCyclic N-Acetyl-D-mannosamine
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NoteResearch use only, not for human use.
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Brief DescriptionN-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.
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DescriptionN-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.
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In Vitro——
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In Vivo——
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Synonyms2-ACETAMIDO-2-DEOXY-D-MANNOPYRANOSE HYDRATE
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PathwayProteasome/Ubiquitin
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TargetEndogenous Metabolite
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Recptorothers
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Research Area——
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Indication——
Chemical Information
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CAS Number7772-94-3
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Formula Weight221.21
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Molecular FormulaC8H15NO6
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Purity>98% (HPLC)
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SolubilityDMSO: 5 mg/mL;Water: 5 mg/mL
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SMILESCC(=O)N[C@@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Sreekumar A et al.Metabolomic profiles delineate potential role for sarcosine in prostate cancer progression.Nature. 2009 Feb 12;457(7231):910-4. doi: 10.1038/nature07762.
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