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Raw Materials
Ferroptosis
Chemical Structure | Cat. No. | Product Name | CAS No. |
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BCP37001 | iFSP1 New | 150651-39-1 |
iFSP1 is a ferroptosis suppressor protein 1 (FSP1) inhibitor and ferroptosis inducer.
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BCP34023 | Donafenib New | 1130115-44-4 |
Donafenib is an oral multikinase inhibitor that targets Raf kinase and receptor tyrosine kinases with potential anticancer acivity. Donafenib is under clinical trials in China in patients with advanced hepatocellular carcinoma (HCC).
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BCP31858 | Imidazole ketone erastin New | 1801530-11-9 |
Imidazole ketone erastin (IKE), is a potent, metabolically stable inhibitor of system xc- and inducer of ferroptosis potentially suitable for in vivo applications.
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BCP30942 | UAMC-3203 hydrochloride New | 2271358-65-5 |
UAMC-3203 hydrochloride is a potent and selective Ferroptosis inhibitor with an IC50 of 12 nM.
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BCP12825 | Tinoridine | 24237-54-5 |
Tinoridine, also known as Y-3642, is a non-steroidal anti-inflammatory drug.
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BCP30905 | Tinoridine hydrochloride New | 25913-34-2 |
Tinoridine hydrochloride is a nonsteroidal anti-inflammatory drug and also has potent radical scavenger and antiperoxidative activity.
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BCP20203 | PF-06282999 | 1435467-37-0 |
PF-06282999 is a potent and selective myeloperoxidase inhibitor which is potential useful for the treatment of cardiovascular diseases.
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BCP30847 | Verdiperstat New | 890655-80-8 |
Verdiperstat (AZD3241) is a selective, irreversible and orally active myeloperoxidase inhibitor, with an IC50 of 630 nM, and can be used in the research of neurodegenerative brain disorders.
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BCP30685 | UAMC3203 3HCl New | UAMC32033HCl |
UAMC-3203 is a novel potent, drug-like ferroptosis inhibitor with IC50 of 12 nM, inhibit erastin-induced ferroptotic cell death more potently than Ferrostatin-1; shows an improved protection compared to Fer-1 against multi-organ injury in mice, represents novel lead compounds with therapeutic potential in relevant ferroptosis-driven disease models.
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BCP30684 | UAMC-3203 New | 2271358-64-4 |
UAMC-3203 is a potent and selective Ferroptosis inhibitor with an IC50 of 12 nM.
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