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VIT-2763

Chemical Structure : VIT-2763

CAS No.: 2095668-10-1

VIT-2763 (Vamifeport, VIT2763)

Catalog No.: PC-73101Not For Human Use, Lab Use Only.

VIT-2763 (Vamifeport, VIT2763) is an oral small molecule inhibitor of ferroportin, inhibits hepcidin binding to ferroportin with IC50 of 9 nM, blocks iron efflux.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

VIT-2763 (Vamifeport, VIT2763) is an oral small molecule inhibitor of ferroportin, inhibits hepcidin binding to ferroportin with IC50 of 9 nM, blocks iron efflux.
VIT-2763 triggers ubiquitination and subsequent internalization and degradation of ferroportin.
Orally dosed VIT-2763 (30 mg/kg) decreased decrease in serum iron induced by hepcidin in rodents.
VIT-2763 decreased serum iron and prevented liver iron loading in Hbbth3/+ mice.
VIT-2763 significantly corrected anemia and improved RBC parameters in Hbbth3/+ mice, improved the ineffective erythropoiesis in BM and spleen.
VIT-2763 reduced the formation of insoluble α-globin aggregates and improved the elimination of mitochondria in RBCs.
VIT-2763 decreased apoptosis and extended the life span, reduced hypoxia response of RBCs.

Physicochemical Properties

M.Wt 408.437
Formula C21H21FN6O2
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

2-(2-((2-(1H-benzo[d]imidazol-2-yl)ethyl)amino)ethyl)-N-((3-fluoropyridin-2-yl)methyl)oxazole-4-carboxamide

References

1. Manolova V, et al. J Clin Invest. 2019 Dec 9;130(1):491-506.

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