Norfluoxetine Hydrochloride

CAS No. 57226-68-3

Norfluoxetine Hydrochloride ( Norfluoxetine HCl )

Catalog No. M27362 CAS No. 57226-68-3

Norfluoxetine hydrochloride is an active metabolite of fluoxetine. Fluoxetine is an antidepressant drug.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 149 Get Quote
10MG 217 Get Quote
25MG 357 Get Quote
50MG 475 Get Quote
100MG 689 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Norfluoxetine Hydrochloride
  • Note
    Research use only, not for human use.
  • Brief Description
    Norfluoxetine hydrochloride is an active metabolite of fluoxetine. Fluoxetine is an antidepressant drug.
  • Description
    Norfluoxetine hydrochloride is an active metabolite of fluoxetine. Fluoxetine is an antidepressant drug.
  • Synonyms
    Norfluoxetine HCl
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    tyrosine hydroxylase (TH)
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    57226-68-3
  • Formula Weight
    331.8
  • Molecular Formula
    C16H17ClF3NO
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    Cl.NCCC(Oc1ccc(cc1)C(F)(F)F)c1ccccc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Luck LA, et al. Fluorescence and 19F NMR evidence that phenylalanine, 3-L-fluorophenylalanine and 4-L-fluorophenylalanine bind to the L-leucine specific receptor of Escherichia coli. Protein Sci. 2000;9(12):2573-2576.
molnova catalog
related products
  • m-Toluoyl chloride

    m-Toluoyl chloride is a bioactive chemical.

  • PF-06952229

    PF-06952229 is an selective and orally active inhibitor of TGFbR1.

  • Bacterial Sortase Su...

    Bacterial Substrate III, Abz/DNP TFA is an internally quenched fluorescent peptide substrate. Staphylococcus aureus transpeptidase sortase A (SrtA) reacts with its native substrate Bacterial Sortase Substrate III, Abz/DNP, cleaving it and catalyzing the formation of an amide bond between the carboxyl group of threonine and the amino group of cell-wall crossbridges.