Chemical Structure : NCOA4-FTH1 inhibitor 9a
CAS No.: 2650557-72-3
货号: 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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---|---|---|---|
5 mg | ¥2880 | In stock | |
10 mg | ¥4480 | In stock | |
25 mg | ¥7580 | In stock | |
50 mg | Get quote | ||
100 mg | Get quote |
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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).
分子量 | 441.55 | |
分子式 | C27H28FN5 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
6-Fluoro-1,2,3,4-tetrahydro-2-[3-[6-(4-methyl-1-piperazinyl)-1H-benzimidazol-2-yl]phenyl]isoquinoline |
1. Fang Y, et al. ACS Cent Sci. 2021 Jun 23;7(6):980-989.
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