Fumonisin B1

CAS No. 116355-83-0

Fumonisin B1( ——— )

Catalog No. M38015 CAS No. 116355-83-0

Fumonisin B1 is a mycotoxin produced from Fusarium moniliforme. Fumonisin B1 is a potent inhibitor of sphingosine N-acyltransferase (ceramide synthase) and disrupts de novo sphingolipid biosynthesis.Fumonisin B1 is the most abundant and toxic fumonisin.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG Get Quote Get Quote
50MG Get Quote Get Quote
100MG Get Quote Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Fumonisin B1
  • Note
    Research use only, not for human use.
  • Brief Description
    Fumonisin B1 is a mycotoxin produced from Fusarium moniliforme. Fumonisin B1 is a potent inhibitor of sphingosine N-acyltransferase (ceramide synthase) and disrupts de novo sphingolipid biosynthesis.Fumonisin B1 is the most abundant and toxic fumonisin.
  • Description
    Fumonisin B1 is a mycotoxin produced from Fusarium moniliforme.
  • In Vitro
    ———
  • In Vivo
    ———
  • Synonyms
    ———
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Sphingosine N-acyltransferase
  • Research Area
    ———
  • Indication
    ———

Chemical Information

  • CAS Number
    116355-83-0
  • Formula Weight
    721.83
  • Molecular Formula
    C34H59NO15
  • Purity
    >98% (HPLC)
  • Solubility
    H2O : 16.67 mg/mL (23.09 mM)
  • SMILES
    O.CCCC[C@@H](C)[C@@H](OC(=O)C[C@@H](CC(O)=O)C(O)=O)C(C[C@@H](C)C[C@H](O)CCCC[C@@H](O)C[C@H](O)[C@H](C)N)OC(=O)C[C@@H](CC(O)=O)C(O)=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Henry MH, et al. The toxicity of fumonisin B1, B2, and B3, individually and in combination, in chicken embryos. Poult Sci. 2001 Apr;80(4):401-7.?
molnova catalog
related products
  • Licoflavonol

    Licoflavonol is a novel natural inhibitor of Salmonella T3SS, could be a promising candidate for novel type of anti-virulence drugs, it exhibits a strong inhibitory effect on the secretion of the SPI-1 effector proteins via regulating the transcription of the SicA/InvF genes, and the transportation of the effector protein SipC.

  • HAE

    HAE is a 3-amino acid peptide composed of histidine, alanine and glutamate.

  • Benzquinamide hydroc...

    Benzquinamide hydrochloride is an antiemetic agent and increases intra-arterial pressure due to the increased peripheral vascular resistance.