|M10244||Imidazole ketone erastin||Imidazole ketone erastin (IKE) is an inducer of ferroptosis, and it is also a potent, selective, and metabolically stable inhibitor of the cystine-glutamate antiporter, system Xc-.|
|M9404||UAMC-3203 hydrochloride||UAMC-3203 hydrochloride is a potent and selective Ferroptosis inhibitor, with an IC50 of 12 nM.|
|M9060||RSL3||RSL3 is an inhibitor of the glutathione (GSH) peroxidase 4, which can inhibit the cysteine/glutamate amino acid transporter system.|
|M8531||Liproxstatin-1||Liproxstatin-1 is a potent inhibitor of ferroptosis, a non-apoptotic form of cell death characterized by iron-dependent accumulation of lethal lipid reactive oxygen species (ROS).|
|M7504||CIL56 (CA3)||CIL56 (CA3) is a potent and selective ferroptosis inducer, it has potent inhibitory effects on YAP1/Tead transcriptional activity and primarily targets YAP1 high and therapy-resistant esophageal adenocarcinoma cells endowed with CSC properties.|
|M6731||FIN56||FIN56 is a ferroptosis activator.|
|M5558||Deferoxamine mesylate||Deferoxamine mesylate as a chelating agent used to remove excess iron from the body.|
|M3400||Idebenone||Idebenone is a synthetic analog of coenzyme Q10 (CoQ10) and a brain stimulant.|
|M2698||Ferrostatin-1||Ferrostatin-1 (Fer-1) is a potent and selective inhibitor of ferroptosis with EC50 of 60 nM.|
|M2679||Erastin||Erastin is a ferroptosis activator by acting on mitochondrial VDAC, exhibiting selectivity for tumor cells bearing oncogenic RAS. *The compound is unstable in solutions, freshly prepared is recommended|
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