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NCOA4-FTH1 inhibitor 9a

Chemical Structure : NCOA4-FTH1 inhibitor 9a

CAS No.: 2650557-72-3

NCOA4-FTH1 inhibitor 9a

Catalog No.: PC-22833Not For Human Use, Lab Use Only.

NCOA4-FTH1 inhibitor 9a is a new ferroptosis inhibitor through disrupting the NCOA4-FTH1 protein-protein interaction, reduces intracellular ferrous iron, inhibits Erastin-induced ferroptosiswith EC50 of 0.29 μM in HT22 cells.

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

Biological Activity

NCOA4-FTH1 inhibitor 9a is a new ferroptosis inhibitor through disrupting the NCOA4-FTH1 protein-protein interaction, reduces intracellular ferrous iron, inhibits Erastin-induced ferroptosiswith EC50 of 0.29 μM in HT22 cells.
NCOA4-FTH1 inhibitor 9a directly binds to recombinant protein NCOA4383–522 (Kd=7.48 uM) and effectively blocks the NCOA4383–522–FTH1 interaction.
NCOA4-FTH1 inhibitor 9a significantly ameliorates the ischemic-refusion injury in rat model of ischemic stroke.
NCOA4-FTH1 inhibitor 9a is a selective ferroptosis inhibitor that effectively suppresses lipid peroxidation and rescues cells from ferroptosis.
NCOA4-FTH1 inhibitor 9a inhibits lysosomal ferritin degradation and localizes in autophagosomes. effectively blocks RSL3-induced ferroptosis in HT22 cells (EC50 = 3.66 μM).

Physicochemical Properties

M.Wt 441.55
Formula C27H28FN5
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

6-Fluoro-1,2,3,4-tetrahydro-2-[3-[6-(4-methyl-1-piperazinyl)-1H-benzimidazol-2-yl]phenyl]isoquinoline

References

1. Fang Y, et al. ACS Cent Sci. 2021 Jun 23;7(6):980-989.

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