Cat. No. | Product Name | Target | Signaling Pathways |
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T79945 |
Ferroptosis-IN-1
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Ferroptosis | Apoptosis |
Ferroptosis-IN-1为弯草二萜类化合物,其抑制ferroptosis的EC50为10 μM,可用于神经炎症疾病研究。 | |||
T77762 |
ROS-generating agent 1
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Apoptosis; Ferroptosis; ROS Kinase | Apoptosis; Tyrosine Kinase/Adaptors |
ROS-generating agent 1 具有抗癌活性,通过共价修饰 TrxR 的 Sec-498 残基以生成 ROS。ROS-generating agent 1 降低细胞内 TrxR 蛋白水平,促进 NCI-H460 细胞中 ROS 依赖的性细胞凋亡 (apoptosis) 和铁死亡 (ferroptosis)。 | |||
T11631 |
iFSP1
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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。 | |||
T4309 |
CIL56
CA3 |
Ferroptosis; ROS | Apoptosis; Immunology/Inflammation |
CIL56 (CA3) 是一种选择性铁死亡诱导剂,可通过产生铁依赖性活性氧来诱导细胞铁死亡。 | |||
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。 | |||
T63729 |
GPX4-IN-3
|
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GPX4-IN-3 (26a) 作为一种有效的谷胱甘肽过氧化物酶4 (GPX4) 抑制剂,其能选择性诱导铁死亡(ferroptosis)。在1 μM浓度下,该化合物能抑制GPX4活性达71.7%。 | |||
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。 | |||
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 ... | |||
T79777 |
GPX4-IN-7
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Ferroptosis | Apoptosis |
GPX4-IN-7 (Compound 31),一种靛玉红衍生物,作为结肠癌铁死亡的诱导剂,对HCT-116细胞显示出卓越的抗肿瘤效果,IC50为0.49 μM。该化合物通过促进GPX4降解和脂质ROS积累,有效触发铁死亡。 | |||
T35994 |
Erastin2
Erastin2 |
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Erastin2 is a ferroptosis inducer and an inhibitor of the system xc- cystine/glutamate transporter.[1] [2] It inhibits glutamate release in CCF-STTG1 cells (IC50 = 0.0035 µM).[2] It induces cell death in HAP1 cells when used at a concentration of 5 µM, an effect that can be blocked by the ferroptosis inhibitor ferrostatin-1 or deferoxamine . [1] Erastin2 also induces ferroptotic cell death in HT-1080 cells (EC50 = 0.15 µM), an effect that can be blocked by the reducing agent β-merc... | |||
T37851 |
Chlorido[N,N'-disalicylidene-1,2-phenylenediamine]iron(III)
|
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Chlorido[N,N'-disalicylidene-1,2-phenylenediamine]iron(III) is an inducer of ferroptosis.1 It induces ferroptosis, but not apoptosis or necroptosis, in NB1 cancer cells when used at a concentration of 3 μM.1 Chlorido[N,N'-disalicylidene-1,2-phenylenediamine]iron(III) inhibits proliferation of BJAB, NALM-6, Jurkat, MelHO, and MCF-7 cancer cells (IC50s = 0.07, 2.5, 1.5, 3, and 5 μM, respectively), as well as NALM-6 cells resistant to daunorubicin and vincristine when used at concentrations ranging... | |||
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... | |||
T80847 | W1131 TFA | STAT | JAK/STAT signaling; Stem Cells |
