Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3646 |
RSL3
RSL3 1S,1S,3R-RSL3 |
Ferroptosis; GPX; Glutathione Peroxidase | Apoptosis; Metabolism; oxidation-reduction |
RSL3 (RSL3 1S) 是一种 GPX4 的抑制剂,抑制阻断 GSH 合成的 system xc- (IC50=100 nM)。RSL3 是一种不依赖 VDAC 的铁死亡激活剂,对携带致癌 RAS 的肿瘤细胞具有选择性。 | |||
T41203 |
1R,3R-RSL3
1R,3R-RSL3 |
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1R,3R-RSL3 is a negative control for1S, 3R-RSL3. | |||
T11631 |
iFSP1
|
Ferroptosis | Apoptosis |
iFSP1 是一种强效、选择性和谷胱甘肽独立的铁死亡抑制蛋白 1 (FSP1) (AIFM2) 抑制剂,具有EC50 为 103 nM。它能够使多种人类癌细胞系对铁死亡诱导剂敏感,例如 (1S,3R)-RSL3。它在过表达 FSP1 的 GPX4 敲除细胞中选择性地诱导铁死亡。 | |||
T2376 |
Liproxstatin-1
|
Ferroptosis | Apoptosis |
Liproxstatin-1 是一种铁死亡抑制剂 (IC50=22 nM),具有强效性和选择性。Liproxstatin-1 可以保护细胞免受铁死亡诱导剂 (如 Erastin、RSL3) 诱导的铁死亡。 | |||
T79294 |
NC-R17
|
Glutathione Peroxidase | Metabolism |
NC-R17是一种衍生自RSL3的非共价GPX4降解剂,涉及铁死亡(Ferroptosis)过程。该化合物展现出抗肿瘤活性,用于非共价GPX4 PROTAC的设计。 | |||
T82408 | Ferroptosis-IN-3 | Ferroptosis | Apoptosis |
Ferroptosis-IN-3(Compound 25)是一款抑制RSL3引起的铁死亡(HT-1080细胞中EC50为8.6nM)的铁死亡抑制剂。此外,Ferroptosis-IN-3能有效清除DPPH和ABTS自由基(EC50分别为3.94μM与6.3μM),并且能降低脂质过氧化水平。 | |||
T37487 |
1-Stearoyl-2-15(S)-HpETE-sn-glycero-3-PE
|
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1-Stearoyl-2-15(S)-HpETE-sn-glycero-3-PE is a phospholipid that contains stearic acid at the sn-1 position and 15(S)-HpETE at the sn-2 position. It is produced via oxidation of 1-stearoyl-2-arachidonoyl-sn-glycero-3-PE by 15-lipoxygenase (15-LO). 1-Stearoyl-2-15(S)-HpETE-sn-glycero-3-PE (0.6 and 0.9 μM) increases ferroptotic cell death in wild-type and Acsl4 knockout Pfa1 mouse embryonic fibroblasts (MEFs) treated with the GPX4 inhibitor RSL3. | |||
T36516 |
RC574
RC574 |
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RC574 is an inhibitor of ferroptosis and a derivative of the antioxidant and hypocholesterolemic agent probucol .1It inhibits glutamate-induced cell death in HT22 cells (IC50= 276.2 nM) and mouse primary cortical neurons when used at a concentration of 3 μM. RC574 (3 μM) increases glutathione peroxidase 1 (GPX1) levels and GPX activity, as well as inhibits glutamate-induced mitochondrial superoxide anion production, in HT22 cells. It completely inhibits ferroptosis induced by the GPX4 inhibitor ... | |||
T83780 |
GPX4 24
Phospholipid Hydroperoxide Glutathione Peroxidase 24,PHGPx 24,Glutathione Peroxidase 4 24 |
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GPX4 24是(1S,3R)-RSL3的衍生物,具有抑制谷胱甘肽过氧化物酶4(GPX4)的作用。它能够在浓度依赖的方式中与4T1小鼠乳腺癌细胞中的GPX4形成共价结合。在GPX4依赖的HT-1080成纤维细胞中,GPX4 24诱导铁死亡(EC50 = 0.16 µM)。当以200 mg/kg剂量给予小鼠时,它能够增加小鼠肾脏和血浆中丙二醛(MDA)的水平。 | |||
T36515 | RC363 | ||
RC363 is an inhibitor of ferroptosis and a derivative of the antioxidant and hypocholesterolemic agent probucol .1It reduces 2,2-diphenyl-1-picrylhydrazyl radicals by approximately 40% in a cell-free assay when used at a concentration of 25 μM. RC363 prevents glutamate-induced toxicity in HT22 cultured hippocampal cells (IC50= 234.5 nM) but does not reduce oxidant levels in these cells. It increases the levels of glutathione peroxidase 1 (GPX1) and the activity of GPX in glutamate-challenged HT2... |