Benfotiamine

CAS No. 22457-89-2

Benfotiamine( Benzoylthiamine monophosphate )

Catalog No. M13604 CAS No. 22457-89-2

Benfotiamine, the lipid-soluble thiamine derivative used as a treatment for diabetic neuropathy.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 83 In Stock
100MG 31 In Stock
200MG 45 In Stock
500MG 73 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Benfotiamine
  • Note
    Research use only, not for human use.
  • Brief Description
    Benfotiamine, the lipid-soluble thiamine derivative used as a treatment for diabetic neuropathy.
  • Description
    Benfotiamine, the lipid-soluble thiamine derivative used as a treatment for diabetic neuropathy, can inhibit three major pathways(the hexosamine pathway, the advanced glycation end product (AGE) formation pathway and the diacylglycerol (DAG)protein kinase C (PKC) pathway)of hyperglycemic damage and prevent experimental diabetic retinopathy. Benfotiamine is a synthetic S-acyl derivative of thiamine (vitamin B1) for treating sciatica and other painful nerve conditions. More effective at increasing thiamin levels in blood and tissues than water-soluble salts like the previous vitamin B1.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Benzoylthiamine monophosphate
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    22457-89-2
  • Formula Weight
    466.46
  • Molecular Formula
    C19H23N4O6PS
  • Purity
    >98% (HPLC)
  • Solubility
    Soluble in DMSO
  • SMILES
    O=C(S/C(CCOP(O)(O)=O)=C(N(CC1=CN=C(C)N=C1N)C=O)/C)C2=CC=CC=C2
  • Chemical Name
    (Z)-S-(2-(N-((4-amino-2-methylpyrimidin-5-yl)methyl)formamido)-5-(phosphonooxy)pent-2-en-3-yl) benzothioate

Shipping & Storage Information

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

Reference

1.Bozic I, et al. PLoS One. 2015 Feb 19;10(2):e0118372.
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