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Results for "

hepcidin production

" in TargetMol Product Catalog.
  • Inhibitors & Agonists
    5
    TargetMol | All_Pathways
  • Peptide Products
    1
    TargetMol | Peptide_Products
  • Oligonucleotides
    2
    TargetMol | All_Pathways
  • DS28120313
    T151702146177-09-3
    DS28120313 is an oral inhibitor of hepcidin production (IC50: 0.093 μM).
    • $854
    6-8 weeks
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  • Zilurgisertib fumarate
    INCB-000928 fumarate, ,NBU-928 fumarate
    T848602173390-30-0
    Zilurgisertib fumarate (INB-000928 fumarate) is a potent and selective inhibitor of Activin Receptor-Like Kinase 2 (ALK2/ACVR1). It significantly inhibits ALK2 kinase activity (IC50 = 15 nM) and downregulates BMP-6-induced SMAD1/5 phosphorylation (IC50 = 63 nM). By blocking ALK2-mediated signaling, Zilurgisertib suppresses the production of hepcidin in hepatocytes (IC50 = 20 nM), thereby modulating iron metabolism. In preclinical studies, Zilurgisertib demonstrates the potential to improve anemia in cancer-induced models by effectively increasing hemoglobin levels.
    • $189
    In Stock
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  • Sapablursen
    ISIS 702843, IONIS-TMPRSS6-Lrx
    T2174212273007-95-5
    Sapablursen is an antisense oligonucleotide that reduces the production of TMPRSS6, thereby increasing serum hepcidin levels. Serum hepcidin is a crucial regulator of iron homeostasis. Sapablursen can be used in studies of hematological disorders, such as polycythemia vera.
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  • Sapablursen sodium
    ISIS 702843 sodium, IONIS-TMPRSS6-Lrx sodium
    T2174382273008-00-5
    Sapablursen sodium is an antisense oligonucleotide that reduces the production of TMPRSS6, leading to increased expression of serum hepcidin, which is a key regulator of iron homeostasis. Sapablursen may be used in research on blood disorders such as polycythemia vera.
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  • Rusfertide
    PTG-300
    TP26181628323-80-7
    Rusfertide, a peptide mimetic of natural hepcidin, targets and degrades ferroportin, thereby reducing serum iron and transferrin saturation, which helps regulate red blood cell production. It ameliorates conditions such as polycythemia vera, β-thalassemia, and hereditary hemochromatosis [1] [2].
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