Methyl α-D-mannopyranoside

CAS No. 617-04-9

Methyl α-D-mannopyranoside( Methyl α-D-mannopyranoside? )

Catalog No. M27563 CAS No. 617-04-9

Methyl α-D-mannopyranoside can be used as an intermediate for chemical sythesis and can target macrophages in anti-tuberculosis inhalation therapy.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 28 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G 31 In Stock

Biological Information

  • Product Name
    Methyl α-D-mannopyranoside
  • Note
    Research use only, not for human use.
  • Brief Description
    Methyl α-D-mannopyranoside can be used as an intermediate for chemical sythesis and can target macrophages in anti-tuberculosis inhalation therapy.
  • Description
    Methyl α-D-mannopyranoside can be used as an intermediate for chemical sythesis and can target macrophages in anti-tuberculosis inhalation therapy.(In Vivo):Methyl α-D-mannopyranoside, a competitor inhibitor of the binding of mannose by Escherichia coli, was tested for its ability to prevent infection of the urinary tract of mice with infective strains of the organisms.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Methyl α-D-mannopyranoside?
  • Pathway
    GPCR/G Protein
  • Target
    Antibacterial
  • Recptor
    RSV
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    617-04-9
  • Formula Weight
    194.183
  • Molecular Formula
    C7H14O6
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?H2O : ≥ 100 mg/mL (514.99 mM))
  • SMILES
    COC1OC(CO)C(O)C(O)C1O
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Y C Chen, et al. Inhibition of Nitric Oxide Synthase Inhibitors and Lipopolysaccharide Induced Inducible NOS and cyclooxygenase-2 Gene Expressions by Rutin, Quercetin, and Quercetin Pentaacetate in RAW 264.7 Macrophages. J Cell Biochem. 2001;82(4):537-48.
molnova catalog
related products
  • PBP 10

    Selective formyl peptide receptor 2 (FPR2) antagonist; cell permeable. Selectively inhibits FPR2-mediated NADPH oxidase activity but has no effect on FPR1 signaling in neutrophils. Displays PIP2 binding activity in vitro and blocks cell motility. Also exhibits antiviral activity against influenza viruses via inhibition of viral-induced ERK activation.

  • Carabrone

    Carabrone, a botanical bicyclic sesquiterpenic lactone, is a promising fungicidal agent that can effectively control G. tritici.

  • Cefodizime

    Cefodizime is a new cephalosporin antibiotic with a wide range of biological activities.Cefodizime is non-toxic to the kidneys and is well tolerated with immunomodulatory activity.