W1131 TFA 是一种抑制STAT3并诱导铁死亡(ferroptosis)的有效化合物。在胃癌的皮下异种移植模型、类器官模型以及PDX模型中,它都能显著阻止疾病的发展。此外,W1131能有效缓解癌细胞对5-FU的化学耐药性。该化合物还通过调节IL6-JAK-STAT3和铁死亡(ferroptosis)通路来影响细胞周期、DNA损伤响应和氧化磷酸化过程。 | |||
T80052 |
Cathepsin B
|
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Cathepsin B为一种半胱氨酸蛋白酶,涉及多种程序性细胞死亡(包括细胞凋亡、焦亡、铁亡、坏死亡及自噬性细胞死亡)。 | |||
T36616 |
DTUN
|
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DTUN is a lipophilic hyponitrite radical initiator.1It initiates co-autoxidation of STY-BODIPY-embedded egg phosphatidylcholine liposomes when used at a concentration of 0.2 mM. DTUN has been used in fluorescence-enabled inhibited autoxidation (FENIX) assays for the development of ferroptosis inhibitors and the study of antioxidants in lipid membranes.1,2 1.Shah, R., Farmer, L.A., Zilka, O., et al.Beyond DPPH: Use of fluorescence-enabled inhibited autoxidation to predict oxidative cell death res... | |||
T73558 | W1131 | ||
W1131 是一种有效的STAT3抑制剂,可引发铁死亡。W1131 在胃癌皮下异种移植模型、类器官模型和 PDX 模型中抑制癌症进展。W1131 有效减轻癌细胞对 5-FU 化学耐药性。W1131 调节细胞周期、DNA 损伤反应和氧化磷酸化,包括IL6-JAK-STAT3通路和铁死亡 (ferroptosis) 通路。 | |||
T79359 | Anticancer agent 147 | Ferroptosis | Apoptosis |
Anticanceragent 147(化合物6j),作为槐定碱的衍生物,功能为铁死亡(Ferroptosis)诱导剂。该化合物能促进Fe2+、活性氧(ROS)及丙二醛(MDA)在细胞内的积累,并通过增加内质网(ER)应激和上调转录因子ATF3的表达发挥作用。在体外及体内实验中,Anticanceragent 147展现了出色的抗肝癌活性。 | |||
T36003 | 1(R)-(Trifluoromethyl)oleyl alcohol | ||
1(R)-(Trifluoromethyl)oleyl alcohol is an analog of oleic acid .1It inhibits ferroptosis induced by erastin in primary fibroblasts isolated from patients with Friedreich ataxia, a neuro- and cardiodegenerative disorder characterized by loss or impaired activity of frataxin (FXN), when used at concentrations of 5, 10, or 20 μM. 1(R)-(Trifluoromethyl)oleyl alcohol (5 μM) reduces lipid peroxidation induced byFXNsiRNA knockdown in NBT human myoblasts. 1.Cotticelli, M.G., Forestieri, R., Xia, S., et ... | |||
T37248 |
Pantothenate Kinase Inhibitor
|
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Pantothenate Kinase Inhibitor (PANKi) is a reversible inhibitor of pantothenate kinase (PanK; IC50s = 70, 92, and 25 nM for PanK1β, PanK2, and PanK3, respectively), the rate-limiting enzyme in the synthesis of coenzyme A .1It binds to the ATP-PanK3 complex with an apparent binding constant of 300 nM and exhibits mixed-type inhibition with respect to ATP and pantothenate. PANKi inhibits CoA biosynthesis in C3A cells (IC50= 0.9 μM) with no effect on cell viability when used at concentrations up to... | |||
T37805 |
JKE-1716
|
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JKE-1716 is an inhibitor of glutathione peroxidase 4 (GPX4) and a derivative of the GPX4 inhibitor ML-210 .1JKE-1716 reduces viability of LOX-IMVI cancer cells in a concentration-dependent manner and in a panel of additional cancer cell lines, an effect that can be blocked by the ferroptosis inhibitor ferrostatin-1 . 1.Eaton, J.K., Furst, L., Ruberto, R.A., et al.Selective covalent targeting of GPX4 using masked nitrile-oxide electrophilesNat. Chem. Biol.16(5)497-506(2020) | |||
