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
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Biological Information

  • Product Name
    Cyclic N-Acetyl-D-mannosamine
  • Note
    Research use only, not for human use.
  • Brief Description
    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.
  • Description
    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.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    2-ACETAMIDO-2-DEOXY-D-MANNOPYRANOSE HYDRATE
  • Pathway
    Proteasome/Ubiquitin
  • Target
    Endogenous Metabolite
  • Recptor
    others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    7772-94-3
  • Formula Weight
    221.21
  • Molecular Formula
    C8H15NO6
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 5 mg/mL;Water: 5 mg/mL
  • SMILES
    CC(=O)N[C@@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • 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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