T79042 | RIP1 kinase inhibitor 5 | RIP kinase | Apoptosis; NF-κB |
RIP1 kinase inhibitor 5 (example 1) 为一RIP1抑制剂,作为肿瘤免疫检查点激酶应用,与 SIR1-365 (compound 13) 类似,具有抑制坏死 (necrosis) 与铁死亡活性。 | |||
T83886 |
icFSP1 TFA
|
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icFSP1是一种抑制剂,针对的是铁死亡抑制蛋白1(FSP1)。在2.5 µM的浓度下使用时,能够引发FSP1在细胞中的凝聚和相分离,但在无细胞测试中并不抑制FSP1的酶活性(IC50 = > 30 µM)。icFSP1以浓度依赖的方式诱导HT-1080纤维肉瘤细胞的铁死亡。在体内,icFSP1(50 mg/kg)通过使用人类过表达FSP1,Gpx4-/-Fsp1-/-的B16/F10细胞,在B16/F10鼠黑色素瘤模型中减少肿瘤体积和重量。 | |||
T79638 | Lepadin E | Glutathione Peroxidase | Metabolism |
Lepadin E 是一种铁死亡(ferroptosis)诱导剂,它通过激活 p53-SLC7A11-GPX4 途径显著诱发细胞毒性。该化合物增强 p53 的表达,减少 SLC7A11 及 GPX4 的水平,进而导致活性氧 (ROS) 和脂质过氧化物的增加,并通过上调 ACSL4 来促进细胞死亡。Lepadin E 还具有显著的抗肿瘤效果。 | |||
T81823 |
Mem-C1C18
|
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Mem-C1C18是极性敏感荧光探针,具优质膜锚定性与高亮度,可通过荧光寿命变化响应环境极性。适用于铁死亡过程中质膜极性变化定量检测。 | |||
T83871 |
Ferroptocide
|
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Ferroptocide是一种抑制剂,可抑制硫氧还蛋白(Trx)活性,并且是pleuromutilin的衍生物。在20 µM的浓度下,Ferroptocide能够抑制ES-2卵巢癌细胞中的Trx活性,并对ES-2细胞具有细胞毒性(IC50 = 1.6 µM)。5 µM的Ferroptocide能够诱导ES-2细胞发生铁死亡,这一效应可以通过铁螯合剂去铁胺(DFO)、抗氧化剂Trolox或铁死亡抑制剂ferrostatin-1来阻断。在使用免疫完整但非免疫缺陷小鼠的4T1小鼠乳腺癌模型中,每周两次以50 mg/kg剂量给药时,Ferroptocide能够减少肿瘤体积。 | |||
T74763 | PAA5 | ||
PAA5为以甲基化物碳中心的多核Au(I)簇,能释放Au(I)促进氧化反应,加速铁死亡,并以时间依赖性方式提高pH2AX表达,表现出抗癌活性。 | |||
T36882 |
CAY10773
|
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CAY10773 is a derivative of the ferroptosis inducer sorafenib .1It selectively inhibits proliferation of BEL-7402, MGC803, and T24 bladder cancer cells (IC50s = 5.77, 5.21 and 3.97 μM, respectively) over non-cancerous HCV-29 cells (IC50= 23.19 μM). CAY10773 induces apoptosis in T24 cells when used at concentrations ranging from 2 to 6 μM but induces ferroptosis at concentrations greater than or equal to 6 μM with 10 hour or longer incubation times. It increases the production of reactive oxygen ... | |||
T74461 | Chalcones A-N-5 | ||
ChalconesA-N-5, 一种三羟基查耳酮衍生物化合物,浓度低于100 µM (IC50> 1 mM) 时无细胞毒性,能显着促进细胞增殖。此外,ChalconesA-N-5 能促进受损脑组织中神经元的生长,抑制RSL或erastin诱导的铁死亡,并降低Aβ1-42蛋白聚集引发的脂质过氧化水平。因此,ChalconesA-N-5 作为分子骨架的候选物,对于开发用以研究AD的体内试验先导化合物具有重要潜力。 | |||
T36504 |
STY-BODIPY
STY-BODIPY,Styrene-BODIPY |
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STY-BODIPY is a styrene-conjugated fluorogenic probe for radical-trapping antioxidant (RTA) activity.1 Co-autoxidation of the STY-BODIPY signal carrier and a hydrocarbon co-substrate can be quantified by monitoring the loss of absorbance at 571 nm. STY-BODIPY has been used to measure the activity of RTAs, as well as the kinetics and stoichiometry of RTA reactions in cell-free assays.1,2,3References1. Haidasz, E.A., Van Kessel, A.T.M., and Pratt, D.A. A continuous visible light spectrophotometric... |